Abstract: A method is provided to promote secretion of cholecystokinin (CCK) by administering an active component. The active component includes acrylic acid and/or an unsaturated aldehyde having a main chain of 4 to 12 carbon atoms having a double bond in at least position 2 or 4, where the main chain has 4 to 9 carbon atoms when there is a double bond in only position 2, and the main chain has 9 to 12 carbon atoms when there is a double bond in only position 4. The cholecystokinin secretion-promoting composition can be used as an appetite suppressant. By adding this cholecystokinin secretion-promoting composition to food, appetite-suppressing food products can be provided.
Abstract: The inventive subject matter relates to compounds of Formula I, compositions thereof, and processes for making such compounds as further described herein. The inventive compounds and compositions have antimicrobial properties and are useful as environmental disinfectants, topical cleansers such as topical personal care compositions, sanitizers, preservatives, in water treatment, as permanent or erodible coatings for medical devices and appliances, and in therapeutics. Additionally, the compounds of Formula I will serve as synthetic intermediates for making additional novel derivatives of triscationic amphiphile compounds.
Abstract: A biphenyl diester useful as a plasticizer having the formula (I): wherein R1 is an alkyl group having 5 to 15 carbon atoms and R2 is a methyl group or a phenyl group.
Type:
Grant
Filed:
May 27, 2015
Date of Patent:
January 31, 2017
Assignee:
ExxonMobil Chemical Patents Inc.
Inventors:
Jihad M. Dakka, Wei Tang, Stephen Zushma, Christine A. Costello, Diana Smirnova, Madhavi Vadlamudi, Victor DeFlorio
Abstract: In a process for producing methyl-substituted biphenyl compounds, a feed comprising at least one aromatic hydrocarbon selected from the group consisting of toluene, xylene and mixtures thereof is contacted with hydrogen in the presence of a hydroalkylation catalyst under conditions effective to produce a hydroalkylation reaction product comprising (methylcyclohexyl)toluenes and/or (dimethylcyclohexyl)xylenes together with dialkylated C21+ compounds. At least part of the dialkylated C21+ compounds is then removed from the hydroalkylation reaction product to produce a dehydrogenation feed; and at least part of the dehydrogenation feed is dehydrogenated in the presence of a dehydrogenation catalyst under conditions effective to produce a dehydrogenation reaction product comprising a mixture of methyl-substituted biphenyl compounds.
Type:
Grant
Filed:
March 7, 2014
Date of Patent:
January 31, 2017
Assignee:
ExxonMobil Chemical Patents Inc.
Inventors:
Jihad M. Dakka, Lorenzo C. DeCaul, Victor DeFlorio
Abstract: The present invention discloses a process for depolymerization of lignin to yield substituted phenolic monomers using Brönsted ionic liquid as catalyst under mild reaction conditions to obtain an overall yield of monomers up to 97%.
Type:
Grant
Filed:
May 9, 2014
Date of Patent:
January 24, 2017
Assignee:
Council of Scientific and Industrial Research
Abstract: The present disclosure provides a process for synthesis of 3-aryl-2-hydroxy propanoic acid derivatives of formula (S)-1. wherein R1 represents H or (C1-C5) alkyl groups and R2 represents (C1-C5) alkyl groups.
Type:
Grant
Filed:
May 9, 2014
Date of Patent:
January 24, 2017
Assignee:
Council of Scientific and Industrial Research
Inventors:
Muthukrishnan Murugan, Mujahid Mohammad
Abstract: A catalyst is provided. The catalyst includes a carrier and a metal Pd. The carrier is represented by a formula: MxAl(1?x)O(3?x)/2, where M is an alkaline earth metal, and x is between 0.09 and 0.24. The metal Pd is loaded on the carrier. A method for manufacturing the catalyst and a method for manufacturing a hydrogenated bisphenol A or derivatives thereof using the catalyst are also provided.
Type:
Grant
Filed:
December 9, 2015
Date of Patent:
January 17, 2017
Assignee:
INDUSTRIAL TECHNOLOGY RESEARCH INSTITUTE
Abstract: Disclosed are inhibitors of the farnesoid X receptor, for example of formula (I), wherein R1, R2, R4, X, Y, Z, m, and n are as defined herein, which are useful in treating or preventing obesity, type 2 diabetes/insulin resistance and non alcoholic fatty liver disease in a mammal in need thereof. Also disclosed is a composition comprising a pharmaceutically suitable carrier and at least Cone compound of the invention, a method of method of inhibiting a farnesoid X receptor in a mammal, and a method of treating or preventing obesity in a mammal.
Type:
Grant
Filed:
August 1, 2014
Date of Patent:
January 10, 2017
Assignees:
The United States of America, as represented by the Secretary, Department of Health and Human Services, The Penn State Research Foundation
Inventors:
Frank J. Gonzalez, Changtao Jiang, Cen Xie, Andrew D. Patterson, Fei Li, James B. Mitchell
Abstract: The invention relates to the production of acrolein and/or acrylic acid from glycerol, and more particularly to a method for continuous production of a stream comprising acrolein by dehydration of glycerol, comprising cycles of reaction and regeneration of a dehydration catalyst.
Type:
Grant
Filed:
April 3, 2013
Date of Patent:
December 27, 2016
Assignee:
Arkema France
Inventors:
Jean-Francois Devaux, Michel Fauconet, Nabil Tlili
Abstract: The daurinol compound according to the present invention exhibits excellent therapeutic effects on arthritis and inflammatory bowel diseases by having an excellent activity in inhibiting the generation of IL-17 and TNF-?, which are inflammatory cytokines causing inflammation, and can alleviate transplant rejection by inhibiting the proliferation of alloreactive T cells and increasing regulatory T cells; therefore, the daurinol compound according to the present invention can be used as a pharmaceutical composition capable of treating and preventing immune diseases. In addition, being a natural substance derived from the Mongolian medicinal plant Haplophyllum dauricum or Haplophyllum cappadocicum, the daurinol compound according to the present invention does not cause cytotoxicity and thus may be used as a composition for a functional health food capable of preventing and remedying immune diseases.
Type:
Grant
Filed:
August 22, 2014
Date of Patent:
December 27, 2016
Assignee:
THE CATHOLIC UNIVERSITY OF KOREA INDUSTRY-ACADEMIC COOPERATION FOUNDATION, CATHOLIC UNIV. OF KOREA SONGEUI CAMPUS
Inventors:
Mi-La Cho, Dong-Yun Shin, Min-Jung Park, Seon-Yeong Lee, Eun Ji Yang, Eun Kyung Kim, Hye-Jin Son, Eun-Jung Lee, Jae-Kyung Kim, Sung-Hee Lee
Abstract: The present disclosure provides novel poly(phenylene ethynylene) (PPE) compounds, methods for synthesizing these compounds, and materials and substances incorporating these compounds. The various PPEs show antibacterial, antiviral and antifungal activity.
Type:
Grant
Filed:
July 13, 2011
Date of Patent:
December 27, 2016
Assignees:
STC.UNM, University of Florida Research Foundation, Inc.
Inventors:
David G. Whitten, Kirk S. Schanze, Anand Parthasarathy, Eunkyung Ji, Motokatsu Ogawa, Thomas S. Corbitt, Dimitri Dascier, Ying Wang, Linnea K. Ista, Eric H. Hill
Abstract: Tetrahydroprotoberbine (THPB) compounds and their use in the treatment of neurological, psychiatric and neurodegenerative diseases is provided. The compounds include d-govadine, l-govadine and racemic govadine, as well as d-THPBs of general formula (I). Enantioselective processes for preparing compounds of formula (I), and d- and l-govadine are also provided.
Type:
Grant
Filed:
August 2, 2012
Date of Patent:
December 27, 2016
Inventors:
James Jackson Miller, Anthony George Phillips, Christopher Court Lapish, Glenn Martin Sammis
Abstract: A ceramide dispersion composition, includes: at least one ceramide represented by Formula (1) or Formula (2); a surfactant; and trisodium ascorbyl palmitate phosphate, wherein in Formula (1), R1 represents an aliphatic hydrocarbon group having at least one unsaturated double bond, R2 represents an alkyl group having 9 or more carbon atoms, and n represents an integer from 20 to 34; and in Formula (2), R3 represents an aliphatic hydrocarbon group having at least one unsaturated double bond, R4 represents an alkyl group having 9 or more carbon atoms, m represents an integer from 20 to 34, and X represents a hydrogen atom or a hydroxyl group.
Abstract: The invention relates to compounds of the formula I. The compounds of formula I are versatile peptide intermediates for the solid phase peptide synthesis (SPPS) of peptide drugs which comprise a Glu-fatty alkyl side chain building block attached to a Lys-part of the peptide chain.
Abstract: A pharmaceutical composition is provided which includes perillyl alcohol conjugated with a therapeutic agent and further includes and a hydrolyzable acylated aliphatic tail. A method of using the pharmaceutical composition is also provided for treating a condition or disease of a patient, e.g., cancer.
Type:
Grant
Filed:
February 11, 2016
Date of Patent:
December 20, 2016
Assignee:
NeOnc Technologies, Inc.
Inventors:
Thomas Chen, Daniel Levin, Satish Pupalli
Abstract: This invention provides, among other things, tetrahydroisoquinolines useful for treating viral infections, pharmaceutical formulations containing such compounds, as well as methods of inhibiting the replication of a virus, such as HIV, or treating a disease, such as AIDS.
Type:
Grant
Filed:
December 15, 2015
Date of Patent:
December 13, 2016
Assignee:
Prosetta Antiviral Inc.
Inventors:
Andy Atuegbu, Dennis Solas, Clarence R. Hurt, Anatoliy Kitaygorodskyy
Abstract: Augmented or synergized anti-inflammatory constructs are disclosed including terpenes covalently conjugated with other anti-inflammatory molecules such as nonsteroidal anti-inflammatory drugs, vanilloids, amino acids and polyamines; and anti-inflammatory molecules covalently conjugated with specific amino acids. For the latter, further conjugation with a choline bioisostere further augments the anti-inflammatory activity.
Type:
Grant
Filed:
March 14, 2014
Date of Patent:
December 6, 2016
Assignees:
RUTGERS, THE STATE UNIVERSITY OF NEW JERSEY, LEHIGH UNIVERSITY
Inventors:
Jeffrey D. Laskin, Ned D. Heindel, Diane E. Heck, Carl Jeffrey Lacey, Sherri C. Young
Abstract: The disclosure provides new and improved methods for the Pd-catalyzed asymmetric ?-arylation of ester compounds, which produce the corresponding ?-aryl moiety in high enantioselectivity (generally >90% ee). The present methods utilize a palladium catalyst supported by new (R)—H8-BINOL-derived monophosphine ligands. The method is applicable to a wide variety of aryl triflate substrates having variations in both electronic and steric properties. These aryl triflate substrates react with various ?-alkyl (Z)- and/or (E)-0-trimethylsilyl ketene acetals in the presence of a Pd catalyst, (R)—H8-BINOL-derived monophosphine ligand, and a mild activator, for example, LiOAC, to provide the asymmetric ?-arylation of ester compounds in high ee.
Abstract: A method for producing xylylene diisocyanate includes a thermal decomposition step of thermally decomposing xylylene dicarbamate; a first separation step of separating, from the thermal decomposition product obtained in the thermal decomposition step, an isocyanate-containing component containing xylylene diisocyanate as a main component and an alcohol-containing component containing alcohol as a main component and containing xylylene diisocyanate as a subcomponent; a second separation step of separating xylylene dicarbamate and alcohol from the alcohol-containing component obtained in the first separation step; and a returning step of returning xylylene dicarbamate obtained in the second separation step to the thermal decomposition step.
Type:
Grant
Filed:
March 28, 2014
Date of Patent:
December 6, 2016
Assignee:
MITSUI CHEMICALS, INC.
Inventors:
Koji Takamatsu, Hideki Sone, Masaaki Sasaki
Abstract: Killing of bed bugs is accomplished by bringing the bed bugs into contact with a toxic amount of at least one of the compounds of the structure (I) wherein X is —OH, ?O, or —O(O)CR, wherein R is selected from H and a branched or straight chain, saturated or unsaturated hydrocarbyl group with zero to three double bonds and from 1 to 11 carbon atoms; R1 is H or CH3; R2 is H or CH3; R3 is H or a branched or straight chain, saturated or unsaturated hydrocarbyl group with zero to three double bonds and from 1 to 11 carbon atoms; and wherein the compounds of structure (I) contain from 6 to 20 total carbon atoms in the compounds.