CROSSREFERENCE TO RELATED APPLICATIONS This application is a continuation of copending U.S. Pat. Application No. 16/438,819, filed on Jun. 12, 2019, which is a continuation of U.S. Pat. Application No. 15/240,044, filed on Aug. 18, 2016, which claims priority to U.S. Provisional applications No. 62/213,757, filed on Sep. 3, 2015; No. 62/232,194, filed on Sep. 24, 2015; No. 62/291,960, filed on Feb. 5, 2016; No. 62/322,510, filed on Apr. 14, 2016; and No. 62/330,412 filed on May 2, 2016, the entire contents of which are incorporated herein by reference.
PARTIES TO A JOINT RESEARCH AGREEMENT The claimed invention was made by, on behalf of, and/or in connection with one or more of the following parties to a joint university corporation research agreement: The Regents of the University of Michigan, Princeton University, University of Southern California, and the Universal Display Corporation. The agreement was in effect on and before the date the claimed invention was made, and the claimed invention was made as a result of activities undertaken within the scope of the agreement.
FIELD The present invention relates to compounds for use as emitters, and devices, such as organic light emitting diodes, including the same.
BACKGROUND Optoelectronic devices that make use of organic materials are becoming increasingly desirable for a number of reasons. Many of the materials used to make such devices are relatively inexpensive, so organic optoelectronic devices have the potential for cost advantages over inorganic devices. In addition, the inherent properties of organic materials, such as their flexibility, may make them well suited for particular applications such as fabrication on a flexible substrate. Examples of organic optoelectronic devices include organic light emitting diodes/devices (OLEDs), organic phototransistors, organic photovoltaic cells, and organic photodetectors. For OLEDs, the organic materials may have performance advantages over conventional materials. For example, the wavelength at which an organic emissive layer emits light may generally be readily tuned with appropriate dopants.
OLEDs make use of thin organic films that emit light when voltage is applied across the device. OLEDs are becoming an increasingly interesting technology for use in applications such as flat panel displays, illumination, and backlighting. Several OLED materials and configurations are described in U.S. Pat. Nos. 5,844,363, 6,303,238, and 5,707,745, which are incorporated herein by reference in their entirety.
One application for phosphorescent emissive molecules is a full color display. Industry standards for such a display call for pixels adapted to emit particular colors, referred to as “saturated” colors. In particular, these standards call for saturated red, green, and blue pixels. Alternatively the OLED can be designed to emit white light. In conventional liquid crystal displays emission from a white backlight is filtered using absorption filters to produce red, green and blue emission. The same technique can also be used with OLEDs.The white OLED can be either a single EML device or a stack structure. Color may be measured using CIE coordinates, which are well known to the art.
One example of a green emissive molecule is tris(2phenylpyridine) iridium, denoted Ir(ppy)_{3}, which has the following structure:
In this, and later figures herein, we depict the dative bond from nitrogen to metal (here, Ir) as a straight line.
As used herein, the term “organic” includes polymeric materials as well as small molecule organic materials that may be used to fabricate organic optoelectronic devices. “Small molecule” refers to any organic material that is not a polymer, and “small molecules” may actually be quite large. Small molecules may include repeat units in some circumstances. For example, using a long chain alkyl group as a substituent does not remove a molecule from the “small molecule” class. Small molecules may also be incorporated into polymers, for example as a pendent group on a polymer backbone or as a part of the backbone. Small molecules may also serve as the core moiety of a dendrimer, which consists of a series of chemical shells built on the core moiety. The core moiety of a dendrimer may be a fluorescent or phosphorescent small molecule emitter. A dendrimer may be a “small molecule,” and it is believed that all dendrimers currently used in the field of OLEDs are small molecules.
As used herein, “top” means furthest away from the substrate, while “bottom” means closest to the substrate. Where a first layer is described as “disposed over” a second layer, the first layer is disposed further away from substrate. There may be other layers between the first and second layer, unless it is specified that the first layer is “in contact with” the second layer. For example, a cathode may be described as “disposed over” an anode, even though there are various organic layers in between.
As used herein, “solution processible” means capable of being dissolved, dispersed, or transported in and/or deposited from a liquid medium, either in solution or suspension form.
A ligand may be referred to as “photoactive” when it is believed that the ligand directly contributes to the photoactive properties of an emissive material. A ligand may be referred to as “ancillary” when it is believed that the ligand does not contribute to the photoactive properties of an emissive material, although an ancillary ligand may alter the properties of a photoactive ligand.
As used herein, and as would be generally understood by one skilled in the art, a first “Highest Occupied Molecular Orbital” (HOMO) or “Lowest Unoccupied Molecular Orbital” (LUMO) energy level is “greater than” or “higher than” a second HOMO or LUMO energy level if the first energy level is closer to the vacuum energy level. Since ionization potentials (IP) are measured as a negative energy relative to a vacuum level, a higher HOMO energy level corresponds to an IP having a smaller absolute value (an IP that is less negative). Similarly, a higher LUMO energy level corresponds to an electron affinity (EA) having a smaller absolute value (an EA that is less negative). On a conventional energy level diagram, with the vacuum level at the top, the LUMO energy level of a material is higher than the HOMO energy level of the same material. A “higher” HOMO or LUMO energy level appears closer to the top of such a diagram than a “lower” HOMO or LUMO energy level.
As used herein, and as would be generally understood by one skilled in the art, a first work function is “greater than” or “higher than” a second work function if the first work function has a higher absolute value. Because work functions are generally measured as negative numbers relative to vacuum level, this means that a “higher” work function is more negative. On a conventional energy level diagram, with the vacuum level at the top, a “higher” work function is illustrated as further away from the vacuum level in the downward direction. Thus, the definitions of HOMO and LUMO energy levels follow a different convention than work functions.
More details on OLEDs, and the definitions described above, can be found in U.S. Pat. No. 7,279,704, which is incorporated herein by reference in its entirety.
SUMMARY According to one embodiment, a composition comprising a first compound is provided. In the composition, the first compound is capable of functioning as a phosphorescent emitter in an organic light emitting device at room temperature, and the first compound has at least one aromatic ring and at least one substituent R, where each of the at least one substituent R is directly bonded to one of the at least one aromatic rings. Each of the at least one substituent R has the formula of
where :
 (a) G^{1} is selected from the group consisting of NR^{1}, SiR^{1}R^{2}, GeR^{1}R^{2}, alkyl, cycloalkyl, and combinations thereof; and G^{2} is a nonaromatic polycyclic group, which can be further substituted by one or more R^{3};
 (b) G^{1} is a direct bond; and G^{2} is a nonaromatic spiro polycyclic group, which can be further substituted by one or more R^{3}; or
 (c) G^{1} is selected from the group consisting of: direct bond, NR^{1}, SiR^{1}R^{2}, GeR^{1}R^{2}, alkyl, cycloalkyl, and combinations thereof; G^{2} is a nonaromatic polycyclic group, which can be further substituted by one or more R^{3}; and R is directly bonded to an aromatic ring selected from the group consisting of phenyl, pyridine, and triazine, which can be further fused to other rings;
 R^{1}, R^{2}, and R^{3} are independently selected from the group consisting of hydrogen, deuterium, halide, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acids, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof; and
 each G^{1} and G^{2} can be independently, partially or fully deuterated.
According to another embodiment, an organic light emitting diode/device (OLED) is also provided. The OLED can include an anode, a cathode, and an organic layer, disposed between the anode and the cathode. The organic layer can include the first compound as described herein. According to yet another embodiment, the organic light emitting device is incorporated into one or more device selected from a consumer product, an electronic component module, and/or a lighting panel.
According to yet another embodiment, a formulation containing the first compound as described herein is provided.
BRIEF DESCRIPTION OF THE DRAWINGS FIG. 1 shows an organic light emitting device.
FIG. 2 shows an inverted organic light emitting device that does not have a separate electron transport layer.
DETAILED DESCRIPTION Generally, an OLED comprises at least one organic layer disposed between and electrically connected to an anode and a cathode. When a current is applied, the anode injects holes and the cathode injects electrons into the organic layer(s). The injected holes and electrons each migrate toward the oppositely charged electrode. When an electron and hole localize on the same molecule, an “exciton,” which is a localized electronhole pair having an excited energy state, is formed. Light is emitted when the exciton relaxes via a photoemissive mechanism. In some cases, the exciton may be localized on an excimer or an exciplex. Nonradiative mechanisms, such as thermal relaxation, may also occur, but are generally considered undesirable.
The initial OLEDs used emissive molecules that emitted light from their singlet states (“fluorescence”) as disclosed, for example, in U.S. Pat. No. 4,769,292, which is incorporated by reference in its entirety. Fluorescent emission generally occurs in a time frame of less than 10 nanoseconds.
More recently, OLEDs having emissive materials that emit light from triplet states (“phosphorescence”) have been demonstrated. Baldo et al., “Highly Efficient Phosphorescent Emission from Organic Electroluminescent Devices,” Nature, vol. 395, 151154, 1998; (“BaldoI”) and Baldo et al., “Very highefficiency green organic lightemitting devices based on electrophosphorescence,” Appl. Phys. Lett., vol. 75, No. 3, 46 (1999) (“BaldoII”), are incorporated by reference in their entireties. Phosphorescence is described in more detail in U.S. Pat. No. 7,279,704 at cols. 56, which are incorporated by reference.
FIG. 1 shows an organic light emitting device 100. The figures are not necessarily drawn to scale. Device 100 may include a substrate 110, an anode 115, a hole injection layer 120, a hole transport layer 125, an electron blocking layer 130, an emissive layer 135, a hole blocking layer 140, an electron transport layer 145, an electron injection layer 150, a protective layer 155, a cathode 160, and a barrier layer 170. Cathode 160 is a compound cathode having a first conductive layer 162 and a second conductive layer 164. Device 100 may be fabricated by depositing the layers described, in order. The properties and functions of these various layers, as well as example materials, are described in more detail in US 7,279,704 at cols. 610, which are incorporated by reference.
More examples for each of these layers are available. For example, a flexible and transparent substrateanode combination is disclosed in U.S. Pat. No. 5,844,363, which is incorporated by reference in its entirety. An example of a pdoped hole transport layer is mMTDATA doped with F_{4}TCNQ at a molar ratio of 50:1, as disclosed in U.S. Pat. Application Publication No. 2003/0230980, which is incorporated by reference in its entirety. Examples of emissive and host materials are disclosed in U.S. Pat. No. 6,303,238 to Thompson et al., which is incorporated by reference in its entirety. An example of an ndoped electron transport layer is BPhen doped with Li at a molar ratio of 1:1, as disclosed in U.S. Pat. Application Publication No. 2003/0230980, which is incorporated by reference in its entirety. U.S. Pat. Nos. 5,703,436 and 5,707,745, which are incorporated by reference in their entireties, disclose examples of cathodes including compound cathodes having a thin layer of metal such as Mg:Ag with an overlying transparent, electricallyconductive, sputterdeposited ITO layer. The theory and use of blocking layers is described in more detail in U.S. Pat. No. 6,097,147 and U.S. Pat. Application Publication No. 2003/0230980, which are incorporated by reference in their entireties. Examples of injection layers are provided in U.S. Pat. Application Publication No. 2004/0174116, which is incorporated by reference in its entirety. A description of protective layers may be found in U.S. Pat. Application Publication No. 2004/0174116, which is incorporated by reference in its entirety.
FIG. 2 shows an inverted OLED 200. The device includes a substrate 210, a cathode 215, an emissive layer 220, a hole transport layer 225, and an anode 230. Device 200 may be fabricated by depositing the layers described, in order. Because the most common OLED configuration has a cathode disposed over the anode, and device 200 has cathode 215 disposed under anode 230, device 200 may be referred to as an “inverted” OLED. Materials similar to those described with respect to device 100 may be used in the corresponding layers of device 200. FIG. 2 provides one example of how some layers may be omitted from the structure of device 100.
The simple layered structure illustrated in FIGS. 1 and 2 is provided by way of nonlimiting example, and it is understood that embodiments of the invention may be used in connection with a wide variety of other structures. The specific materials and structures described are exemplary in nature, and other materials and structures may be used. Functional OLEDs may be achieved by combining the various layers described in different ways, or layers may be omitted entirely, based on design, performance, and cost factors. Other layers not specifically described may also be included. Materials other than those specifically described may be used. Although many of the examples provided herein describe various layers as comprising a single material, it is understood that combinations of materials, such as a mixture of host and dopant, or more generally a mixture, may be used. Also, the layers may have various sublayers. The names given to the various layers herein are not intended to be strictly limiting. For example, in device 200, hole transport layer 225 transports holes and injects holes into emissive layer 220, and may be described as a hole transport layer or a hole injection layer. In one embodiment, an OLED may be described as having an “organic layer” disposed between a cathode and an anode. This organic layer may comprise a single layer, or may further comprise multiple layers of different organic materials as described, for example, with respect to FIGS. 1 and 2.
Structures and materials not specifically described may also be used, such as OLEDs comprised of polymeric materials (PLEDs) such as disclosed in U.S. Pat. No. 5,247,190 to Friend et al., which is incorporated by reference in its entirety. By way of further example, OLEDs having a single organic layer may be used. OLEDs may be stacked, for example as described in U.S. Pat. No. 5,707,745 to Forrest et al, which is incorporated by reference in its entirety. The OLED structure may deviate from the simple layered structure illustrated in FIGS. 1 and 2. For example, the substrate may include an angled reflective surface to improve outcoupling, such as a mesa structure as described in U.S. Pat. No. 6,091,195 to Forrest et al., and/or a pit structure as described in U.S. Pat. No. 5,834,893 to Bulovic et al., which are incorporated by reference in their entireties.
Unless otherwise specified, any of the layers of the various embodiments may be deposited by any suitable method. For the organic layers, preferred methods include thermal evaporation, inkjet, such as described in U.S. Pat. Nos. 6,013,982 and 6,087,196, which are incorporated by reference in their entireties, organic vapor phase deposition (OVPD), such as described in U.S. Pat. No. 6,337,102 to Forrest et al., which is incorporated by reference in its entirety, and deposition by organic vapor jet printing (OVJP), such as described in U.S. Pat. No. 7,431,968, which is incorporated by reference in its entirety. Other suitable deposition methods include spin coating and other solution based processes. Solution based processes are preferably carried out in nitrogen or an inert atmosphere. For the other layers, preferred methods include thermal evaporation. Preferred patterning methods include deposition through a mask, cold welding such as described in U.S. Pat. Nos. 6,294,398 and 6,468,819, which are incorporated by reference in their entireties, and patterning associated with some of the deposition methods such as inkjet and OVJD. Other methods may also be used. The materials to be deposited may be modified to make them compatible with a particular deposition method. For example, substituents such as alkyl and aryl groups, branched or unbranched, and preferably containing at least 3 carbons, may be used in small molecules to enhance their ability to undergo solution processing. Substituents having 20 carbons or more may be used, and 320 carbons is a preferred range. Materials with asymmetric structures may have better solution processibility than those having symmetric structures, because asymmetric materials may have a lower tendency to recrystallize. Dendrimer substituents may be used to enhance the ability of small molecules to undergo solution processing.
Devices fabricated in accordance with embodiments of the present invention may further optionally comprise a barrier layer. One purpose of the barrier layer is to protect the electrodes and organic layers from damaging exposure to harmful species in the environment including moisture, vapor and/or gases, etc. The barrier layer may be deposited over, under or next to a substrate, an electrode, or over any other parts of a device including an edge. The barrier layer may comprise a single layer, or multiple layers. The barrier layer may be formed by various known chemical vapor deposition techniques and may include compositions having a single phase as well as compositions having multiple phases. Any suitable material or combination of materials may be used for the barrier layer. The barrier layer may incorporate an inorganic or an organic compound or both. The preferred barrier layer comprises a mixture of a polymeric material and a nonpolymeric material as described in U.S. Pat. No. 7,968,146, PCT Pat. Application Nos. PCT/US2007/023098 and PCT/US2009/042829, which are herein incorporated by reference in their entireties. To be considered a “mixture”, the aforesaid polymeric and nonpolymeric materials comprising the barrier layer should be deposited under the same reaction conditions and/or at the same time. The weight ratio of polymeric to nonpolymeric material may be in the range of 95:5 to 5:95. The polymeric material and the nonpolymeric material may be created from the same precursor material. In one example, the mixture of a polymeric material and a nonpolymeric material consists essentially of polymeric silicon and inorganic silicon.
Devices fabricated in accordance with embodiments of the invention can be incorporated into a wide variety of electronic component modules (or units) that can be incorporated into a variety of electronic products or intermediate components. Examples of such electronic products or intermediate components include display screens, lighting devices such as discrete light source devices or lighting panels, etc. that can be utilized by the enduser product manufacturers. Such electronic component modules can optionally include the driving electronics and/or power source(s). Devices fabricated in accordance with embodiments of the invention can be incorporated into a wide variety of consumer products that have one or more of the electronic component modules (or units) incorporated therein. Such consumer products would include any kind of products that include one or more light source(s) and/or one or more of some type of visual displays. Some examples of such consumer products include flat panel displays, computer monitors, medical monitors, televisions, billboards, lights for interior or exterior illumination and/or signaling, headsup displays, fully or partially transparent displays, flexible displays, laser printers, telephones, cell phones, tablets, phablets, personal digital assistants (PDAs), wearable device, laptop computers, digital cameras, camcorders, viewfinders, microdisplays, 3D displays, vehicles, a large area wall, theater or stadium screen, or a sign. Various control mechanisms may be used to control devices fabricated in accordance with the present invention, including passive matrix and active matrix. Many of the devices are intended for use in a temperature range comfortable to humans, such as 18° C. to 30° C., and more preferably at room temperature (2025° C.), but could be used outside this temperature range, for example, from 40° C. to + 80° C.
The materials and structures described herein may have applications in devices other than OLEDs. For example, other optoelectronic devices such as organic solar cells and organic photodetectors may employ the materials and structures. More generally, organic devices, such as organic transistors, may employ the materials and structures.
In the field of organic chemistry, a polycyclic compound is an organic chemical featuring several closed rings of atoms, primarily carbon. These ring substructures comprises cycloalkanes, aromatics, and other ring types. They come in sizes of three atoms and upward, and in combinations of linkages that include tethering (such as in biaryls), fusing (edgetoedge, such as in anthracene and steroids), links via a single atom (such as in spiro compounds), and bridged cyclics such as adamantane. Though “poly” literally means “many”, in this context polycyclic includes smaller rings such as bicyclic, tricyclic, and tetracyclic.
The term “halo,” “halogen,” or “halide” as used herein includes fluorine, chlorine, bromine, and iodine.
The term “alkyl” as used herein contemplates both straight and branched chain alkyl radicals. Preferred alkyl groups are those containing from one to fifteen carbon atoms and includes methyl, ethyl, propyl, 1methylethyl, butyl, 1methylpropyl, 2methylpropyl, pentyl, 1methylbutyl, 2methylbutyl, 3methylbutyl, 1,1dimethylpropyl, 1,2dimethylpropyl, 2,2dimethylpropyl,and the like. Additionally, the alkyl group may be optionally substituted.
The term “cycloalkyl” as used herein contemplates cyclic alkyl radicals. Preferred cycloalkyl groups are those containing 3 to 10 ring carbon atoms and includes cyclopropyl, cyclopentyl, cyclohexyl, adamantyl, and the like. Additionally, the cycloalkyl group may be optionally substituted.
The term “alkenyl” as used herein contemplates both straight and branched chain alkene radicals. Preferred alkenyl groups are those containing two to fifteen carbon atoms. Additionally, the alkenyl group may be optionally substituted.
The term “alkynyl” as used herein contemplates both straight and branched chain alkyne radicals. Preferred alkynyl groups are those containing two to fifteen carbon atoms. Additionally, the alkynyl group may be optionally substituted.
The terms “aralkyl” or “arylalkyl” as used herein are used interchangeably and contemplate an alkyl group that has as a substituent an aromatic group. Additionally, the aralkyl group may be optionally substituted.
The term “heterocyclic group” as used herein contemplates aromatic and nonaromatic cyclic radicals. Heteroaromatic cyclic radicals also means heteroaryl. Preferred heterononaromatic cyclic groups are those containing 3 to 7 ring atoms which includes at least one hetero atom, and includes cyclic amines such as morpholino, piperdino, pyrrolidino, and the like, and cyclic ethers, such as tetrahydrofuran, tetrahydropyran, and the like. Additionally, the heterocyclic group may be optionally substituted.
The term “aryl” or “aromatic group” as used herein contemplates singlering groups and polycyclic ring systems. The polycyclic rings may have two or more rings in which two carbons are common to two adjoining rings (the rings are “fused”) wherein at least one of the rings is aromatic, e.g., the other rings can be cycloalkyls, cycloalkenyls, aryl, heterocycles, and/or heteroaryls. Preferred aryl groups are those containing six to thirty carbon atoms, preferably six to twenty carbon atoms, more preferably six to twelve carbon atoms. Especially preferred is an aryl group having six carbons, ten carbons or twelve carbons. Suitable aryl groups include phenyl, biphenyl, triphenyl, triphenylene, tetraphenylene, naphthalene, anthracene, phenalene, phenanthrene, fluorene, pyrene, chrysene, perylene, and azulene, preferably phenyl, biphenyl, triphenyl, triphenylene, fluorene, and naphthalene. Additionally, the aryl group may be optionally substituted.
The term “heteroaryl” as used herein contemplates singlering heteroaromatic groups that may include from one to five heteroatoms. The term heteroaryl also includes polycyclic heteroaromatic systems having two or more rings in which two atoms are common to two adjoining rings (the rings are “fused”) wherein at least one of the rings is a heteroaryl, e.g., the other rings can be cycloalkyls, cycloalkenyls, aryl, heterocycles, and/or heteroaryls. Preferred heteroaryl groups are those containing three to thirty carbon atoms, preferably three to twenty carbon atoms, more preferably three to twelve carbon atoms. Suitable heteroaryl groups include dibenzothiophene, dibenzofuran, dibenzoselenophene, furan, thiophene, benzofuran, benzothiophene, benzoselenophene, carbazole, indolocarbazole, pyridylindole, pyrrolodipyridine, pyrazole, imidazole, triazole, oxazole, thiazole, oxadiazole, oxatriazole, dioxazole, thiadiazole, pyridine, pyridazine, pyrimidine, pyrazine, triazine, oxazine, oxathiazine, oxadiazine, indole, benzimidazole, indazole, indoxazine, benzoxazole, benzisoxazole, benzothiazole, quinoline, isoquinoline, cinnoline, quinazoline, quinoxaline, naphthyridine, phthalazine, pteridine, xanthene, acridine, phenazine, phenothiazine, phenoxazine, benzofuropyridine, furodipyridine, benzothienopyridine, thienodipyridine, benzoselenophenopyridine, and selenophenodipyridine, preferably dibenzothiophene, dibenzofuran, dibenzoselenophene, carbazole, indolocarbazole, imidazole, pyridine, triazine, benzimidazole, 1,2azaborine, 1,3azaborine, 1,4azaborine, borazine, and azaanalogs thereof. Additionally, the heteroaryl group may be optionally substituted.
The alkyl, cycloalkyl, alkenyl, alkynyl, aralkyl, heterocyclic group, aryl, and heteroaryl may be unsubstituted or may be substituted with one or more substituents selected from the group consisting of deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, cyclic amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acid, ether, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof.
As used herein, “substituted” indicates that a substituent other than H is bonded to the relevant position, such as carbon. Thus, for example, where R^{1} is monosubstituted, then one R^{1} must be other than H. Similarly, where R^{1} is disubstituted, then two of R^{1} must be other than H. Similarly, where R^{1} is unsubstituted, R^{1} is hydrogen for all available positions.
The “aza” designation in the fragments described herein, i.e. azadibenzofuran, azadibenzothiophene, etc. means that one or more of the CH groups in the respective fragment can be replaced by a nitrogen atom, for example, and without any limitation, azatriphenylene encompasses both dibenzo[f,h]quinoxaline and dibenzo[f,h]quinoline. One of ordinary skill in the art can readily envision other nitrogen analogs of the azaderivatives described above, and all such analogs are intended to be encompassed by the terms as set forth herein.
It is to be understood that when a molecular fragment is described as being a substituent or otherwise attached to another moiety, its name may be written as if it were a fragment (e.g. phenyl, phenylene, naphthyl, dibenzofuryl) or as if it were the whole molecule (e.g. benzene, naphthalene, dibenzofuran). As used herein, these different ways of designating a substituent or attached fragment are considered to be equivalent.
According to one embodiment, a composition comprising a first compound is described. In the composition, the first compound is capable of functioning as a phosphorescent emitter in an organic light emitting device at room temperature, and the first compound has at least one aromatic ring and at least one substituent R, where each of the at least one substituent R is directly bonded to one of the at least one aromatic rings. Each of the at least one substituent R has the formula of
where :
 (a) G^{1} is selected from the group consisting of NR^{1}, SiR^{1}R^{2}, GeR^{1}R^{2}, alkyl, cycloalkyl, and combinations thereof; and G^{2} is a nonaromatic polycyclic group, which can be further substituted by one or more R^{3};
 (b) G^{1} is a direct bond; and G^{2} is a nonaromatic spiro polycyclic group, which can be further substituted by one or more R^{3}; or
 (c) G^{1} is selected from the group consisting of: direct bond, NR^{1}, SiR^{1}R^{2}, GeR^{1}R^{2}, alkyl, cycloalkyl, and combinations thereof; G^{2} is a nonaromatic polycyclic group, which can be further substituted by one or more R^{3}; and R is directly bonded to an aromatic ring selected from the group consisting of phenyl, pyridine, and triazine, which can be further fused to other rings;
 wherein R^{1}, R^{2}, and R^{3} are independently selected from the group consisting of hydrogen, deuterium, halide, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acids, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof; and
 each G^{1} and G^{2} can be independently, partially or fully deuterated.
In some embodiments, G^{1} is SiR^{1}R^{2}. In some embodiments, G^{1} is NR^{1}. In some embodiments, G^{1} is alkyl. In some such embodiments, G^{1} is selected from the gourp consisiting of divalent methyl, ethyl, propyl, and butyl. In some embodiments, G^{1} is fully or partially deuterated.
In some embodiments, G^{2} is polycyclic alkyl. In some embodiments, G^{2} is carborane. In some embodiments, G^{2} contains at least one heteroatom. In some embodiments, G^{2} includes at least one heterocyclic group.
In some embodiments, the first compound is capable of emitting light from a triplet excited state to a ground singlet state at room temperature.
In some embodiments, the first compound is a metal coordination complex having a metalcarbon bond. In some such embodiments, the metal is selected from the group consisting of Ir, Rh, Re, Ru, Os, Pt, Au, and Cu. In some such embodiments, the metal is Ir, while the metal is Pt is other embodiments.
In some embodiments, the first compound has the formula of M(L^{1})_{x}(L^{2})_{y}(L^{3})_{z}, where:
 L^{1}, L^{2} and L^{3} can be the same or different;
 x is 1, 2, or 3;
 y is 0, 1, or 2;
 z is 0, 1, or 2;
 x+y+z is the oxidation state of the metal M;
 L^{1}, L^{2} and L^{3} are each independently selected from the group consisting of:




















 , and

 each X^{1} to X^{17} are independently selected from the group consisting of carbon and nitrogen;
 X is selected from the group consisting of BR′, NR′, PR′, O, S, Se, C═O, S═O, SO_{2}, CR′R″, SiR′R″, and GeR′R″;
 each R′ and R″ is independently, optionally fused or joined to form a ring;
 each R_{a}, R_{b}, R_{c}, and R_{d} independently represents from mono substitution to the maximum possible number of substitutions, or no substitution;
 each R′, R″, R_{a}, R_{b}, R_{c}, and R_{d} is independently selected from the group consisting of hydrogen, deuterium, halide, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acids, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof;
 any two adjacent substitutents of R_{a}, R_{b}, R_{c}, and R_{d} are optionally fused or joined to form a ring or form a multidentate ligand; and
 at least one of the R_{a}, R_{b}, R_{c}, and R_{d} includes the at least one substituent R.
In some embodiments where the first compound has the structure M(L^{1})_{x}(L^{2})_{y}(L^{3})_{z}, the first compound has the formula of Ir(L^{1})_{2}(L^{2}). In some such embodiments, L^{1} has the formula selected from the group consisting of:
and
and L^{2} has the formula
In some such embodiments, L^{2} has the formula:
where:
 R_{e}, R_{f}, R_{h}, and R_{i} are independently selected from group consisting of alkyl, cycloalkyl, aryl, and heteroaryl;
 at least one of R_{e}, R_{f}, R_{h}, and R_{i} has at least two carbon atoms; and
 R_{g} is selected from group consisting of hydrogen, deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acid, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof.
In some embodiments where the first compound has the formula of Ir(L^{1})_{2}(L^{2}), ligands L^{1} and L^{2} are different and each independently selected from the group consisting of:
, and
In some embodiments where the first compound has the formula of Ir(L^{1})_{2}(L^{2}), ligands L^{1} and L^{2} are each independently selected from the group consisting of:
, and
In some embodiments where the first compound has the structure M(L^{1})_{x}(L^{2})_{y}(L^{3})_{z}, the first compound has the formula of Pt(L^{1})_{2} or Pt(L^{1})(L^{2}). In some embodiments where the first compound has the formula of Pt(L^{1})_{2} or Pt(L^{1})(L^{2}), one L^{1} is connected to the other L^{1} or L^{2} to form a tetradentate ligand.
In some embodiments where the first compound has the structure M(L^{1})_{x}(L^{2})_{y}(L^{3})_{z}, at least one of R_{a}, R_{b}, R_{c}, and R_{d} includes an alkyl or cycloalkyl group that is partially or fully deuterated.
In some embodiments, G^{2} is selected from the group consisting of:
In some embodiments, each of the at least one substituent R is independently selected from the group consisting of:
, and
In some embodiments where the first compound has the structure M(L^{1})_{x}(L^{2})_{y}(L^{3})_{z},, at least one of L^{1}, L^{2}, and L^{3} is selected from the group consisting of:
, and
In some embodiments where the first compound has the formula of Ir(L^{1})_{2}(L^{2}), ligands L^{1} and L^{2} are different and each independently selected from the group consisting of:
and
In some embodiments where the first compound has the formula of M(L^{1})_{x}(L^{2})_{y}(L^{3})_{z}, ligand L^{1} is L_{A} having the following structure:
selected from the group consisting of L_{A1} to L_{A2480} as listed below:
Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6} Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6}
L_{A1} R^{G1} H H H H H L_{A1241} CD_{3} H R^{G58} H H H
L_{A2} R^{G2} H H H H H L_{A1242} CD_{3} H R^{G59} H H H
L_{A3} R^{G3} H H H H H L_{A1243} CD_{3} H R^{G60} H H H
L_{A4} R^{G4} H H H H H L_{A1244} CD_{3} H R^{G61} H H H
Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6} Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6}
L_{A5} R^{G5} H H H H H L_{A1245} CD_{3} H R^{G62} H H H
L_{A6} R^{G6} H H H H H L_{A1246} CD_{3} H R^{G63} H H H
L_{A7} R^{G7} H H H H H L_{A1247} CD_{3} H R^{G64} H H H
L_{A8} R^{G8} H H H H H L_{A1248} CD_{3} H R^{G65} H H H
L_{A9} R^{G9} H H H H H L_{A1249} CD_{3} H R^{G66} H H H
L_{A10} R^{G10} H H H H H L_{A1250} CD_{3} H R^{G67} H H H
L_{A11} R^{G11} H H H H H L_{A1251} CD_{3} H R^{G68} H H H
L_{A12} R^{G12} H H H H H L_{A1252} CD_{3} H R^{G69} H H H
L_{A13} R^{G13} H H H H H L_{A1253} CD_{3} H R^{G70} H H H
L_{A14} R^{G14} H H H H H L_{A1254} CD_{3} H R^{G71} H H H
L_{A15} R^{G15} H H H H H L_{A1255} CD_{3} H R^{G72} H H H
L_{A16} R^{G16} H H H H H L_{A1256} CD_{3} H R^{G73} H H H
L_{A17} R^{G17} H H H H H L_{A1257} CD_{3} H R^{G74} H H H
L_{A18} R^{G18} H H H H H L_{A1258} CD_{3} H R^{G75} H H H
L_{A19} R^{G19} H H H H H L_{A1259} CD_{3} H R^{G76} H H H
L_{A20} R^{G20} H H H H H L_{A1260} CD_{3} H R^{G77} H H H
L_{A21} R^{G21} H H H H H L_{A1261} CD_{3} H R^{G78} H H H
L_{A22} R^{G22} H H H H H L_{A1262} CD_{3} H R^{G79} H H H
L_{A23} R^{G23} H H H H H L_{A1263} CD_{3} H R^{G80} H H H
L_{A24} R^{G24} H H H H H L_{A1264} CD_{3} H R^{G81} H H H
L_{A25} R^{G25} H H H H H L_{A1265} CD_{3} H R^{G82} H H H
L_{A26} R^{G26} H H H H H L_{A1266} CD_{3} H R^{G83} H H H
L_{A27} R^{G27} H H H H H L_{A1267} CD_{3} H R^{G84} H H H
L_{A28} R^{G28} H H H H H L_{A1268} CD_{3} H R^{G85} H H H
Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6} Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6}
L_{A29} R^{G29} H H H H H L_{A1269} CD_{3} H R^{G86} H H H
L_{A30} R^{G30} H H H H H L_{A1270} CD_{3} H R^{G87} H H H
L_{A31} R^{G31} H H H H H L_{A1271} CD_{3} H R^{G88} H H H
L_{A32} R^{G32} H H H H H L_{A1272} CD_{3} H R^{G89} H H H
L_{A33} R^{G33} H H H H H L_{A1273} CD_{3} H R^{G90} H H H
L_{A34} R^{G34} H H H H H L_{A1274} CD_{3} H R^{G91} H H H
L_{A35} R^{G35} H H H H H L_{A1275} CD_{3} H R^{G92} H H H
L_{A36} R^{G36} H H H H H L_{A1276} CD_{3} H R^{G93} H H H
L_{A37} R^{G37} H H H H H L_{A1277} CD_{3} H R^{G94} H H H
L_{A38} R^{G38} H H H H H L_{A1278} CD_{3} H R^{G95} H H H
L_{A39} R^{G39} H H H H H L_{A1279} CD_{3} H R^{G96} H H H
L_{A40} R^{G40} H H H H H L_{A1280} CD_{3} H R^{G97} H H H
L_{A41} R^{G41} H H H H H L_{A1281} CD_{3} H R^{G98} H H H
L_{A42} R^{G42} H H H H H L_{A1282} CD_{3} H R^{G99} H H H
L_{A43} R^{G43} H H H H H L_{A1283} CD_{3} H R^{G100} H H H
L_{A44} R^{G44} H H H H H L_{A1284} CD_{3} H R^{G101} H H H
L_{A45} R^{G45} H H H H H L_{A1285} CD_{3} H R^{G102} H H H
L_{A46} R^{G46} H H H H H L_{A1286} CD_{3} H R^{G103} H H H
L_{A47} R^{G47} H H H H H L_{A1287} CD_{3} H R^{G104} H H H
L_{A48} R^{G48} H H H H H L_{A1288} CD_{3} H R^{G105} H H H
L_{A49} R^{G49} H H H H H L_{A1289} CD_{3} H R^{G106} H H H
L_{A50} R^{G50} H H H H H L_{A1290} CD_{3} H R^{G107} H H H
L_{A51} R^{G51} H H H H H L_{A1291} CD_{3} H R^{G108} H H H
L_{A52} R^{G52} H H H H H L_{A1292} CD_{3} H R^{G109} H H H
Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6} Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6}
L_{A53} R^{G53} H H H H H L_{A1293} CD_{3} H R^{G110} H H H
L_{A54} R^{G54} H H H H H L_{A1294} CD_{3} H R^{G111} H H H
L_{A55} R^{G55} H H H H H L_{A1295} CD_{3} H R^{G112} H H H
L_{A56} R^{G56} H H H H H L_{A1296} CD_{3} H R^{G113} H H H
L_{A57} R^{G57} H H H H H L_{A1297} CD_{3} H R^{G114} H H H
L_{A58} R^{G58} H H H H H L_{A1298} CD_{3} H R^{G115} H H H
L_{A59} R^{G59} H H H H H L_{A1299} CD_{3} H R^{G116} H H H
L_{A60} R^{G60} H H H H H L_{A1300} CD_{3} H R^{G117} H H H
L_{A61} R^{G61} H H H H H L_{A1301} CD_{3} H R^{G118} H H H
L_{A62} R^{G62} H H H H H L_{A1302} CD_{3} H R^{G119} H H H
L_{A63} R^{G63} H H H H H L_{A1303} CD_{3} H R^{G120} H H H
L_{A64} R^{G64} H H H H H L_{A1304} CD_{3} H R^{G121} H H H
L_{A65} R^{G65} H H H H H L_{A1305} CD_{3} H R^{G122} H H H
L_{A66} R^{G66} H H H H H L_{A1306} CD_{3} H R^{G123} H H H
L_{A67} R^{G67} H H H H H L_{A1307} CD_{3} H R^{G124} H H H
L_{A68} R^{G68} H H H H H L_{A1308} CD_{3} H R^{G125} H H H
L_{A69} R^{G69} H H H H H L_{A1309} CD_{3} H R^{G126} H H H
L_{A70} R^{G70} H H H H H L_{A1310} CD_{3} H R^{G127} H H H
L_{A71} R^{G71} H H H H H L_{A1311} CD_{3} H R^{G128} H H H
L_{A72} R^{G72} H H H H H L_{A1312} CD_{3} H R^{G129} H H H
L_{A73} R^{G73} H H H H H L_{A1313} CD_{3} H R^{G130} H H H
L_{A74} R^{G74} H H H H H L_{A1314} CD_{3} H R^{G131} H H H
L_{A75} R^{G75} H H H H H L_{A1315} CD_{3} H R^{G132} H H H
L_{A76} R^{G76} H H H H H L_{A1316} CD_{3} H R^{G133} H H H
Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6} Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6}
L_{A77} R^{G77} H H H H H L_{A1317} CD_{3} H R^{G134} H H H
L_{A78} R^{G78} H H H H H L_{A1318} CD_{3} H R^{G135} H H H
L_{A79} R^{G79} H H H H H L_{A1319} CD_{3} H R^{G136} H H H
L_{A80} R^{G80} H H H H H L_{A1320} CD_{3} H R^{G137} H H H
L_{A81} R^{G81} H H H H H L_{A1321} CD_{3} H R^{G138} H H H
L_{A82} R^{G82} H H H H H L_{A1322} CD_{3} H R^{G139} H H H
L_{A83} R^{G83} H H H H H L_{A1323} CD_{3} H R^{G140} H H H
L_{A84} R^{G84} H H H H H L_{A1324} CD_{3} H R^{G141} H H H
L_{A85} R^{G85} H H H H H L_{A13 25} CD_{3} H R^{G142} H H H
L_{A86} R^{G86} H H H H H L_{A1326} CD_{3} H R^{G143} H H H
L_{A87} R^{G87} H H H H H L_{A1327} CD_{3} H R^{G144} H H H
L_{A88} R^{G88} H H H H H L_{A1328} CD_{3} H R^{G145} H H H
L_{A89} R^{G89} H H H H H L_{A1329} CD_{3} H R^{G146} H H H
L_{A90} R^{G90} H H H H H L_{A1330} CD_{3} H R^{G147} H H H
L_{A91} R^{G91} H H H H H L_{A1331} CD_{3} H R^{G148} H H H
L_{A92} R^{G92} H H H H H L_{A1332} CD_{3} H R^{G149} H H H
L_{A93} R^{G93} H H H H H L_{A1333} CD_{3} H R^{G150} H H H
L_{A94} R^{G94} H H H H H L_{A1334} CD_{3} H R^{G151} H H H
L_{A95} R^{G95} H H H H H L_{A1335} CD_{3} H R^{G152} H H H
L_{A96} R^{G96} H H H H H L_{A1336} CD_{3} H R^{G153} H H H
L_{A97} R^{G97} H H H H H L_{A1337} CD_{3} H R^{G154} H H H
L_{A98} R^{G98} H H H H H L_{A1338} CD_{3} H R^{G155} H H H
L_{A99} R^{G99} H H H H H L_{A1339} CD_{3} H R^{G156} H H H
L_{A100} R^{G100} H H H H H L_{A1340} CD_{3} H R^{G157} H H H
Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6} Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6}
L_{A101} R^{G101} H H H H H L_{A1341} CD_{3} H R^{G158} H H H
L_{A102} R^{G102} H H H H H L_{A1342} CD_{3} H R^{G159} H H H
L_{A103} R^{G103} H H H H H L_{A1343} CD_{3} H R^{G160} H H H
L_{A104} R^{G104} H H H H H L_{A1344} CD_{3} H R^{G161} H H H
L_{A105} R^{G105} H H H H H L_{A1345} CD_{3} H R^{G162} H H H
L_{A106} R^{G106} H H H H H L_{A1346} CD_{3} H R^{G163} H H H
L_{A107} R^{G107} H H H H H L_{A1347} CD_{3} H R^{G164} H H H
L_{A108} R^{G108} H H H H H L_{A1348} CD_{3} H R^{G165} H H H
L_{A109} R^{G109} H H H H H L_{A1349} CD_{3} H R^{G166} H H H
L_{A110} R^{G110} H H H H H L_{A1350} CD_{3} H R^{G167} H H H
L_{A111} R^{G111} H H H H H L_{A1351} CD_{3} H R^{G168} H H H
L_{A112} R^{G112} H H H H H L_{A1352} CD_{3} H R^{G169} H H H
L_{A113} R^{G113} H H H H H L_{A1353} H CD_{3} R^{G1} H H H
L_{A114} R^{G114} H H H H H L_{A1354} H CD_{3} R^{G2} H H H
L_{A115} R^{G115} H H H H H L_{A1355} H CD_{3} R^{G3} H H H
L_{A116} R^{G116} H H H H H L_{A1356} H CD_{3} R^{G4} H H H
L_{A117} R^{G117} H H H H H L_{A1357} H CD_{3} R^{G5} H H H
L_{A118} R^{G118} H H H H H L_{A1358} H CD_{3} R^{G6} H H H
L_{A119} R^{G119} H H H H H L_{A1359} H CD_{3} R^{G7} H H H
L_{A120} R^{G120} H H H H H L_{A1360} H CD_{3} R^{G8} H H H
L_{A121} R^{G121} H H H H H L_{A1361} H CD_{3} R^{G9} H H H
L_{A122} R^{G122} H H H H H L_{A1362} H CD_{3} R^{G10} H H H
L_{A123} R^{G123} H H H H H L_{A1363} H CD_{3} R^{G11} H H H
L_{A124} R^{G124} H H H H H L_{A1364} H CD_{3} R^{G12} H H H
Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6} Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6}
L_{A125} R^{G125} H H H H H L_{A1365} H CD_{3} R^{G13} H H H
L_{A126} R^{G126} H H H H H L_{A1366} H CD_{3} R^{G14} H H H
L_{A127} R^{G127} H H H H H L_{A1367} H CD_{3} R^{G15} H H H
L_{A128} R^{G128} H H H H H L_{A1368} H CD_{3} R^{G16} H H H
L_{A129} R^{G129} H H H H H L_{A1369} H CD_{3} R^{G17} H H H
L_{A130} R^{G130} H H H H H L_{A1370} H CD_{3} R^{G18} H H H
L_{A131} R^{G131} H H H H H L_{A1371} H CD_{3} R^{G19} H H H
L_{A132} R^{G132} H H H H H L_{A1372} H CD_{3} R^{G20} H H H
L_{A133} R^{G133} H H H H H L_{A1373} H CD_{3} R^{G21} H H H
L_{A134} R^{G134} H H H H H L_{A1374} H CD_{3} R^{G22} H H H
L_{A135} R^{G135} H H H H H L_{A1375} H CD_{3} R^{G23} H H H
L_{A136} R^{G136} H H H H H L_{A1376} H CD_{3} R^{G24} H H H
L_{A137} R^{G137} H H H H H L_{A1377} H CD_{3} R^{G25} H H H
L_{A138} R^{G138} H H H H H L_{A1378} H CD_{3} R^{G26} H H H
L_{A139} R^{G139} H H H H H L_{A1379} H CD_{3} R^{G27} H H H
L_{A140} R^{G140} H H H H H L_{A1380} H CD_{3} R^{G28} H H H
L_{A141} R^{G141} H H H H H L_{A1381} H CD_{3} R^{G29} H H H
L_{A142} R^{G142} H H H H H L_{A1382} H CD_{3} R^{G30} H H H
L_{A143} R^{G143} H H H H H L_{A1383} H CD_{3} R^{G31} H H H
L_{A144} R^{G144} H H H H H L_{A1384} H CD_{3} R^{G32} H H H
L_{A145} R^{G145} H H H H H L_{A1385} H CD_{3} R^{G33} H H H
L_{A146} R^{G146} H H H H H L_{A1386} H CD_{3} R^{G34} H H H
L_{A147} R^{G147} H H H H H L_{A1387} H CD_{3} R^{G35} H H H
L_{A148} R^{G148} H H H H H L_{A1388} H CD_{3} R^{G36} H H H
Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6} Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6}
L_{A149} R^{G149} H H H H H L_{A1389} H CD_{3} R^{G37} H H H
L_{A150} R^{G150} H H H H H L_{A1390} H CD_{3} R^{G38} H H H
L_{A151} R^{G151} H H H H H L_{A1391} H CD_{3} R^{G39} H H H
L_{A152} R^{G152} H H H H H L_{A1392} H CD_{3} R^{G40} H H H
L_{A153} R^{G153} H H H H H L_{A1393} H CD_{3} R^{G41} H H H
L_{A154} R^{G154} H H H H H L_{A1394} H CD_{3} R^{G42} H H H
L_{A155} R^{G155} H H H H H L_{A1395} H CD_{3} R^{G43} H H H
L_{A156} R^{G156} H H H H H L_{A1396} H CD_{3} R^{G44} H H H
L_{A157} R^{G157} H H H H H L_{A1397} H CD_{3} R^{G45} H H H
L_{A158} R^{G158} H H H H H L_{A1398} H CD_{3} R^{G46} H H H
L_{A159} R^{G159} H H H H H L_{A1399} H CD_{3} R^{G47} H H H
L_{A160} R^{G160} H H H H H L_{A1400} H CD_{3} R^{G48} H H H
L_{A161} R^{G161} H H H H H L_{A1401} H CD_{3} R^{G49} H H H
L_{A162} R^{G162} H H H H H L_{A1402} H CD_{3} R^{G50} H H H
L_{A163} R^{G163} H H H H H L_{A1403} H CD_{3} R^{G51} H H H
L_{A164} R^{G164} H H H H H L_{A1404} H CD_{3} R^{G52} H H H
L_{A165} R^{G165} H H H H H L_{A1405} H CD_{3} R^{G53} H H H
L_{A166} R^{G166} H H H H H L_{A1406} H CD_{3} R^{G54} H H H
L_{A167} R^{G167} H H H H H L_{A1407} H CD_{3} R^{G55} H H H
L_{A168} R^{G168} H H H H H L_{A1408} H CD_{3} R^{G56} H H H
L_{A169} R^{G169} H H H H H L_{A1409} H CD_{3} R^{G57} H H H
L_{A170} R^{G1} H CD_{3} H H H L_{A1410} H CD_{3} R^{G58} H H H
L_{A171} R^{G2} H CD_{3} H H H L_{A1411} H CD_{3} R^{G59} H H H
L_{A172} R^{G3} H CD_{3} H H H L_{A1412} H CD_{3} R^{G60} H H H
Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6} Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6}
L_{A173} R^{G4} H CD_{3} H H H L_{A1413} H CD_{3} R^{G61} H H H
L_{A174} R^{G5} H CD_{3} H H H L_{A1414} H CD_{3} R^{G62} H H H
L_{A175} R^{G6} H CD_{3} H H H L_{A1415} H CD_{3} R^{G63} H H H
L_{A176} R^{G7} H CD_{3} H H H L_{A1416} H CD_{3} R^{G64} H H H
L_{A177} R^{G8} H CD_{3} H H H L_{A1417} H CD_{3} R^{G65} H H H
L_{A178} R^{G9} H CD_{3} H H H L_{A1418} H CD_{3} R^{G66} H H H
L_{A179} R^{G10} H CD_{3} H H H L_{A1419} H CD_{3} R^{G67} H H H
L_{A180} R^{G11} H CD_{3} H H H L_{A1420} H CD_{3} R^{G68} H H H
L_{A181} R^{G12} H CD_{3} H H H L_{A1421} H CD_{3} R^{G69} H H H
L_{A182} R^{G13} H CD_{3} H H H L_{A1422} H CD_{3} R^{G70} H H H
L_{A183} R^{G14} H CD_{3} H H H L_{A1423} H CD_{3} R^{G71} H H H
L_{A184} R^{G15} H CD_{3} H H H L_{A1424} H CD_{3} R^{G72} H H H
L_{A185} R^{G16} H CD_{3} H H H L_{A1425} H CD_{3} R^{G73} H H H
L_{A186} R^{G17} H CD_{3} H H H L_{A1426} H CD_{3} R^{G74} H H H
L_{A187} R^{G18} H CD_{3} H H H L_{A1427} H CD_{3} R^{G75} H H H
L_{A188} R^{G19} H CD_{3} H H H L_{A1428} H CD_{3} R^{G76} H H H
L_{A189} R^{G20} H CD_{3} H H H L_{A1429} H CD_{3} R^{G77} H H H
L_{A190} R^{G21} H CD_{3} H H H L_{A1430} H CD_{3} R^{G78} H H H
L_{A191} R^{G22} H CD_{3} H H H L_{A1431} H CD_{3} R^{G79} H H H
L_{A192} R^{G23} H CD_{3} H H H L_{A1432} H CD_{3} R^{G80} H H H
L_{A193} R^{G24} H CD_{3} H H H L_{A1433} H CD_{3} R^{G81} H H H
L_{A194} R^{G25} H CD_{3} H H H L_{A1434} H CD_{3} R^{G82} H H H
L_{A195} R^{G26} H CD_{3} H H H L_{A1435} H CD_{3} R^{G83} H H H
L_{A196} R^{G27} H CD_{3} H H H L_{A1436} H CD_{3} R^{G84} H H H
Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6} Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6}
L_{A197} R^{G28} H CD_{3} H H H L_{A1437} H CD_{3} R^{G85} H H H
L_{A198} R^{G29} H CD_{3} H H H L_{A1438} H CD_{3} R^{G86} H H H
L_{A199} R^{G30} H CD_{3} H H H L_{A1439} H CD_{3} R^{G87} H H H
L_{A200} R^{G31} H CD_{3} H H H L_{A1440} H CD_{3} R^{G88} H H H
L_{A201} R^{G32} H CD_{3} H H H L_{A1441} H CD_{3} R^{G89} H H H
L_{A202} R^{G33} H CD_{3} H H H L_{A1442} H CD_{3} R^{G90} H H H
L_{A203} R^{G34} H CD_{3} H H H L_{A1443} H CD_{3} R^{G91} H H H
L_{A204} R^{G35} H CD_{3} H H H L_{A1444} H CD_{3} R^{G92} H H H
L_{A205} R^{G36} H CD_{3} H H H L_{A1445} H CD_{3} R^{G93} H H H
L_{A206} R^{G37} H CD_{3} H H H L_{A1446} H CD_{3} R^{G94} H H H
L_{A207} R^{G38} H CD_{3} H H H L_{A1447} H CD_{3} R^{G95} H H H
L_{A208} R^{G39} H CD_{3} H H H L_{A1448} H CD_{3} R^{G96} H H H
L_{A209} R^{G40} H CD_{3} H H H L_{A1449} H CD_{3} R^{G97} H H H
L_{A210} R^{G41} H CD_{3} H H H L_{A1450} H CD_{3} R^{G98} H H H
L_{A211} R^{G42} H CD_{3} H H H L_{A1451} H CD_{3} R^{G99} H H H
L_{A212} R^{G43} H CD_{3} H H H L_{A1452} H CD_{3} R^{G100} H H H
L_{A213} R^{G44} H CD_{3} H H H L_{A1453} H CD_{3} R^{G101} H H H
L_{A214} R^{G45} H CD_{3} H H H L_{A1454} H CD_{3} R^{G102} H H H
L_{A215} R^{G46} H CD_{3} H H H L_{A1455} H CD_{3} R^{G103} H H H
L_{A216} R^{G47} H CD_{3} H H H L_{A1456} H CD_{3} R^{G104} H H H
L_{A217} R^{G48} H CD_{3} H H H L_{A1457} H CD_{3} R^{G105} H H H
L_{A218} R^{G49} H CD_{3} H H H L_{A1458} H CD_{3} R^{G106} H H H
L_{A219} R^{G50} H CD_{3} H H H L_{A1459} H CD_{3} R^{G107} H H H
L_{A220} R^{G51} H CD_{3} H H H L_{A1460} H CD_{3} R^{G108} H H H
Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6} Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6}
L_{A221} R^{G52} H CD_{3} H H H L_{A1461} H CD_{3} R^{G109} H H H
L_{A222} R^{G53} H CD_{3} H H H L_{A1462} H CD_{3} R^{G110} H H H
L_{A223} R^{G54} H CD_{3} H H H L_{A1463} H CD_{3} R^{G111} H H H
L_{A224} R^{G55} H CD_{3} H H H L_{A1464} H CD_{3} R^{G112} H H H
L_{A225} R^{G56} H CD_{3} H H H L_{A1465} H CD_{3} R^{G113} H H H
L_{A226} R^{G57} H CD_{3} H H H L_{A1466} H CD_{3} R^{G114} H H H
L_{A227} R^{G58} H CD_{3} H H H L_{A1467} H CD_{3} R^{G115} H H H
L_{A228} R^{G59} H CD_{3} H H H L_{A1468} H CD_{3} R^{G116} H H H
L_{A229} R^{G60} H CD_{3} H H H L_{A1469} H CD_{3} R^{G117} H H H
L_{A230} R^{G61} H CD_{3} H H H L_{A1470} H CD_{3} R^{G118} H H H
L_{A231} R^{G62} H CD_{3} H H H L_{A1471} H CD_{3} R^{G119} H H H
L_{A232} R^{G63} H CD_{3} H H H L_{A1472} H CD_{3} R^{G120} H H H
L_{A233} R^{G64} H CD_{3} H H H L_{A1473} H CD_{3} R^{G121} H H H
L_{A234} R^{G65} H CD_{3} H H H L_{A1474} H CD_{3} R^{G122} H H H
L_{A235} R^{G66} H CD_{3} H H H L_{A1475} H CD_{3} R^{G123} H H H
L_{A236} R^{G67} H CD_{3} H H H L_{A1476} H CD_{3} R^{G124} H H H
L_{A237} R^{G68} H CD_{3} H H H L_{A1477} H CD_{3} R^{G125} H H H
L_{A238} R^{G69} H CD_{3} H H H L_{A1478} H CD_{3} R^{G126} H H H
L_{A239} R^{G70} H CD_{3} H H H L_{A1479} H CD_{3} R^{G127} H H H
L_{A240} R^{G71} H CD_{3} H H H L_{A1480} H CD_{3} R^{G128} H H H
L_{A241} R^{G72} H CD_{3} H H H L_{A1481} H CD_{3} R^{G129} H H H
L_{A242} R^{G73} H CD_{3} H H H L_{A1482} H CD_{3} R^{G130} H H H
L_{A243} R^{G74} H CD_{3} H H H L_{A1483} H CD_{3} R^{G131} H H H
L_{A244} R^{G75} H CD_{3} H H H L_{A1484} H CD_{3} R^{G132} H H H
Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6} Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6}
L_{A245} R^{G76} H CD_{3} H H H L_{A1485} H CD_{3} R^{G133} H H H
L_{A246} R^{G77} H CD_{3} H H H L_{A1486} H CD_{3} R^{G134} H H H
L_{A247} R^{G78} H CD_{3} H H H L_{A1487} H CD_{3} R^{G135} H H H
L_{A248} R^{G79} H CD_{3} H H H L_{A1488} H CD_{3} R^{G136} H H H
L_{A249} R^{G80} H CD_{3} H H H L_{A1489} H CD_{3} R^{G137} H H H
L_{A250} R^{G81} H CD_{3} H H H L_{A1490} H CD_{3} R^{G138} H H H
L_{A251} R^{G82} H CD_{3} H H H L_{A1491} H CD_{3} R^{G139} H H H
L_{A252} R^{G83} H CD_{3} H H H L_{A1492} H CD_{3} R^{G140} H H H
L_{A253} R^{G84} H CD_{3} H H H L_{A1493} H CD_{3} R^{G141} H H H
L_{A254} R^{G85} H CD_{3} H H H L_{A1494} H CD_{3} R^{G142} H H H
L_{A255} R^{G86} H CD_{3} H H H L_{A1495} H CD_{3} R^{G143} H H H
L_{A256} R^{G87} H CD_{3} H H H L_{A1496} H CD_{3} R^{G144} H H H
L_{A257} R^{G88} H CD_{3} H H H L_{A1497} H CD_{3} R^{G145} H H H
L_{A258} R^{G89} H CD_{3} H H H L_{A1498} H CD_{3} R^{G146} H H H
L_{A259} R^{G90} H CD_{3} H H H L_{A1499} H CD_{3} R^{G147} H H H
L_{A260} R^{G91} H CD_{3} H H H L_{A1500} H CD_{3} R^{G148} H H H
L_{A261} R^{G92} H CD_{3} H H H L_{A1501} H CD_{3} R^{G149} H H H
L_{A262} R^{G93} H CD_{3} H H H L_{A1502} H CD_{3} R^{G150} H H H
L_{A263} R^{G94} H CD_{3} H H H L_{A1503} H CD_{3} R^{G151} H H H
L_{A264} R^{G95} H CD_{3} H H H L_{A1504} H CD_{3} R^{G152} H H H
L_{A265} R^{G96} H CD_{3} H H H L_{A1505} H CD_{3} R^{G153} H H H
L_{A266} R^{G97} H CD_{3} H H H L_{A1506} H CD_{3} R^{G154} H H H
L_{A267} R^{G98} H CD_{3} H H H L_{A1507} H CD_{3} R^{G155} H H H
L_{A268} R^{G99} H CD_{3} H H H L_{A1508} H CD_{3} R^{G156} H H H
Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6} Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6}
L_{A269} R^{G100} H CD_{3} H H H L_{A1509} H CD_{3} R^{G157} H H H
L_{A270} R^{G101} H CD_{3} H H H L_{A1510} H CD_{3} R^{G158} H H H
L_{A271} R^{G102} H CD_{3} H H H L_{A1511} H CD_{3} R^{G159} H H H
L_{A272} R^{G103} H CD_{3} H H H L_{A1512} H CD_{3} R^{G160} H H H
L_{A273} R^{G104} H CD_{3} H H H L_{A1513} H CD_{3} R^{G161} H H H
L_{A274} R^{G105} H CD_{3} H H H L_{A1514} H CD_{3} R^{G162} H H H
L_{A275} R^{G106} H CD_{3} H H H L_{A1515} H CD_{3} R^{G163} H H H
L_{A276} R^{G107} H CD_{3} H H H L_{A1516} H CD_{3} R^{G164} H H H
L_{A277} R^{G108} H CD_{3} H H H L_{A1517} H CD_{3} R^{G165} H H H
L_{A278} R^{G109} H CD_{3} H H H L_{A1518} H CD_{3} R^{G166} H H H
L_{A279} R^{G110} H CD_{3} H H H L_{A1519} H CD_{3} R^{G167} H H H
L_{A280} R^{G111} H CD_{3} H H H L_{A1520} H CD_{3} R^{G168} H H H
L_{A281} R^{G112} H CD_{3} H H H L_{A1521} H CD_{3} R^{G169} H H H
L_{A282} R^{G113} H CD_{3} H H H L_{A1522} R^{G1} CD_{3} CD_{3} H H H
L_{A283} R^{G114} H CD_{3} H H H L_{A1523} R^{G2} CD_{3} CD_{3} H H H
L_{A284} R^{G115} H CD_{3} H H H L_{A1524} R^{G3} CD_{3} CD_{3} H H H
L_{A285} R^{G116} H CD_{3} H H H L_{A1525} R^{G4} CD_{3} CD_{3} H H H
L_{A286} R^{G117} H CD_{3} H H H L_{A1526} R^{G5} CD_{3} CD_{3} H H H
L_{A287} R^{G118} H CD_{3} H H H L_{A1527} R^{G6} CD_{3} CD_{3} H H H
L_{A288} R^{G119} H CD_{3} H H H L_{A1528} R^{G7} CD_{3} CD_{3} H H H
L_{A289} R^{G120} H CD_{3} H H H L_{A1529} R^{G8} CD_{3} CD_{3} H H H
L_{A290} R^{G121} H CD_{3} H H H L_{A1530} R^{G9} CD_{3} CD_{3} H H H
L_{A291} R^{G122} H CD_{3} H H H L_{A1531} R^{G10} CD_{3} CD_{3} H H H
L_{A292} R^{G123} H CD_{3} H H H L_{A1532} R^{G11} CD_{3} CD_{3} H H H
Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6} Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6}
L_{A293} R^{G124} H CD_{3} H H H L_{A1533} R^{G12} CD_{3} CD_{3} H H H
L_{A294} R^{G125} H CD_{3} H H H L_{A1534} R^{G13} CD_{3} CD_{3} H H H
L_{A295} R^{G126} H CD_{3} H H H L_{A1535} R^{G14} CD_{3} CD_{3} H H H
L_{A296} R^{G127} H CD_{3} H H H L_{A1536} R^{G15} CD_{3} CD_{3} H H H
L_{A297} R^{G128} H CD_{3} H H H L_{A1537} R^{G16} CD_{3} CD_{3} H H H
L_{A298} R^{G129} H CD_{3} H H H L_{A1538} R^{G17} CD_{3} CD_{3} H H H
L_{A299} R^{G130} H CD_{3} H H H L_{A1539} R^{G18} CD_{3} CD_{3} H H H
L_{A300} R^{G131} H CD_{3} H H H L_{A1540} R^{G19} CD_{3} CD_{3} H H H
L_{A301} R^{G132} H CD_{3} H H H L_{A1541} CD_{3} R^{G1} H H H H
L_{A302} R^{G133} H CD_{3} H H H L_{A1542} CD_{3} R^{G2} H H H H
L_{A303} R^{G134} H CD_{3} H H H L_{A1543} CD_{3} R^{G3} H H H H
L_{A304} R^{G135} H CD_{3} H H H L_{A1544} CD_{3} R^{G4} H H H H
L_{A305} R^{G136} H CD_{3} H H H L_{A1545} CD_{3} R^{G5} H H H H
L_{A306} R^{G137} H CD_{3} H H H L_{A1546} CD_{3} R^{G6} H H H H
L_{A307} R^{G138} H CD_{3} H H H L_{A1547} CD_{3} R^{G7} H H H H
L_{A308} R^{G139} H CD_{3} H H H L_{A1548} CD_{3} R^{G8} H H H H
L_{A309} R^{G140} H CD_{3} H H H L_{A1549} CD_{3} R^{G9} H H H H
L_{A310} R^{G141} H CD_{3} H H H L_{A1550} CD_{3} R^{G10} H H H H
L_{A311} R^{G142} H CD_{3} H H H L_{A1551} CD_{3} R^{G11} H H H H
L_{A312} R^{G143} H CD_{3} H H H L_{A1552} CD_{3} R^{G12} H H H H
L_{A313} R^{G144} H CD_{3} H H H L_{A1553} CD_{3} R^{G13} H H H H
L_{A314} R^{G145} H CD_{3} H H H L_{A1554} CD_{3} R^{G14} H H H H
L_{A315} R^{G146} H CD_{3} H H H L_{A1555} CD_{3} R^{G15} H H H H
L_{A316} R^{G147} H CD_{3} H H H L_{A1556} CD_{3} R^{G16} H H H H
Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6} Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6}
L_{A317} R^{G148} H CD_{3} H H H L_{A1557} CD_{3} R^{G17} H H H H
L_{A318} R^{G149} H CD_{3} H H H L_{A1558} CD_{3} R^{G18} H H H H
L_{A319} R^{G150} H CD_{3} H H H L_{A1559} CD_{3} R^{G19} H H H H
L_{A320} R^{G151} H CD_{3} H H H L_{A1560} CD_{3} CD_{3} R^{G1} H H CD_{3}
L_{A321} R^{G152} H CD_{3} H H H L_{A1561} CD_{3} CD_{3} R^{G2} H H CD_{3}
L_{A322} R^{G153} H CD_{3} H H H L_{A1562} CD_{3} CD_{3} R^{G3} H H CD_{3}
L_{A323} R^{G154} H CD_{3} H H H L_{A1563} CD_{3} CD_{3} R^{G4} H H CD_{3}
L_{A324} R^{G155} H CD_{3} H H H L_{A1564} CD_{3} CD_{3} R^{G5} H H CD_{3}
L_{A325} R^{G156} H CD_{3} H H H L_{A1565} CD_{3} CD_{3} R^{G6} H H CD_{3}
L_{A326} R^{G157} H CD_{3} H H H L_{A1566} CD_{3} CD_{3} R^{G7} H H CD_{3}
L_{A327} R^{G158} H CD_{3} H H H L_{A1567} CD_{3} CD_{3} R^{G8} H H CD_{3}
L_{A328} R^{G159} H CD_{3} H H H L_{A1568} CD_{3} CD_{3} R^{G9} H H CD_{3}
L_{A329} R^{G160} H CD_{3} H H H L_{A1569} CD_{3} CD_{3} R^{G10} H H CD_{3}
L_{A330} R^{G161} H CD_{3} H H H L_{A1570} CD_{3} CD_{3} R^{G11} H H CD_{3}
L_{A331} R^{G162} H CD_{3} H H H L_{A1571} CD_{3} CD_{3} R^{G12} H H CD_{3}
L_{A332} R^{G163} H CD_{3} H H H L_{A1572} CD_{3} CD_{3} R^{G13} H H CD_{3}
L_{A333} R^{G164} H CD_{3} H H H L_{A1573} CD_{3} CD_{3} R^{G14} H H CD_{3}
L_{A334} R^{G165} H CD_{3} H H H L_{A1574} CD_{3} CD_{3} R^{G15} H H CD_{3}
L_{A335} R^{G166} H CD_{3} H H H L_{A1575} CD_{3} CD_{3} R^{G16} H H CD_{3}
L_{A336} R^{G167} H CD_{3} H H H L_{A1576} CD_{3} CD_{3} R^{G17} H H CD_{3}
L_{A337} R^{G168} H CD_{3} H H H L_{A1577} CD_{3} CD_{3} R^{G18} H H CD_{3}
L_{A338} R^{G169} H CD_{3} H H H L_{A1578} CD_{3} CD_{3} R^{G19} H H CD_{3}
L_{A339} R^{G1} CD_{3} CD_{3} H H CD_{3} L_{A1579} CD_{3} H R^{G1} H H CD_{3}
L_{A340} R^{G2} CD_{3} CD_{3} H H CD_{3} L_{A1580} CD_{3} H R^{G2} H H CD_{3}
Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6} Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6}
L_{A341} R^{G3} CD_{3} CD_{3} H H CD_{3} L_{A1581} CD_{3} H R^{G3} H H CD_{3}
L_{A342} R^{G4} CD_{3} CD_{3} H H CD_{3} L_{A1582} CD_{3} H R^{G4} H H CD_{3}
L_{A343} R^{G5} CD_{3} CD_{3} H H CD_{3} L_{A1583} CD_{3} H R^{G5} H H CD_{3}
L_{A344} R^{G6} CD_{3} CD_{3} H H CD_{3} L_{A1584} CD_{3} H R^{G6} H H CD_{3}
L_{A345} R^{G7} CD_{3} CD_{3} H H CD_{3} L_{A1585} CD_{3} H R^{G7} H H CD_{3}
L_{A346} R^{G8} CD_{3} CD_{3} H H CD_{3} L_{A1586} CD_{3} H R^{G8} H H CD_{3}
L_{A347} R^{G9} CD_{3} CD_{3} H H CD_{3} L_{A1587} CD_{3} H R^{G9} H H CD_{3}
L_{A348} R^{G10} CD_{3} CD_{3} H H CD_{3} L_{A1588} CD_{3} H R^{G10} H H CD_{3}
L_{A349} R^{G11} CD_{3} CD_{3} H H CD_{3} L_{A1589} CD_{3} H R^{G11} H H CD_{3}
L_{A350} R^{G12} CD_{3} CD_{3} H H CD_{3} L_{A1590} CD_{3} H R^{G12} H H CD_{3}
L_{A351} R^{G13} CD_{3} CD_{3} H H CD_{3} L_{A1591} CD_{3} H R^{G13} H H CD_{3}
L_{A352} R^{G14} CD_{3} CD_{3} H H CD_{3} L_{A1592} CD_{3} H R^{G14} H H CD_{3}
L_{A353} R^{G15} CD_{3} CD_{3} H H CD_{3} L_{A1593} CD_{3} H R^{G15} H H CD_{3}
L_{A354} R^{G16} CD_{3} CD_{3} H H CD_{3} L_{A1594} CD_{3} H R^{G16} H H CD_{3}
L_{A355} R^{G17} CD_{3} CD_{3} H H CD_{3} L_{A1595} CD_{3} H R^{G17} H H CD_{3}
L_{A356} R^{G18} CD_{3} CD_{3} H H CD_{3} L_{A1596} CD_{3} H R^{G18} H H CD_{3}
L_{A357} R^{G19} CD_{3} CD_{3} H H CD_{3} L_{A1597} CD_{3} H R^{G19} H H CD_{3}
L_{A358} R^{G20} CD_{3} CD_{3} H H CD_{3} L_{A1598} R^{G1} CD_{3} H H H H
L_{A359} R^{G21} CD_{3} CD_{3} H H CD_{3} L_{A1599} R^{G2} CD_{3} H H H H
L_{A360} R^{G22} CD_{3} CD_{3} H H CD_{3} L_{A1600} R^{G3} CD_{3} H H H H
L_{A361} R^{G23} CD_{3} CD_{3} H H CD_{3} L_{A1601} R^{G4} CD_{3} H H H H
L_{A362} R^{G24} CD_{3} CD_{3} H H CD_{3} L_{A1602} R^{G5} CD_{3} H H H H
L_{A363} R^{G25} CD_{3} CD_{3} H H CD_{3} L_{A1603} R^{G6} CD_{3} H H H H
L_{A364} R^{G26} CD_{3} CD_{3} H H CD_{3} L_{A1604} R^{G7} CD_{3} H H H H
Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6} Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6}
L_{A365} R^{G27} CD_{3} CD_{3} H H CD_{3} L_{A1605} R^{G8} CD_{3} H H H H
L_{A366} R^{G28} CD_{3} CD_{3} H H CD_{3} L_{A1606} R^{G9} CD_{3} H H H H
L_{A367} R^{G29} CD_{3} CD_{3} H H CD_{3} L_{A1607} R^{G10} CD_{3} H H H H
L_{A368} R^{G30} CD_{3} CD_{3} H H CD_{3} L_{A1608} R^{G11} CD_{3} H H H H
L_{A369} R^{G31} CD_{3} CD_{3} H H CD_{3} L_{A1609} R^{G12} CD_{3} H H H H
L_{A370} R^{G32} CD_{3} CD_{3} H H CD_{3} L_{A1610} R^{G13} CD_{3} H H H H
L_{A371} R^{G33} CD_{3} CD_{3} H H CD_{3} L_{A1611} R^{G14} CD_{3} H H H H
L_{A372} R^{G34} CD_{3} CD_{3} H H CD_{3} L_{A1612} R^{G15} CD_{3} H H H H
L_{A373} R^{G35} CD_{3} CD_{3} H H CD_{3} L_{A1613} R^{G16} CD_{3} H H H H
L_{A374} R^{G36} CD_{3} CD_{3} H H CD_{3} L_{A1614} R^{G17} CD_{3} H H H H
L_{A375} R^{G37} CD_{3} CD_{3} H H CD_{3} L_{A1615} R^{G18} CD_{3} H H H H
L_{A376} R^{G38} CD_{3} CD_{3} H H CD_{3} L_{A1616} R^{G19} CD_{3} H H H H
L_{A377} R^{G39} CD_{3} CD_{3} H H CD_{3} L_{A1617} H CD_{3} R^{G1} H H CD_{3}
L_{A378} R^{G40} CD_{3} CD_{3} H H CD_{3} L_{A1618} H CD_{3} R^{G2} H H CD_{3}
L_{A379} R^{G41} CD_{3} CD_{3} H H CD_{3} L_{A1619} H CD_{3} R^{G3} H H CD_{3}
L_{A380} R^{G42} CD_{3} CD_{3} H H CD_{3} L_{A1620} H CD_{3} R^{G4} H H CD_{3}
L_{A381} R^{G43} CD_{3} CD_{3} H H CD_{3} L_{A1621} H CD_{3} R^{G5} H H CD_{3}
L_{A382} R^{G44} CD_{3} CD_{3} H H CD_{3} L_{A1622} H CD_{3} R^{G6} H H CD_{3}
L_{A383} R^{G45} CD_{3} CD_{3} H H CD_{3} L_{A1623} H CD_{3} R^{G7} H H CD_{3}
L_{A384} R^{G46} CD_{3} CD_{3} H H CD_{3} L_{A1624} H CD_{3} R^{G8} H H CD_{3}
L_{A385} R^{G47} CD_{3} CD_{3} H H CD_{3} L_{A1625} H CD_{3} R^{G9} H H CD_{3}
L_{A386} R^{G48} CD_{3} CD_{3} H H CD_{3} L_{A1626} H CD_{3} R^{G10} H H CD_{3}
L_{A387} R^{G49} CD_{3} CD_{3} H H CD_{3} L_{A1627} H CD_{3} R^{G11} H H CD_{3}
L_{A388} R^{G50} CD_{3} CD_{3} H H CD_{3} L_{A1628} H CD_{3} R^{G12} H H CD_{3}
Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6} Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6}
L_{A389} R^{G51} CD_{3} CD_{3} H H CD_{3} L_{A1629} H CD_{3} R^{G13} H H CD_{3}
L_{A390} R^{G52} CD_{3} CD_{3} H H CD_{3} L_{A1630} H CD_{3} R^{G14} H H CD_{3}
L_{A391} R^{G53} CD_{3} CD_{3} H H CD_{3} L_{A1631} H CD_{3} R^{G15} H H CD_{3}
L_{A392} R^{G54} CD_{3} CD_{3} H H CD_{3} L_{A1632} H CD_{3} R^{G16} H H CD_{3}
L_{A393} R^{G55} CD_{3} CD_{3} H H CD_{3} L_{A1633} H CD_{3} R^{G17} H H CD_{3}
L_{A394} R^{G56} CD_{3} CD_{3} H H CD_{3} L_{A1634} H CD_{3} R^{G18} H H CD_{3}
L_{A395} R^{G57} CD_{3} CD_{3} H H CD_{3} L_{A1635} H CD_{3} R^{G19} H H CD_{3}
L_{A396} R^{G58} CD_{3} CD_{3} H H CD_{3} L_{A1636} H R^{G1} H H H H
L_{A397} R^{G59} CD_{3} CD_{3} H H CD_{3} L_{A1637} H R^{G2} H H H H
L_{A398} R^{G60} CD_{3} CD_{3} H H CD_{3} L_{A1638} H R^{G3} H H H H
L_{A399} R^{G61} CD_{3} CD_{3} H H CD_{3} L_{A1639} H R^{G4} H H H H
L_{A400} R^{G62} CD_{3} CD_{3} H H CD_{3} L_{A1640} H R^{G5} H H H H
L_{A401} R^{G63} CD_{3} CD_{3} H H CD_{3} L_{A1641} H R^{G6} H H H H
L_{A402} R^{G64} CD_{3} CD_{3} H H CD_{3} L_{A1642} H R^{G7} H H H H
L_{A403} R^{G65} CD_{3} CD_{3} H H CD_{3} L_{A1643} H R^{G8} H H H H
L_{A404} R^{G66} CD_{3} CD_{3} H H CD_{3} L_{A1644} H R^{G9} H H H H
L_{A405} R^{G67} CD_{3} CD_{3} H H CD_{3} L_{A1645} H R^{G10} H H H H
L_{A406} R^{G68} CD_{3} CD_{3} H H CD_{3} L_{A1646} H R^{G11} H H H H
L_{A407} R^{G69} CD_{3} CD_{3} H H CD_{3} L_{A1647} H R^{G12} H H H H
L_{A408} R^{G70} CD_{3} CD_{3} H H CD_{3} L_{A1648} H R^{G13} H H H H
L_{A409} R^{G71} CD_{3} CD_{3} H H CD_{3} L_{A1649} H R^{G14} H H H H
L_{A410} R^{G72} CD_{3} CD_{3} H H CD_{3} L_{A1650} H R^{G15} H H H H
L_{A411} R^{G73} CD_{3} CD_{3} H H CD_{3} L_{A1651} H R^{G16} H H H H
L_{A412} R^{G74} CD_{3} CD_{3} H H CD_{3} L_{A1652} H R^{G17} H H H H
Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6} Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6}
L_{A413} R^{G75} CD_{3} CD_{3} H H CD_{3} L_{A1653} H R^{G18} H H H H
L_{A414} R^{G76} CD_{3} CD_{3} H H CD_{3} L_{A1654} H R^{G19} H H H H
L_{A415} R^{G77} CD_{3} CD_{3} H H CD_{3} L_{A1655} H R^{G20} H H H H
L_{A416} R^{G78} CD_{3} CD_{3} H H CD_{3} L_{A1656} H R^{G21} H H H H
L_{A417} R^{G79} CD_{3} CD_{3} H H CD_{3} L_{A1657} H R^{G22} H H H H
L_{A418} R^{G80} CD_{3} CD_{3} H H CD_{3} L_{A1658} H R^{G23} H H H H
L_{A419} R^{G81} CD_{3} CD_{3} H H CD_{3} L_{A1659} H R^{G24} H H H H
L_{A420} R^{G82} CD_{3} CD_{3} H H CD_{3} L_{A1660} H R^{G25} H H H H
L_{A421} R^{G83} CD_{3} CD_{3} H H CD_{3} L_{A1661} H R^{G26} H H H H
L_{A422} R^{G84} CD_{3} CD_{3} H H CD_{3} L_{A1662} H R^{G27} H H H H
L_{A423} R^{G85} CD_{3} CD_{3} H H CD_{3} L_{A1663} H R^{G28} H H H H
L_{A424} R^{G86} CD_{3} CD_{3} H H CD_{3} L_{A1664} H R^{G29} H H H H
L_{A425} R^{G87} CD_{3} CD_{3} H H CD_{3} L_{A1665} H R^{G30} H H H H
L_{A426} R^{G88} CD_{3} CD_{3} H H CD_{3} L_{A1666} H R^{G31} H H H H
L_{A427} R^{G89} CD_{3} CD_{3} H H CD_{3} L_{A1667} H R^{G32} H H H H
L_{A428} R^{G90} CD_{3} CD_{3} H H CD_{3} L_{A1668} H R^{G33} H H H H
L_{A429} R^{G91} CD_{3} CD_{3} H H CD_{3} L_{A1669} H R^{G34} H H H H
L_{A430} R^{G92} CD_{3} CD_{3} H H CD_{3} L_{A1670} H R^{G35} H H H H
L_{A431} R^{G93} CD_{3} CD_{3} H H CD_{3} L_{A1671} H R^{G36} H H H H
L_{A432} R^{G94} CD_{3} CD_{3} H H CD_{3} L_{A1672} H R^{G37} H H H H
L_{A433} R^{G95} CD_{3} CD_{3} H H CD_{3} L_{A1673} H R^{G38} H H H H
L_{A434} R^{G96} CD_{3} CD_{3} H H CD_{3} L_{A1674} H R^{G39} H H H H
L_{A435} R^{G97} CD_{3} CD_{3} H H CD_{3} L_{A1675} H R^{G40} H H H H
L_{A436} R^{G98} CD_{3} CD_{3} H H CD_{3} L_{A1676} H R^{G41} H H H H
Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6} Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6}
L_{A437} R^{G99} CD_{3} CD_{3} H H CD_{3} L_{A1677} H R^{G42} H H H H
L_{A438} R^{G100} CD_{3} CD_{3} H H CD_{3} L_{A1678} H R^{G43} H H H H
L_{A439} R^{G101} CD_{3} CD_{3} H H CD_{3} L_{A1679} H R^{G44} H H H H
L_{A440} R^{G102} CD_{3} CD_{3} H H CD_{3} L_{A1680} H R^{G45} H H H H
L_{A441} R^{G103} CD_{3} CD_{3} H H CD_{3} L_{A1681} H R^{G46} H H H H
L_{A442} R^{G104} CD_{3} CD_{3} H H CD_{3} L_{A1682} H R^{G47} H H H H
L_{A443} R^{G105} CD_{3} CD_{3} H H CD_{3} L_{A1683} H R^{G48} H H H H
L_{A444} R^{G106} CD_{3} CD_{3} H H CD_{3} L_{A1684} H R^{G49} H H H H
L_{A445} R^{G107} CD_{3} CD_{3} H H CD_{3} L_{A1685} H R^{G50} H H H H
L_{A446} R^{G108} CD_{3} CD_{3} H H CD_{3} L_{A1686} H R^{G51} H H H H
L_{A447} R^{G109} CD_{3} CD_{3} H H CD_{3} L_{A1687} H R^{G52} H H H H
L_{A448} R^{G110} CD_{3} CD_{3} H H CD_{3} L_{A1688} H R^{G53} H H H H
L_{A449} R^{G111} CD_{3} CD_{3} H H CD_{3} L_{A1689} H R^{G54} H H H H
L_{A450} R^{G112} CD_{3} CD_{3} H H CD_{3} L_{A1690} H R^{G55} H H H H
L_{A451} R^{G113} CD_{3} CD_{3} H H CD_{3} L_{A1691} H R^{G56} H H H H
L_{A452} R^{G114} CD_{3} CD_{3} H H CD_{3} L_{A1692} H R^{G57} H H H H
L_{A453} R^{G115} CD_{3} CD_{3} H H CD_{3} L_{A1693} H R^{G58} H H H H
L_{A454} R^{G116} CD_{3} CD_{3} H H CD_{3} L_{A1694} H R^{G59} H H H H
L_{A455} R^{G117} CD_{3} CD_{3} H H CD_{3} L_{A1695} H R^{G60} H H H H
L_{A456} R^{G118} CD_{3} CD_{3} H H CD_{3} L_{A1696} H R^{G61} H H H H
L_{A457} R^{G119} CD_{3} CD_{3} H H CD_{3} L_{A1697} H R^{G62} H H H H
L_{A458} R^{G120} CD_{3} CD_{3} H H CD_{3} L_{A1698} H R^{G63} H H H H
L_{A459} R^{G121} CD_{3} CD_{3} H H CD_{3} L_{A1699} H R^{G64} H H H H
L_{A460} R^{G122} CD_{3} CD_{3} H H CD_{3} L_{A1700} H R^{G65} H H H H
Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6} Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6}
L_{A461} R^{G123} CD_{3} CD_{3} H H CD_{3} L_{A1701} H R^{G66} H H H H
L_{A462} R^{G124} CD_{3} CD_{3} H H CD_{3} L_{A1702} H R^{G67} H H H H
L_{A463} R^{G125} CD_{3} CD_{3} H H CD_{3} L_{A1703} H R^{G68} H H H H
L_{A464} R^{G126} CD_{3} CD_{3} H H CD_{3} L_{A1704} H R^{G69} H H H H
L_{A465} R^{G127} CD_{3} CD_{3} H H CD_{3} L_{A1705} H R^{G70} H H H H
L_{A466} R^{G128} CD_{3} CD_{3} H H CD_{3} L_{A1706} H R^{G71} H H H H
L_{A467} R^{G129} CD_{3} CD_{3} H H CD_{3} L_{A1707} H R^{G72} H H H H
L_{A468} R^{G130} CD_{3} CD_{3} H H CD_{3} L_{A1708} H R^{G73} H H H H
L_{A469} R^{G131} CD_{3} CD_{3} H H CD_{3} L_{A1709} H R^{G74} H H H H
L_{A470} R^{G132} CD_{3} CD_{3} H H CD_{3} L_{A1710} H R^{G75} H H H H
L_{A471} R^{G133} CD_{3} CD_{3} H H CD_{3} L_{A1711} H R^{G76} H H H H
L_{A472} R^{G134} CD_{3} CD_{3} H H CD_{3} L_{A1712} H R^{G77} H H H H
L_{A473} R^{G135} CD_{3} CD_{3} H H CD_{3} L_{A1713} H R^{G78} H H H H
L_{A474} R^{G136} CD_{3} CD_{3} H H CD_{3} L_{A1714} H R^{G79} H H H H
L_{A475} R^{G137} CD_{3} CD_{3} H H CD_{3} L_{A1715} H R^{G80} H H H H
L_{A476} R^{G138} CD_{3} CD_{3} H H CD_{3} L_{A1716} H R^{G81} H H H H
L_{A477} R^{G139} CD_{3} CD_{3} H H CD_{3} L_{A1717} H R^{G82} H H H H
L_{A478} R^{G140} CD_{3} CD_{3} H H CD_{3} L_{A1718} H R^{G83} H H H H
L_{A479} R^{G141} CD_{3} CD_{3} H H CD_{3} L_{A1719} H R^{G84} H H H H
L_{A480} R^{G142} CD_{3} CD_{3} H H CD_{3} L_{A1720} H R^{G85} H H H H
L_{A481} R^{G143} CD_{3} CD_{3} H H CD_{3} L_{A1721} H R^{G86} H H H H
L_{A482} R^{G144} CD_{3} CD_{3} H H CD_{3} L_{A1722} H R^{G87} H H H H
L_{A483} R^{G145} CD_{3} CD_{3} H H CD_{3} L_{A1723} H R^{G88} H H H H
L_{A484} R^{G146} CD_{3} CD_{3} H H CD_{3} L_{A1724} H R^{G89} H H H H
Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6} Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6}
L_{A485} R^{G147} CD_{3} CD_{3} H H CD_{3} L_{A1725} H R^{G90} H H H H
L_{A486} R^{G148} CD_{3} CD_{3} H H CD_{3} L_{A1726} H R^{G91} H H H H
L_{A487} R^{G149} CD_{3} CD_{3} H H CD_{3} L_{A1727} H R^{G92} H H H H
L_{A488} R^{G150} CD_{3} CD_{3} H H CD_{3} L_{A1728} H R^{G93} H H H H
L_{A489} R^{G151} CD_{3} CD_{3} H H CD_{3} L_{A1729} H R^{G94} H H H H
L_{A490} R^{G152} CD_{3} CD_{3} H H CD_{3} L_{A1730} H R^{G95} H H H H
L_{A491} R^{G153} CD_{3} CD_{3} H H CD_{3} L_{A1731} H R^{G96} H H H H
L_{A492} R^{G154} CD_{3} CD_{3} H H CD_{3} L_{A1732} H R^{G97} H H H H
L_{A493} R^{G155} CD_{3} CD_{3} H H CD_{3} L_{A1733} H R^{G98} H H H H
L_{A494} R^{G156} CD_{3} CD_{3} H H CD_{3} L_{A1734} H R^{G99} H H H H
L_{A495} R^{G157} CD_{3} CD_{3} H H CD_{3} L_{A1735} H R^{G100} H H H H
L_{A496} R^{G158} CD_{3} CD_{3} H H CD_{3} L_{A1736} H R^{G101} H H H H
L_{A497} R^{G159} CD_{3} CD_{3} H H CD_{3} L_{A1737} H R^{G102} H H H H
L_{A498} R^{G160} CD_{3} CD_{3} H H CD_{3} L_{A1738} H R^{G103} H H H H
L_{A499} R^{G161} CD_{3} CD_{3} H H CD_{3} L_{A1739} H R^{G104} H H H H
L_{A500} R^{G162} CD_{3} CD_{3} H H CD_{3} L_{A1740} H R^{G105} H H H H
L_{A501} R^{G163} CD_{3} CD_{3} H H CD_{3} L_{A1741} H R^{G106} H H H H
L_{A502} R^{G164} CD_{3} CD_{3} H H CD_{3} L_{A1742} H R^{G107} H H H H
L_{A503} R^{G165} CD_{3} CD_{3} H H CD_{3} L_{A1743} H R^{G108} H H H H
L_{A504} R^{G166} CD_{3} CD_{3} H H CD_{3} L_{A1744} H R^{G109} H H H H
L_{A505} R^{G167} CD_{3} CD_{3} H H CD_{3} L_{A1745} H R^{G110} H H H H
L_{A506} R^{G168} CD_{3} CD_{3} H H CD_{3} L_{A1746} H R^{G111} H H H H
L_{A507} R^{G169} CD_{3} CD_{3} H H CD_{3} L_{A1747} H R^{G112} H H H H
L_{A508} H R^{G1} CD_{3} H H H L_{A1748} H R^{G113} H H H H
Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6} Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6}
L_{A509} H R^{G2} CD_{3} H H H L_{A1749} H R^{G114} H H H H
L_{A510} H R^{G3} CD_{3} H H H L_{A1750} H R^{G115} H H H H
L_{A511} H R^{G4} CD_{3} H H H L_{A1751} H R^{G116} H H H H
L_{A512} H R^{G5} CD_{3} H H H L_{A1752} H R^{G117} H H H H
L_{A513} H R^{G6} CD_{3} H H H L_{A1753} H R^{G118} H H H H
L_{A514} H R^{G7} CD_{3} H H H L_{A1754} H R^{G119} H H H H
L_{A515} H R^{G8} CD_{3} H H H L_{A1755} H R^{G120} H H H H
L_{A516} H R^{G9} CD_{3} H H H L_{A1756} H R^{G121} H H H H
L_{A517} H R^{G10} CD_{3} H H H L_{A1757} H R^{G122} H H H H
L_{A518} H R^{G11} CD_{3} H H H L_{A1758} H R^{G123} H H H H
L_{A519} H R^{G12} CD_{3} H H H L_{A1759} H R^{G124} H H H H
L_{A520} H R^{G13} CD_{3} H H H L_{A1760} H R^{G125} H H H H
L_{A521} H R^{G14} CD_{3} H H H L_{A1761} H R^{G126} H H H H
L_{A522} H R^{G15} CD_{3} H H H L_{A1762} H R^{G127} H H H H
L_{A523} H R^{G16} CD_{3} H H H L_{A1763} H R^{G128} H H H H
L_{A524} H R^{G17} CD_{3} H H H L_{A1764} H R^{G129} H H H H
L_{A525} H R^{G18} CD_{3} H H H L_{A1765} H R^{G130} H H H H
L_{A526} H R^{G19} CD_{3} H H H L_{A1766} H R^{G131} H H H H
L_{A527} H R^{G20} CD_{3} H H H L_{A1767} H R^{G132} H H H H
L_{A528} H R^{G21} CD_{3} H H H L_{A1768} H R^{G133} H H H H
L_{A529} H R^{G22} CD_{3} H H H L_{A1769} H R^{G134} H H H H
L_{A530} H R^{G23} CD_{3} H H H L_{A1770} H R^{G135} H H H H
L_{A531} H R^{G24} CD_{3} H H H L_{A1771} H R^{G136} H H H H
L_{A532} H R^{G25} CD_{3} H H H L_{A1772} H R^{G137} H H H H
Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6} Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6}
L_{A533} H R^{G26} CD_{3} H H H L_{A1773} H R^{G138} H H H H
L_{A534} H R^{G27} CD_{3} H H H L_{A1774} H R^{G139} H H H H
L_{A535} H R^{G28} CD_{3} H H H L_{A1775} H R^{G140} H H H H
L_{A536} H R^{G29} CD_{3} H H H L_{A1776} H R^{G141} H H H H
L_{A537} H R^{G30} CD_{3} H H H L_{A1777} H R^{G142} H H H H
L_{A538} H R^{G31} CD_{3} H H H L_{A1778} H R^{G143} H H H H
L_{A539} H R^{G32} CD_{3} H H H L_{A1779} H R^{G144} H H H H
L_{A540} H R^{G33} CD_{3} H H H L_{A1780} H R^{G145} H H H H
L_{A541} H R^{G34} CD_{3} H H H L_{A1781} H R^{G146} H H H H
L_{A542} H R^{G35} CD_{3} H H H L_{A1782} H R^{G147} H H H H
L_{A543} H R^{G36} CD_{3} H H H L_{A1783} H R^{G148} H H H H
L_{A544} H R^{G37} CD_{3} H H H L_{A1784} H R^{G149} H H H H
L_{A545} H R^{G38} CD_{3} H H H L_{A1785} H R^{G150} H H H H
L_{A546} H R^{G39} CD_{3} H H H L_{A1786} H R^{G151} H H H H
L_{A547} H R^{G40} CD_{3} H H H L_{A1787} H R^{G152} H H H H
L_{A548} H R^{G41} CD_{3} H H H L_{A1788} H R^{G153} H H H H
L_{A549} H R^{G42} CD_{3} H H H L_{A1789} H R^{G154} H H H H
L_{A550} H R^{G43} CD_{3} H H H L_{A1790} H R^{G155} H H H H
L_{A551} H R^{G44} CD_{3} H H H L_{A1791} H R^{G156} H H H H
L_{A552} H R^{G45} CD_{3} H H H L_{A1792} H R^{G157} H H H H
L_{A553} H R^{G46} CD_{3} H H H L_{A1793} H R^{G158} H H H H
L_{A554} H R^{G47} CD_{3} H H H L_{A1794} H R^{G159} H H H H
L_{A555} H R^{G48} CD_{3} H H H L_{A1795} H R^{G160} H H H H
L_{A556} H R^{G49} CD_{3} H H H L_{A1796} H R^{G161} H H H H
Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6} Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6}
L_{A557} H R^{G50} CD_{3} H H H L_{A1797} H R^{G162} H H H H
L_{A558} H R^{G51} CD_{3} H H H L_{A1798} H R^{G163} H H H H
L_{A559} H R^{G52} CD_{3} H H H L_{A1799} H R^{G164} H H H H
L_{A560} H R^{G53} CD_{3} H H H L_{A1800} H R^{G165} H H H H
L_{A561} H R^{G54} CD_{3} H H H L_{A1801} H R^{G166} H H H H
L_{A562} H R^{G55} CD_{3} H H H L_{A1802} H R^{G167} H H H H
L_{A563} H R^{G56} CD_{3} H H H L_{A1803} H R^{G168} H H H H
L_{A564} H R^{G57} CD_{3} H H H L_{A1804} H R^{G169} H H H H
L_{A565} H R^{G58} CD_{3} H H H L_{A1805} H H R^{G1} H H H
L_{A566} H R^{G59} CD_{3} H H H L_{A1806} H H R^{G2} H H H
L_{A567} H R^{G60} CD_{3} H H H L_{A1807} H H R^{G3} H H H
L_{A568} H R^{G61} CD_{3} H H H L_{A1808} H H R^{G4} H H H
L_{A569} H R^{G62} CD_{3} H H H L_{A1809} H H R^{G5} H H H
L_{A570} H R^{G63} CD_{3} H H H L_{A1810} H H R^{G6} H H H
L_{A571} H R^{G64} CD_{3} H H H L_{A1811} H H R^{G7} H H H
L_{A572} H R^{G65} CD_{3} H H H L_{A1812} H H R^{G8} H H H
L_{A573} H R^{G66} CD_{3} H H H L_{A1813} H H R^{G9} H H H
L_{A574} H R^{G67} CD_{3} H H H L_{A1814} H H R^{G10} H H H
L_{A575} H R^{G68} CD_{3} H H H L_{A1815} H H R^{G11} H H H
L_{A576} H R^{G69} CD_{3} H H H L_{A1816} H H R^{G12} H H H
L_{A577} H R^{G70} CD_{3} H H H L_{A1817} H H R^{G13} H H H
L_{A578} H R^{G71} CD_{3} H H H L_{A1818} H H R^{G14} H H H
L_{A579} H R^{G72} CD_{3} H H H L_{A1819} H H R^{G15} H H H
L_{A580} H R^{G73} CD_{3} H H H L_{A1820} H H R^{G16} H H H
Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6} Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6}
L_{A581} H R^{G74} CD_{3} H H H L_{A1821} H H R^{G17} H H H
L_{A582} H R^{G75} CD_{3} H H H L_{A1822} H H R^{G18} H H H
L_{A583} H R^{G76} CD_{3} H H H L_{A1823} H H R^{G19} H H H
L_{A584} H R^{G77} CD_{3} H H H L_{A1824} H H R^{G20} H H H
L_{A585} H R^{G78} CD_{3} H H H L_{A1825} H H R^{G21} H H H
L_{A586} H R^{G79} CD_{3} H H H L_{A1826} H H R^{G22} H H H
L_{A587} H R^{G80} CD_{3} H H H L_{A1827} H H R^{G23} H H H
L_{A588} H R^{G81} CD_{3} H H H L_{A1828} H H R^{G24} H H H
L_{A589} H R^{G82} CD_{3} H H H L_{A1829} H H R^{G25} H H H
L_{A590} H R^{G83} CD_{3} H H H L_{A1830} H H R^{G26} H H H
L_{A591} H R^{G84} CD_{3} H H H L_{A1831} H H R^{G27} H H H
L_{A592} H R^{G85} CD_{3} H H H L_{A1832} H H R^{G28} H H H
L_{A593} H R^{G86} CD_{3} H H H L_{A1833} H H R^{G29} H H H
L_{A594} H R^{G87} CD_{3} H H H L_{A1834} H H R^{G30} H H H
L_{A595} H R^{G88} CD_{3} H H H L_{A1835} H H R^{G31} H H H
L_{A596} H R^{G89} CD_{3} H H H L_{A1836} H H R^{G32} H H H
L_{A597} H R^{G90} CD_{3} H H H L_{A1837} H H R^{G33} H H H
L_{A598} H R^{G91} CD_{3} H H H L_{A1838} H H R^{G34} H H H
L_{A599} H R^{G92} CD_{3} H H H L_{A1839} H H R^{G35} H H H
L_{A600} H R^{G93} CD_{3} H H H L_{A1840} H H R^{G36} H H H
L_{A601} H R^{G94} CD_{3} H H H L_{A1841} H H R^{G37} H H H
L_{A602} H R^{G95} CD_{3} H H H L_{A1842} H H R^{G38} H H H
L_{A603} H R^{G96} CD_{3} H H H L_{A1843} H H R^{G39} H H H
L_{A604} H R^{G97} CD_{3} H H H L_{A1844} H H R^{G40} H H H
Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6} Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6}
L_{A605} H R^{G98} CD_{3} H H H L_{A1845} H H R^{G41} H H H
L_{A606} H R^{G99} CD_{3} H H H L_{A1846} H H R^{G42} H H H
L_{A607} H R^{G100} CD_{3} H H H L_{A1847} H H R^{G43} H H H
L_{A608} H R^{G101} CD_{3} H H H L_{A1848} H H R^{G44} H H H
L_{A609} H R^{G102} CD_{3} H H H L_{A1849} H H R^{G45} H H H
L_{A610} H R^{G103} CD_{3} H H H L_{A1850} H H R^{G46} H H H
L_{A611} H R^{G104} CD_{3} H H H L_{A1851} H H R^{G47} H H H
L_{A612} H R^{G105} CD_{3} H H H L_{A1852} H H R^{G48} H H H
L_{A613} H R^{G106} CD_{3} H H H L_{A1853} H H R^{G49} H H H
L_{A614} H R^{G107} CD_{3} H H H L_{A1854} H H R^{G50} H H H
L_{A615} H R^{G108} CD_{3} H H H L_{A1855} H H R^{G51} H H H
L_{A616} H R^{G109} CD_{3} H H H L_{A1856} H H R^{G52} H H H
L_{A617} H R^{G110} CD_{3} H H H L_{A1857} H H R^{G53} H H H
L_{A618} H R^{G111} CD_{3} H H H L_{A1858} H H R^{G54} H H H
L_{A619} H R^{G112} CD_{3} H H H L_{A1859} H H R^{G55} H H H
L_{A620} H R^{G113} CD_{3} H H H L_{A1860} H H R^{G56} H H H
L_{A621} H R^{G114} CD_{3} H H H L_{A1861} H H R^{G57} H H H
L_{A622} H R^{G115} CD_{3} H H H L_{A1862} H H R^{G58} H H H
L_{A623} H R^{G116} CD_{3} H H H L_{A1863} H H R^{G59} H H H
L_{A624} H R^{G117} CD_{3} H H H L_{A1864} H H R^{G60} H H H
L_{A625} H R^{G118} CD_{3} H H H L_{A1865} H H R^{G61} H H H
L_{A626} H R^{G119} CD_{3} H H H L_{A1866} H H R^{G62} H H H
L_{A627} H R^{G120} CD_{3} H H H L_{A1867} H H R^{G63} H H H
L_{A628} H R^{G121} CD_{3} H H H L_{A1868} H H R^{G64} H H H
Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6} Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6}
L_{A629} H R^{G122} CD_{3} H H H L_{A1869} H H R^{G65} H H H
L_{A630} H R^{G123} CD_{3} H H H L_{A1870} H H R^{G66} H H H
L_{A631} H R^{G124} CD_{3} H H H L_{A1871} H H R^{G67} H H H
L_{A632} H R^{G125} CD_{3} H H H L_{A1872} H H R^{G68} H H H
L_{A633} H R^{G126} CD_{3} H H H L_{A1873} H H R^{G69} H H H
L_{A634} H R^{G127} CD_{3} H H H L_{A1874} H H R^{G70} H H H
L_{A635} H R^{G128} CD_{3} H H H L_{A1875} H H R^{G71} H H H
L_{A636} H R^{G129} CD_{3} H H H L_{A1876} H H R^{G72} H H H
L_{A637} H R^{G130} CD_{3} H H H L_{A1877} H H R^{G73} H H H
L_{A638} H R^{G131} CD_{3} H H H L_{A1878} H H R^{G74} H H H
L_{A639} H R^{G132} CD_{3} H H H L_{A1879} H H R^{G75} H H H
L_{A640} H R^{G133} CD_{3} H H H L_{A1880} H H R^{G76} H H H
L_{A641} H R^{G134} CD_{3} H H H L_{A1881} H H R^{G77} H H H
L_{A642} H R^{G135} CD_{3} H H H L_{A1882} H H R^{G78} H H H
L_{A643} H R^{G136} CD_{3} H H H L_{A1883} H H R^{G79} H H H
L_{A644} H R^{G137} CD_{3} H H H L_{A1884} H H R^{G80} H H H
L_{A645} H R^{G133} CD_{3} H H H L_{A1885} H H R^{G81} H H H
L_{A646} H R^{G139} CD_{3} H H H L_{A1886} H H R^{G82} H H H
L_{A647} H R^{G140} CD_{3} H H H L_{A1887} H H R^{G83} H H H
L_{A648} H R^{G141} CD_{3} H H H L_{A1888} H H R^{G84} H H H
L_{A649} H R^{G142} CD_{3} H H H L_{A1889} H H R^{G85} H H H
L_{A650} H R^{G143} CD_{3} H H H L_{A1890} H H R^{G86} H H H
L_{A651} H R^{G144} CD_{3} H H H L_{A1891} H H R^{G87} H H H
L_{A652} H R^{G145} CD_{3} H H H L_{A1892} H H R^{G88} H H H
Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6} Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6}
L_{A653} H R^{G146} CD_{3} H H H L_{A1893} H H R^{G89} H H H
L_{A654} H R^{G147} CD_{3} H H H L_{A1894} H H R^{G90} H H H
L_{A655} H R^{G148} CD_{3} H H H L_{A1895} H H R^{G91} H H H
L_{A656} H R^{G149} CD_{3} H H H L_{A1896} H H R^{G92} H H H
L_{A657} H R^{G150} CD_{3} H H H L_{A1897} H H R^{G93} H H H
L_{A658} H R^{G151} CD_{3} H H H L_{A1898} H H R^{G94} H H H
L_{A659} H R^{G152} CD_{3} H H H L_{A1899} H H R^{G95} H H H
L_{A660} H R^{G153} CD_{3} H H H L_{A1900} H H R^{G96} H H H
L_{A661} H R^{G154} CD_{3} H H H L_{A1901} H H R^{G97} H H H
L_{A662} H R^{G155} CD_{3} H H H L_{A1902} H H R^{G98} H H H
L_{A663} H R^{G156} CD_{3} H H H L_{A1903} H H R^{G99} H H H
L_{A664} H R^{G157} CD_{3} H H H L_{A1904} H H R^{G100} H H H
L_{A665} H R^{G158} CD_{3} H H H L_{A1905} H H R^{G101} H H H
L_{A666} H R^{G159} CD_{3} H H H L_{A1906} H H R^{G102} H H H
L_{A667} H R^{G160} CD_{3} H H H L_{A1907} H H R^{G103} H H H
L_{A668} H R^{G161} CD_{3} H H H L_{A1908} H H R^{G104} H H H
L_{A669} H R^{G162} CD_{3} H H H L_{A1909} H H R^{G105} H H H
L_{A670} H R^{G163} CD_{3} H H H L_{A1910} H H R^{G106} H H H
L_{A671} H R^{G164} CD_{3} H H H L_{A1911} H H R^{G107} H H H
L_{A672} H R^{G165} CD_{3} H H H L_{A1912} H H R^{G108} H H H
L_{A673} H R^{G166} CD_{3} H H H L_{A1913} H H R^{G109} H H H
L_{A674} H R^{G167} CD_{3} H H H L_{A1914} H H R^{G110} H H H
L_{A675} H R^{G168} CD_{3} H H H L_{A1915} H H R^{G111} H H H
L_{A676} H R^{G169} CD_{3} H H H L_{A1916} H H R^{G112} H H H
Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6} Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6}
L_{A677} CD3 R^{G1} CD_{3} H H CD_{3} L_{A1917} H H R^{G113} H H H
L_{A678} CD3 R^{G2} CD_{3} H H CD_{3} L_{A1918} H H R^{G114} H H H
L_{A679} CD3 R^{G3} CD_{3} H H CD_{3} L_{A1919} H H R^{G115} H H H
L_{A680} CD3 R^{G4} CD_{3} H H CD_{3} L_{A1920} H H R^{G116} H H H
L_{A681} CD3 R^{G5} CD_{3} H H CD_{3} L_{A1921} H H R^{G117} H H H
L_{A682} CD3 R^{G6} CD_{3} H H CD_{3} L_{A1922} H H R^{G118} H H H
L_{A683} CD3 R^{G7} CD_{3} H H CD_{3} L_{A1923} H H R^{G119} H H H
L_{A684} CD3 R^{G8} CD_{3} H H CD_{3} L_{A1924} H H R^{G120} H H H
L_{A685} CD3 R^{G9} CD_{3} H H CD_{3} L_{A1925} H H R^{G121} H H H
L_{A686} CD3 R^{G10} CD_{3} H H CD_{3} L_{A1926} H H R^{G122} H H H
L_{A687} CD3 R^{G11} CD_{3} H H CD_{3} L_{A1927} H H R^{G123} H H H
L_{A688} CD3 R^{G12} CD_{3} H H CD_{3} L_{A1928} H H R^{G124} H H H
L_{A689} CD3 R^{G13} CD_{3} H H CD_{3} L_{A1929} H H R^{G125} H H H
L_{A690} CD3 R^{G14} CD_{3} H H CD_{3} L_{A1930} H H R^{G126} H H H
L_{A691} CD3 R^{G15} CD_{3} H H CD_{3} L_{A1931} H H R^{G127} H H H
L_{A692} CD3 R^{G16} CD_{3} H H CD_{3} L_{A1932} H H R^{G128} H H H
L_{A693} CD3 R^{G17} CD_{3} H H CD_{3} L_{A1933} H H R^{G129} H H H
L_{A694} CD3 R^{G18} CD_{3} H H CD_{3} L_{A1934} H H R^{G130} H H H
L_{A695} CD3 R^{G19} CD_{3} H H CD_{3} L_{A1935} H H R^{G131} H H H
L_{A696} CD3 R^{G20} CD_{3} H H CD_{3} L_{A1936} H H R^{G132} H H H
L_{A697} CD3 R^{G21} CD_{3} H H CD_{3} L_{A1937} H H R^{G133} H H H
L_{A698} CD3 R^{G22} CD_{3} H H CD_{3} L_{A1938} H H R^{G134} H H H
L_{A699} CD3 R^{G23} CD_{3} H H CD_{3} L_{A1939} H H R^{G135} H H H
L_{A700} CD3 R^{G24} CD_{3} H H CD_{3} L_{A1940} H H R^{G136} H H H
Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6} Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6}
L_{A701} CD3 R^{G25} CD_{3} H H CD_{3} L_{A1941} H H R^{G137} H H H
L_{A702} CD_{3} R^{G26} CD_{3} H H CD_{3} L_{A1942} H H R^{G138} H H H
L_{A703} CD_{3} R^{G27} CD_{3} H H CD_{3} L_{A1943} H H R^{G139} H H H
L_{A704} CD_{3} R^{G28} CD_{3} H H CD_{3} L_{A1944} H H R^{G140} H H H
L_{A705} CD_{3} R^{G29} CD_{3} H H CD_{3} L_{A1945} H H R^{G141} H H H
L_{A706} CD_{3} R^{G30} CD_{3} H H CD_{3} L_{A1946} H H R^{G142} H H H
L_{A707} CD_{3} R^{G31} CD_{3} H H CD_{3} L_{A1947} H H R^{G143} H H H
L_{A708} CD_{3} R^{G32} CD_{3} H H CD_{3} L_{A1948} H H R^{G144} H H H
L_{A709} CD_{3} R^{G33} CD_{3} H H CD_{3} L_{A1949} H H R^{G145} H H H
L_{A710} CD_{3} R^{G34} CD_{3} H H CD_{3} L_{A1950} H H R^{G146} H H H
L_{A711} CD_{3} R^{G35} CD_{3} H H CD_{3} L_{A1951} H H R^{G147} H H H
L_{A712} CD_{3} R^{G36} CD_{3} H H CD_{3} L_{A1952} H H R^{G148} H H H
L_{A713} CD_{3} R^{G37} CD_{3} H H CD_{3} L_{A1953} H H R^{G149} H H H
L_{A714} CD_{3} R^{G38} CD_{3} H H CD_{3} L_{A1954} H H R^{G150} H H H
L_{A715} CD_{3} R^{G39} CD_{3} H H CD_{3} L_{A1955} H H R^{G151} H H H
L_{A716} CD_{3} R^{G40} CD_{3} H H CD_{3} L_{A1956} H H R^{G152} H H H
L_{A717} CD_{3} R^{G41} CD_{3} H H CD_{3} L_{A1957} H H R^{G153} H H H
L_{A718} CD_{3} R^{G42} CD_{3} H H CD_{3} L_{A1958} H H R^{G154} H H H
L_{A719} CD_{3} R^{G43} CD_{3} H H CD_{3} L_{A1959} H H R^{G155} H H H
L_{A720} CD_{3} R^{G44} CD_{3} H H CD_{3} L_{A1960} H H R^{G156} H H H
L_{A721} CD_{3} R^{G45} CD_{3} H H CD_{3} L_{A1961} H H R^{G157} H H H
L_{A722} CD_{3} R^{G46} CD_{3} H H CD_{3} L_{A1962} H H R^{G158} H H H
L_{A723} CD_{3} R^{G47} CD_{3} H H CD_{3} L_{A1963} H H R^{G159} H H H
L_{A724} CD_{3} R^{G48} CD_{3} H H CD_{3} L_{A1964} H H R^{G160} H H H
Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6} Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6}
L_{A725} CD_{3} R^{G49} CD_{3} H H CD_{3} L_{A1965} H H R^{G161} H H H
L_{A726} CD_{3} R^{G50} CD_{3} H H CD_{3} L_{A1966} H H R^{G162} H H H
L_{A727} CD_{3} R^{G51} CD_{3} H H CD_{3} L_{A1967} H H R^{G163} H H H
L_{A728} CD_{3} R^{G52} CD_{3} H H CD_{3} L_{A1968} H H R^{G164} H H H
L_{A729} CD_{3} R^{G53} CD_{3} H H CD_{3} L_{A1969} H H R^{G165} H H H
L_{A730} CD_{3} R^{G54} CD_{3} H H CD_{3} L_{A1970} H H R^{G166} H H H
L_{A731} CD_{3} R^{G55} CD_{3} H H CD_{3} L_{A1971} H H R^{G167} H H H
L_{A732} CD_{3} R^{G56} CD_{3} H H CD_{3} L_{A1972} H H R^{G168} H H H
L_{A733} CD_{3} R^{G57} CD_{3} H H CD_{3} L_{A1973} H H R^{G169} H H H
L_{A734} CD_{3} R^{GS8} CD_{3} H H CD_{3} L_{A1974} H H H R^{G1} H H
L_{A735} CD_{3} R^{G59} CD_{3} H H CD_{3} L_{A1975} H H H R^{G2} H H
L_{A736} CD_{3} R^{G60} CD_{3} H H CD_{3} L_{A1976} H H H R^{G3} H H
L_{A737} CD_{3} R^{G61} CD_{3} H H CD_{3} L_{A1977} H H H R^{G4} H H
L_{A738} CD_{3} R^{G62} CD_{3} H H CD_{3} L_{A1978} H H H R^{G5} H H
L_{A739} CD_{3} R^{G63} CD_{3} H H CD_{3} L_{A1979} H H H R^{G6} H H
L_{A740} CD_{3} R^{G64} CD_{3} H H CD_{3} L_{A1980} H H H R^{G7} H H
L_{A741} CD_{3} R^{G65} CD_{3} H H CD_{3} L_{A1981} H H H R^{G8} H H
L_{A742} CD_{3} R^{G66} CD_{3} H H CD_{3} L_{A1982} H H H R^{G9} H H
L_{A743} CD_{3} R^{G67} CD_{3} H H CD_{3} L_{A1983} H H H R^{G10} H H
L_{A744} CD_{3} R^{G68} CD_{3} H H CD_{3} L_{A1984} H H H R^{G11} H H
L_{A745} CD_{3} R^{G69} CD_{3} H H CD_{3} L_{A1985} H H H R^{G12} H H
L_{A746} CD_{3} R^{G70} CD_{3} H H CD_{3} L_{A1986} H H H R^{G13} H H
L_{A747} CD_{3} R^{G71} CD_{3} H H CD_{3} L_{A1987} H H H R^{G14} H H
L_{A748} CD_{3} R^{G72} CD_{3} H H CD_{3} L_{A1988} H H H R^{G15} H H
Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6} Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6}
L_{A749} CD_{3} R^{G73} CD_{3} H H CD_{3} L_{A1989} H H H R^{G16} H H
L_{A750} CD_{3} R^{G74} CD_{3} H H CD_{3} L_{A1990} H H H R^{G17} H H
L_{A751} CD_{3} R^{G75} CD_{3} H H CD_{3} L_{A1991} H H H R^{G18} H H
L_{A752} CD_{3} R^{G76} CD_{3} H H CD_{3} L_{A1992} H H H R^{G19} H H
L_{A753} CD_{3} R^{G77} CD_{3} H H CD_{3} L_{A1993} H H H R^{G20} H H
L_{A754} CD_{3} R^{G78} CD_{3} H H CD_{3} L_{A1994} H H H R^{G21} H H
L_{A755} CD_{3} R^{G79} CD_{3} H H CD_{3} L_{A1995} H H H R^{G22} H H
L_{A756} CD_{3} R^{G80} CD_{3} H H CD_{3} L_{A1996} H H H R^{G23} H H
L_{A757} CD_{3} R^{G81} CD_{3} H H CD_{3} L_{A1997} H H H R^{G24} H H
L_{A758} CD_{3} R^{G82} CD_{3} H H CD_{3} L_{A1998} H H H R^{G25} H H
L_{A759} CD_{3} R^{G83} CD_{3} H H CD_{3} L_{A1999} H H H R^{G26} H H
L_{A760} CD_{3} R^{G84} CD_{3} H H CD_{3} L_{A2000} H H H R^{G27} H H
L_{A761} CD_{3} R^{G85} CD_{3} H H CD_{3} L_{A2001} H H H R^{G28} H H
L_{A762} CD_{3} R^{G86} CD_{3} H H CD_{3} L_{A2002} H H H R^{G29} H H
L_{A763} CD_{3} R^{G87} CD_{3} H H CD_{3} L_{A2003} H H H R^{G30} H H
L_{A764} CD_{3} R^{G88} CD_{3} H H CD_{3} L_{A2004} H H H R^{G31} H H
L_{A765} CD_{3} R^{G89} CD_{3} H H CD_{3} L_{A2005} H H H R^{G32} H H
L_{A766} CD_{3} R^{G90} CD_{3} H H CD_{3} L_{A2006} H H H R^{G33} H H
L_{A767} CD_{3} R^{G91} CD_{3} H H CD_{3} L_{A2007} H H H R^{G34} H H
L_{A768} CD_{3} R^{G92} CD_{3} H H CD_{3} L_{A2008} H H H R^{G35} H H
L_{A769} CD_{3} R^{G93} CD_{3} H H CD_{3} L_{A2009} H H H R^{G36} H H
L_{A770} CD_{3} R^{G94} CD_{3} H H CD_{3} L_{A2010} H H H R^{G37} H H
L_{A771} CD_{3} R^{G95} CD_{3} H H CD_{3} L_{A2011} H H H R^{G38} H H
L_{A772} CD_{3} R^{G96} CD_{3} H H CD_{3} L_{A2012} H H H R^{G39} H H
Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6} Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6}
L_{A773} CD_{3} R^{G97} CD_{3} H H CD_{3} L_{A2013} H H H R^{G40} H H
L_{A774} CD_{3} R^{G98} CD_{3} H H CD_{3} L_{A2014} H H H R^{G41} H H
L_{A775} CD_{3} R^{G99} CD_{3} H H CD_{3} L_{A2015} H H H R^{G42} H H
L_{A776} CD_{3} R^{G100} CD_{3} H H CD_{3} L_{A2016} H H H R^{G43} H H
L_{A777} CD_{3} R^{G101} CD_{3} H H CD_{3} L_{A2017} H H H R^{G44} H H
L_{A778} CD_{3} R^{G102} CD_{3} H H CD_{3} L_{A2018} H H H R^{G45} H H
L_{A779} CD_{3} R^{G103} CD_{3} H H CD_{3} L_{A2019} H H H R^{G46} H H
L_{A780} CD_{3} R^{G104} CD_{3} H H CD_{3} L_{A2020} H H H R^{G47} H H
L_{A781} CD_{3} R^{G105} CD_{3} H H CD_{3} L_{A2021} H H H R^{G48} H H
L_{A782} CD_{3} R^{G106} CD_{3} H H CD_{3} L_{A2022} H H H R^{G49} H H
L_{A783} CD_{3} R^{G107} CD_{3} H H CD_{3} L_{A2023} H H H R^{G50} H H
L_{A784} CD_{3} R^{G108} CD_{3} H H CD_{3} L_{A2024} H H H R^{G51} H H
L_{A785} CD_{3} R^{G109} CD_{3} H H CD_{3} L_{A2025} H H H R^{G52} H H
L_{A786} CD_{3} R^{G110} CD_{3} H H CD_{3} L_{A2026} H H H R^{G53} H H
L_{A787} CD_{3} R^{G111} CD_{3} H H CD_{3} L_{A2027} H H H R^{G54} H H
L_{A788} CD_{3} R^{G112} CD_{3} H H CD_{3} L_{A2028} H H H R^{G55} H H
L_{A789} CD_{3} R^{G113} CD_{3} H H CD_{3} L_{A2029} H H H R^{G56} H H
L_{A790} CD_{3} R^{G114} CD_{3} H H CD_{3} L_{A2030} H H H R^{G57} H H
L_{A791} CD_{3} R^{G115} CD_{3} H H CD_{3} L_{A2031} H H H R^{GS8} H H
L_{A792} CD_{3} R^{G116} CD_{3} H H CD_{3} L_{A2032} H H H R^{G59} H H
L_{A793} CD_{3} R^{G117} CD_{3} H H CD_{3} L_{A2033} H H H R^{G60} H H
L_{A794} CD_{3} R^{G118} CD_{3} H H CD_{3} L_{A2034} H H H R^{G61} H H
L_{A795} CD_{3} R^{G119} CD_{3} H H CD_{3} L_{A2035} H H H R^{G62} H H
L_{A796} CD_{3} R^{G120} CD_{3} H H CD_{3} L_{A2036} H H H R^{G63} H H
Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6} Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6}
L_{A797} CD_{3} R^{G121} CD_{3} H H CD_{3} L_{A2037} H H H R^{G64} H H
L_{A798} CD_{3} R^{G122} CD_{3} H H CD_{3} L_{A2038} H H H R^{G65} H H
L_{A799} CD_{3} R^{G123} CD_{3} H H CD_{3} L_{A2039} H H H R^{G66} H H
L_{A800} CD_{3} R^{G124} CD_{3} H H CD_{3} L_{A2040} H H H R^{G67} H H
L_{A801} CD_{3} R^{G125} CD_{3} H H CD_{3} L_{A2041} H H H R^{G68} H H
L_{A802} CD_{3} R^{G126} CD_{3} H H CD_{3} L_{A2042} H H H R^{G69} H H
L_{A803} CD_{3} R^{G127} CD_{3} H H CD_{3} L_{A2043} H H H R^{G70} H H
L_{A804} CD_{3} R^{G128} CD_{3} H H CD_{3} L_{A2044} H H H R^{G71} H H
L_{A805} CD_{3} R^{G129} CD_{3} H H CD_{3} L_{A2045} H H H R^{G72} H H
L_{A806} CD_{3} R^{G130} CD_{3} H H CD_{3} L_{A2046} H H H R^{G73} H H
L_{A807} CD_{3} R^{G131} CD_{3} H H CD_{3} L_{A2047} H H H R^{G74} H H
L_{A808} CD_{3} R^{G132} CD_{3} H H CD_{3} L_{A2048} H H H R^{G75} H H
L_{A809} CD_{3} R^{G133} CD_{3} H H CD_{3} L_{A2049} H H H R^{G76} H H
L_{A810} CD_{3} R^{G134} CD_{3} H H CD_{3} L_{A2050} H H H R^{G77} H H
L_{A811} CD_{3} R^{G135} CD_{3} H H CD_{3} L_{A2051} H H H R^{G78} H H
L_{A812} CD_{3} R^{G136} CD_{3} H H CD_{3} L_{A2052} H H H R^{G79} H H
L_{A813} CD_{3} R^{G137} CD_{3} H H CD_{3} L_{A2053} H H H R^{G80} H H
L_{A814} CD_{3} R^{G138} CD_{3} H H CD_{3} L_{A2054} H H H R^{G81} H H
L_{A815} CD_{3} R^{G139} CD_{3} H H CD_{3} L_{A2055} H H H R^{G82} H H
L_{A816} CD_{3} R^{G140} CD_{3} H H CD_{3} L_{A2056} H H H R^{G83} H H
L_{A817} CD_{3} R^{G141} CD_{3} H H CD_{3} L_{A2057} H H H R^{G84} H H
L_{A818} CD_{3} R^{G142} CD_{3} H H CD_{3} L_{A2058} H H H R^{G85} H H
L_{A819} CD_{3} R^{G143} CD_{3} H H CD_{3} L_{A2059} H H H R^{G86} H H
L_{A820} CD_{3} R^{G144} CD_{3} H H CD_{3} L_{A2060} H H H R^{G87} H H
Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6} Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6}
L_{A821} CD_{3} R^{G145} CD_{3} H H CD_{3} L_{A2061} H H H R^{G88} H H
L_{A822} CD_{3} R^{G146} CD_{3} H H CD_{3} L_{A2062} H H H R^{G89} H H
L_{A823} CD_{3} R^{G147} CD_{3} H H CD_{3} L_{A2063} H H H R^{G90} H H
L_{A824} CD_{3} R^{G148} CD_{3} H H CD_{3} L_{A2064} H H H R^{G91} H H
L_{A825} CD_{3} R^{G149} CD_{3} H H CD_{3} L_{A2065} H H H R^{G92} H H
L_{A826} CD_{3} R^{G150} CD_{3} H H CD_{3} L_{A2066} H H H R^{G93} H H
L_{A827} CD_{3} R^{G151} CD_{3} H H CD_{3} L_{A2067} H H H R^{G94} H H
L_{A828} CD_{3} R^{G152} CD_{3} H H CD_{3} L_{A2068} H H H R^{G95} H H
L_{A829} CD_{3} R^{G153} CD_{3} H H CD_{3} L_{A2069} H H H R^{G96} H H
L_{A830} CD_{3} R^{G154} CD_{3} H H CD_{3} L_{A2070} H H H R^{G97} H H
L_{A831} CD_{3} R^{G155} CD_{3} H H CD_{3} L_{A2071} H H H R^{G98} H H
L_{A832} CD_{3} R^{G156} CD_{3} H H CD_{3} L_{A2072} H H H R^{G99} H H
L_{A833} CD_{3} R^{G157} CD_{3} H H CD_{3} L_{A2073} H H H R^{G100} H H
L_{A834} CD_{3} R^{G158} CD_{3} H H CD_{3} L_{A2074} H H H R^{G101} H H
L_{A835} CD_{3} R^{G159} CD_{3} H H CD_{3} L_{A2075} H H H R^{G102} H H
L_{A836} CD_{3} R^{G160} CD_{3} H H CD_{3} L_{A2076} H H H R^{G103} H H
L_{A837} CD_{3} R^{G161} CD_{3} H H CD_{3} L_{A2077} H H H R^{G104} H H
L_{A838} CD_{3} R^{G162} CD_{3} H H CD_{3} L_{A2078} H H H R^{G105} H H
L_{A839} CD_{3} R^{G163} CD_{3} H H CD_{3} L_{A2079} H H H R^{G106} H H
L_{A840} CD_{3} R^{G164} CD_{3} H H CD_{3} L_{A2080} H H H R^{G107} H H
L_{A841} CD_{3} R^{G165} CD_{3} H H CD_{3} L_{A2081} H H H R^{G108} H H
L_{A842} CD_{3} R^{G166} CD_{3} H H CD_{3} L_{A2082} H H H R^{G109} H H
L_{A843} CD_{3} R^{G167} CD_{3} H H CD_{3} L_{A2083} H H H R^{G110} H H
L_{A844} CD_{3} R^{G168} CD_{3} H H CD_{3} L_{A2084} H H H R^{G111} H H
Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6} Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6}
L_{A845} CD_{3} R^{G169} CD_{3} H H CD_{3} L_{A2085} H H H R^{G112} H H
L_{A846} CD_{3} R^{G1} CD_{3} H H H L_{A2086} H H H R^{G113} H H
L_{A847} CD_{3} R^{G2} CD_{3} H H H L_{A2087} H H H R^{G114} H H
L_{A848} CD_{3} R^{G3} CD_{3} H H H L_{A2088} H H H R^{G115} H H
L_{A849} CD_{3} R^{G4} CD_{3} H H H L_{A2089} H H H R^{G116} H H
L_{A850} CD_{3} R^{G5} CD_{3} H H H L_{A2090} H H H R^{G117} H H
L_{A851} CD_{3} R^{G6} CD_{3} H H H L_{A2091} H H H R^{G118} H H
L_{A852} CD_{3} R^{G7} CD_{3} H H H L_{A2092} H H H R^{G119} H H
L_{A853} CD_{3} R^{G8} CD_{3} H H H L_{A2093} H H H R^{G120} H H
L_{A854} CD_{3} R^{G9} CD_{3} H H H L_{A2094} H H H R^{G121} H H
L_{A855} CD_{3} R^{G10} CD_{3} H H H L_{A2095} H H H R^{G122} H H
L_{A856} CD_{3} R^{G11} CD_{3} H H H L_{A2096} H H H R^{G123} H H
L_{A857} CD_{3} R^{G12} CD_{3} H H H L_{A2097} H H H R^{G124} H H
L_{A858} CD_{3} R^{G13} CD_{3} H H H L_{A2098} H H H R^{G125} H H
L_{A859} CD_{3} R^{G14} CD_{3} H H H L_{A2099} H H H R^{G126} H H
L_{A860} CD_{3} R^{G15} CD_{3} H H H L_{A2100} H H H R^{G127} H H
L_{A861} CD_{3} R^{G16} CD_{3} H H H L_{A2101} H H H R^{G128} H H
L_{A862} CD_{3} R^{G17} CD_{3} H H H L_{A2102} H H H R^{G129} H H
L_{A863} CD_{3} R^{G18} CD_{3} H H H L_{A2103} H H H R^{G130} H H
L_{A864} CD_{3} R^{G19} CD_{3} H H H L_{A2104} H H H R^{G131} H H
L_{A865} CD_{3} R^{G20} CD_{3} H H H L_{A2105} H H H R^{G132} H H
L_{A866} CD_{3} R^{G21} CD_{3} H H H L_{A2106} H H H R^{G133} H H
L_{A867} CD_{3} R^{G22} CD_{3} H H H L_{A2107} H H H R^{G134} H H
L_{A868} CD_{3} R^{G23} CD_{3} H H H L_{A2108} H H H R^{G135} H H
Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6} Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6}
L_{A869} CD_{3} R^{G24} CD_{3} H H H L_{A2109} H H H R^{G136} H H
L_{A870} CD_{3} R^{G25} CD_{3} H H H L_{A2110} H H H R^{G137} H H
L_{A871} CD_{3} R^{G26} CD_{3} H H H L_{A2111} H H H R^{G138} H H
L_{A872} CD_{3} R^{G27} CD_{3} H H H L_{A2112} H H H R^{G139} H H
L_{A873} CD_{3} R^{G28} CD_{3} H H H L_{A2113} H H H R^{G140} H H
L_{A874} CD_{3} R^{G29} CD_{3} H H H L_{A2114} H H H R^{G141} H H
L_{A875} CD_{3} R^{G30} CD_{3} H H H L_{A2115} H H H R^{G142} H H
L_{A876} CD_{3} R^{G31} CD_{3} H H H L_{A2116} H H H R^{G143} H H
L_{A877} CD_{3} R^{G32} CD_{3} H H H L_{A2117} H H H R^{G144} H H
L_{A878} CD_{3} R^{G33} CD_{3} H H H L_{A2118} H H H R^{G145} H H
L_{A879} CD_{3} R^{G34} CD_{3} H H H L_{A2119} H H H R^{G146} H H
L_{A880} CD_{3} R^{G35} CD_{3} H H H L_{A2120} H H H R^{G147} H H
L_{A881} CD_{3} R^{G36} CD_{3} H H H L_{A2121} H H H R^{G148} H H
L_{A882} CD_{3} R^{G37} CD_{3} H H H L_{A2122} H H H R^{G149} H H
L_{A883} CD_{3} R^{G38} CD_{3} H H H L_{A2123} H H H R^{G150} H H
L_{A884} CD_{3} R^{G39} CD_{3} H H H L_{A2124} H H H R^{G151} H H
L_{A885} CD_{3} R^{G40} CD_{3} H H H L_{A2125} H H H R^{G152} H H
L_{A886} CD_{3} R^{G41} CD_{3} H H H L_{A2126} H H H R^{G153} H H
L_{A887} CD_{3} R^{G42} CD_{3} H H H L_{A2127} H H H R^{G154} H H
L_{A888} CD_{3} R^{G43} CD_{3} H H H L_{A2128} H H H R^{G155} H H
L_{A889} CD_{3} R^{G44} CD_{3} H H H L_{A2129} H H H R^{G156} H H
L_{A890} CD_{3} R^{G45} CD_{3} H H H L_{A2130} H H H R^{G157} H H
L_{A891} CD_{3} R^{G46} CD_{3} H H H L_{A2131} H H H R^{G158} H H
L_{A892} CD_{3} R^{G47} CD_{3} H H H L_{A2132} H H H R^{G159} H H
Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6} Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6}
L_{A893} CD_{3} R^{G48} CD_{3} H H H L_{A2133} H H H R^{G160} H H
L_{A894} CD_{3} R^{G49} CD_{3} H H H L_{A2134} H H H R^{G161} H H
L_{A895} CD_{3} R^{G50} CD_{3} H H H L_{A2135} H H H R^{G162} H H
L_{A896} CD_{3} R^{G51} CD_{3} H H H L_{A2136} H H H R^{G163} H H
L_{A897} CD_{3} R^{G52} CD_{3} H H H L_{A2137} H H H R^{G164} H H
L_{A898} CD_{3} R^{G53} CD_{3} H H H L_{A2138} H H H R^{G165} H H
L_{A899} CD_{3} R^{G54} CD_{3} H H H L_{A2139} H H H R^{G166} H H
L_{A900} CD_{3} R^{G55} CD_{3} H H H L_{A2140} H H H R^{G167} H H
L_{A901} CD_{3} R^{G56} CD_{3} H H H L_{A2141} H H H R^{G168} H H
L_{A902} CD_{3} R^{G57} CD_{3} H H H L_{A2142} H H H R^{G169} H H
L_{A903} CD_{3} R^{G58} CD_{3} H H H L_{A2143} H H H H R^{G1} H
L_{A904} CD_{3} R^{G59} CD_{3} H H H L_{A2144} H H H H R^{G2} H
L_{A905} CD_{3} R^{G60} CD_{3} H H H L_{A2145} H H H H R^{G3} H
L_{A906} CD_{3} R^{G61} CD_{3} H H H L_{A2146} H H H H R^{G4} H
L_{A907} CD_{3} R^{G62} CD_{3} H H H L_{A2147} H H H H R^{G5} H
L_{A908} CD_{3} R^{G63} CD_{3} H H H L_{A2148} H H H H R^{G6} H
L_{A909} CD_{3} R^{G64} CD_{3} H H H L_{A2149} H H H H R^{G7} H
L_{A910} CD_{3} R^{G65} CD_{3} H H H L_{A2150} H H H H R^{G8} H
L_{A911} CD_{3} R^{G66} CD_{3} H H H L_{A2151} H H H H R^{G9} H
L_{A912} CD_{3} R^{G67} CD_{3} H H H L_{A2152} H H H H R^{G10} H
L_{A913} CD_{3} R^{G68} CD_{3} H H H L_{A2153} H H H H R^{G11} H
L_{A914} CD_{3} R^{G69} CD_{3} H H H L_{A2154} H H H H R^{G12} H
L_{A915} CD_{3} R^{G70} CD_{3} H H H L_{A2155} H H H H R^{G13} H
L_{A916} CD_{3} R^{G71} CD_{3} H H H L_{A2156} H H H H R^{G14} H
Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6} Ligand R_{A1} R_{A2} R_{A3} R_{A4} R_{A5} R_{A6}
L_{A917} CD_{3} R^{G72} CD_{3} H H H L_{A2157} H H H H R^{G15} H
L_{A918} CD_{3} R^{G73} CD_{3} H H H L_{A2158} H H H H R^{G16} H
L_{A919} CD_{3} R^{G74} CD_{3} H H H L_{A2159} H H H H R^{G17} H
L_{A920} CD_{3} R^{G75} CD_{3} H H H L_{A2160} H H H H R^{G18} H
L_{A921} CD_{3} R^{G76} CD_{3} H H H L_{A2161} H H H H R^{G19} H
L_{A922} CD_{3} R^{G77} CD_{3} H H H L_{A2162} H H H H R^{G20} H
L_{A923} CD_{3} R^{G78} CD_{3} H H H L_{A2163} H H H H R^{G21} H
L_{A924} CD_{3} R^{G79} CD_{3} H H H L_{A2164} H H H H R^{G22} H
L_{A925} CD_{3} R^{G80} CD_{3} H H H L_{A2165} H H H H R^{G23}