Abstract: Provided in the present application are a compound represented by formula (I), a pharmaceutical composition containing the compound, and the use thereof. The compound represented by formula (I) of the present application has a good effect in terms of inhibiting the activity of HPK1.
Type:
Application
Filed:
November 3, 2021
Publication date:
October 12, 2023
Applicant:
BroadenBio Co., Ltd.
Inventors:
Gongping Duan, Xingmin Zhang, Zhihua Wang, Xianglong Wei, Min Li
Abstract: The present invention is directed to, in part, fused heteroaryl compounds and compositions useful for preventing and/or treating a disease or condition relating to aberrant function of a voltage-gated, sodium ion channel, for example, abnormal late/persistent sodium current. Methods of treating a disease or condition relating to aberrant function of a sodium ion channel including Dravet syndrome or epilepsy are also provided herein.
Type:
Application
Filed:
March 10, 2023
Publication date:
October 12, 2023
Inventors:
Kiran Reddy, Gabriel Martinez Botella, Andrew Mark Griffin, Brian Edward Marron
Abstract: The present disclosure provides a compound represented by structural Formula (I): or a pharmaceutically acceptable salt thereof useful for treating a cancer.
Type:
Application
Filed:
February 8, 2023
Publication date:
October 12, 2023
Inventors:
Douglas Wilson, Neil Bifulco, JR., Natasja Brooijmans, Joseph L. Kim, Emanuele Perola, Philip D. Ramsden, Richard Vargas, Steven Mark Wenglowsky
Abstract: or a stereoisomer or salt (e.g., pharmaceutically acceptable salt) thereof, wherein R1, R2, R3, R4, R5, p, m, and n are as defined herein. Use of the compounds as a component of a pharmaceutical compositions and methods for their use are also provided.
Type:
Application
Filed:
April 6, 2023
Publication date:
October 12, 2023
Inventors:
Hariprasad Vankayalapati, Zhaoliang Li, Kyle Medley, Kimberley Coffman, Dongqing Yan, David J. Bearss
Abstract: The invention provides compounds of Formula (I): as further described herein, as well as pharmaceutical compositions comprising such compounds, and methods to use the compounds and pharmaceutical compositions for treatment of certain viral disorders, including influenza.
Type:
Application
Filed:
February 27, 2023
Publication date:
October 12, 2023
Applicant:
Novartis AG
Inventors:
Maxime Dauphinais, Rama Jain, Dennis Christofer Koester, James R. Manning, Vanessa Marx, Daniel Poon, Lifeng Wan, Xiaojing Michael Wang, Aregahegn Yifru, Qian Zhao
Abstract: The present disclosure relates to processes for preparing (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide, solid state forms thereof, and corresponding pharmaceutical compositions, methods of treatment (including treatment of rheumatoid arthritis), kits, methods of synthesis, and products-by-process.
Type:
Application
Filed:
June 6, 2023
Publication date:
October 12, 2023
Inventors:
Ayman Allian, Jayanthy Jayanth, Mohamed-Eslam F. Mohamed, Mathew M. Mulhern, Fredrik Lars Nordstrom, Ahmed A. Othman, Michael J. Rozema, Lakshmi Bhagavatula, Patrick J. Marroum, Peter T. Mayer, Ahmad Y. Sheikh, Thomas B. Borchardt, Ben Klünder
Abstract: Highly porous nucleophilic organic cages (Nu-POC) were in-situ synthesized on cotton fibers by a condensation reaction between cyanuric chloride and melamine, and the products were employed as a robust wearable and flexible detoxifying protective material (denoted as POCotton) for vaporous pesticides. The covalent growth of Nu-POC particles on surfaces of cotton fibers retained the physical characteristics of Nu-POC to the greatest extend, which include specific surface area and porosity, while the cotton fabrics still remained wearable. The resultant POCotton can repeatedly adsorb fumigant vapors instantly (i.e., equilibrium reached within one minute) and massively (i.e., adsorption capacity at 596.88 mg/g of methyl iodide).
Abstract: Provided herein are solid forms comprising a compound of formula (I), or a stereoisomer, or a mixture of stereoisomers thereof, or a pharmaceutically acceptable salt thereof. Also provided herein are methods of synthesizing a compound of formula (I), pharmaceutical compositions comprising the same, and methods of treating, preventing, and managing various disorders using the compositions provided herein.
Type:
Application
Filed:
April 6, 2023
Publication date:
October 12, 2023
Inventors:
Christopher G. F. COOPER, Baudouin GERARD, Joshua Courtney HORAN, Jason T. KROPP, Benjamin Stephen LANE, David James PEARSON, Lauren Ashley MACEACHERN, Yameng HE, Mandeep SINGH, Arkesh NARAYANAPPA
Abstract: Disclosed herein are 1,2,3,4-tetrahydroisoquinolines and 4, 5, 6, 7-tetrahydrothieno [2, 3-cjpyridines, useful as antagonists of the muscarinic acetylcholine receptor M4 (mA·Ch·RM4). Also disclosed herein are methods of making the compounds, pharmaceutical compositions comprising the compounds, and methods of treating disorders using the compounds and compositions.
Type:
Application
Filed:
August 13, 2021
Publication date:
October 12, 2023
Inventors:
Aaron M. Bender, Matthew Spock, P. Jeffrey Conn, Craig W. Lindsley
Abstract: A light emitting device includes a first electrode, a second electrode facing the first electrode, and an emission layer disposed between the first electrode and the second electrode, wherein the emission layer includes a first compound represented by Formula 1 below:
Type:
Application
Filed:
February 24, 2023
Publication date:
October 12, 2023
Inventors:
Kyoung SUNWOO, TAEIL KIM, JUNHA PARK, MinJae SUNG, MUN-KI SIM, MINJUNG JUNG
Abstract: Disclosed are compounds of Formula (I) or a salt thereof, wherein Ring A is a carbon-linked ring; and Ring A, R1, and n are defined herein. Also disclosed are methods of using such compounds to inhibit Helios protein, and pharmaceutical compositions comprising such compounds. These compounds are useful in the treatment of viral infections and proliferative disorders, such as cancer.
Type:
Application
Filed:
March 22, 2021
Publication date:
October 12, 2023
Inventors:
Andrew P. Degnan, Godwin Kwame Kumi, Andrew J. Tebben, Audris Huang, Peter Kinam Park, Donna M. Bilder, Emily Charlotte Cherney, Ashok Vinayak Purandare
Abstract: The present invention concerns reagents for the reversible protection of biological molecules. It relates in particular to compounds derived from azaisatoic anhydride and their uses for the protection of biological molecules, particularly enzymes, in order to block their activity. The invention also relates to the biological molecules protected in this manner and to the methods for making use of these reagents.
Type:
Application
Filed:
June 2, 2023
Publication date:
October 12, 2023
Applicants:
BIOMÉRIEUX, UNIVERSITÉ DE CAEN NORMANDIE
Inventors:
Sylvain URSUEGUI, Alain LAURENT, Ali LAAYOUN, Frédéric FABIS
Abstract: The present invention relates to a pyrimidodiazepine derivative or a pharmaceutically acceptable salt thereof and a use thereof. A pyrimidodiazepine derivative or a pharmaceutically acceptable salt thereof according to the present invention can bind specifically to DNAJC3 and PDIA3, which are inhibitory of PERK signaling activation, to prevent the inhibition against PERK signaling. Thus, having an advantage of effectively suppressing or inhibiting tau aggregation, the pyrimidodiazepine derivative or a pharmaceutically acceptable salt thereof can not only be used in a pharmaceutical composition capable of fundamentally preventing or treating tauopathies associated with the activation of tau protein, but also can find applications in various studies on the development of therapeutic agents for tauopathies, and the expression or activity inhibition of tau protein.
Abstract: The present disclosure relates to certain chiral diaryl macrocyclic derivatives, pharmaceutical compositions containing them, and methods of using them to treat cancer.
Type:
Application
Filed:
March 17, 2023
Publication date:
October 12, 2023
Inventors:
Evan W. Rogers, Jane Ung, Vivian Nguyen, Dayong Zhai, Wei Deng, Jingrong J. Cui
Abstract: Described herein is a process for the preparation of a compound of Formula I, wherein R1 and R2 each have the meanings provided in the description. Also described is a process for the preparation of pharmaceutically-active compounds including the process for the preparation of compounds of Formula I.
Abstract: An object of the present invention is to provide a crystal of compound 1, which is useful as an antitumor agent, the crystal being stable, excellent in oral absorbability, highly chemically pure, and suitable for mass production. The present invention provides a crystal of compound 1 that exhibits an X-ray powder diffraction spectrum containing, at diffraction angles 2?±0.2°, characteristic peaks of at least 3 characteristic peaks selected from the group consisting of 5.8°, 9.8°, 12.2°, 14.0°, 15.3°, 21.1°, and 27.6°.
Abstract: Compounds and methods of using said compounds, singly or in combination with additional agents, and salts or pharmaceutical compositions of said compounds for the treatment of viral infections are disclosed.
Type:
Application
Filed:
March 1, 2023
Publication date:
October 12, 2023
Inventors:
Byoung-Kwon Chun, Rao V. Kalla, Richard L. Mackman
Abstract: The present invention relates to compounds of Formula I: wherein R1, L1, A, Xa, L2, B and Xb are each as defined herein. The present invention also relates to compounds of Formula II and III defined herein, formed by self-assembly of the compounds of Formula I with a metal M and an anion Q. Compounds of Formula II and III are useful in the treatment of proliferative disorders, such as cancer. The present invention also relates to pharmaceutical compositions comprising compounds of Formula I, II or III, and to the use of these compounds and compositions in the treatment of proliferative disorders, such as cancer.
Type:
Application
Filed:
August 10, 2021
Publication date:
October 12, 2023
Inventors:
Simon John Allison, Roger Mortimer Phillips, Craig Raymond Rice
Abstract: The present application relates to a pyrazole boronic acid compound represented by the following formula I, pharmaceutically acceptable salts or stereoisomers thereof, a pharmaceutical composition containing same, and uses thereof. The compound, the pharmaceutically acceptable salts or stereoisomers thereof and the pharmaceutical composition containing same can be used for preparing proteasome inhibitors.
Abstract: There is provided a silicon compound represented by General Formula (x). There is also provided a reactive material containing a silicon compound represented by General Formula (x).
Abstract: The present invention discloses photoinitiators according to the general formula R1R2R3—Ge—Ge—R4R5R6, wherein each R1 and R4 is an acyl group, and the use of such photoinitiators for radical polymerization.
Abstract: The present disclosure relates to a quinolinone derivative compound selectively binding to cysteine, an amino acid- or peptide-conjugate thereof, and an antibody-drug conjugate comprising same. Since a conjugate with high chemoselectivity and high yield is formed through a radical pathway induced by visible light, the present disclosure can be applied in various ways to bioconjugation.
Type:
Application
Filed:
August 25, 2021
Publication date:
October 12, 2023
Inventors:
Sungwoo HONG, Jaebong JANG, Hangyeol CHOI, Myojeong KIM
Abstract: The present invention provides aryl phosphorous oxide compounds with kinase inhibitory activity. The compounds are capable of effectively inhibiting activity of various types of EGFR drug-resistant mutants (such as EGFRdel19, EGFRdel19/T790M, EGFRdel19/C797S, EGFRT790M/L858R, EGFRL858/C797S, EGFRdel19/T790M/C797S, and EGFRL858R/T790M/C797S, and also have significant inhibitory effect on ALK fusion genes and mutants (such as L1196M), and are capable of being used for the treatment, combined treatment or prevention of various types of cancers.
Abstract: Various nucleoside phosphate and phosphonate analogues are provided for treatment of viral infections. Methods of preparing the analogues, pharmaceutical compositions containing the analogues, and methods of using the analogues as antiviral compounds, especially against adenoviruses, coronaviruses, and varicella zoster viruses, are also provided.
Abstract: The present invention relates to metal complexes and to electronic devices, in particular organic electroluminescent devices, containing these metal complexes.
Abstract: An organometallic compound represented by Formula 1, an organic light-emitting device including the organometallic compound, and a diagnostic composition including the organometallic compound: wherein, in Formula 1, Y2, a ring CY2, R1 to R8, R20, A1 to A7 and d2 may be each independently the same as described in the specification.
Type:
Application
Filed:
June 15, 2023
Publication date:
October 12, 2023
Inventors:
Yongsuk CHO, Soyeon KIM, Jiyoun LEE, Jongwon CHOI, Dmitry Kravchuk, Banglin LEE, Ohyun KWON, Kyuhyun IM
Abstract: An organometallic compound represented by Formula 1: M1(L1)n1(L2)n2??Formula 1 wherein, M1 is a transition metal, L1 is a ligand represented by Formula 1A, L2 is a ligand represented by Formula 1B, n1 and n2 are each independently 1 or 2, Formula 1A Formula 1B wherein X1 to X4 are each independently C or N, rings CY1 and ring CY2 are each independently a C5-C30 carbocyclic group or a C1-C30 heterocyclic group, Z1 and Z2 are each independently Si(Q1)(Q2)(Q3) or —Ge(Q1)(Q2)(Q3), provided that each of Z1 and Z2 is not —SiH3, a1 and a2 are each independently an integer from 0 to 10, a sum of a1 and a2 is 1 or greater, Y1 and Y2 are each independently O, S, Se, or C(R5)(R6), * and *? each indicates a binding site to M1, and R1 to R3, R5, R6, and R41 to R48 are as described herein.
Abstract: Cyclometalated iridium complexes having triphenylene or aza triphenylene and bulky alkyl substitution that can be used as emitters in OLEDs to improve the external quantum efficiency (EQE) and lifetime of OLEDs are disclosed.
Type:
Application
Filed:
June 2, 2023
Publication date:
October 12, 2023
Applicant:
UNIVERSAL DISPLAY CORPORATION
Inventors:
Zhiqiang JI, Alexey Borisovich DYATKIN, Jui-Yi TSAI, Pierre-Luc T. BOUDREAULT
Abstract: Novel ruthenium complexes of general formula 4 in which the substituents are defined herein. The present disclosure relates also to methods for preparing such compounds and use thereof as catalysts and/or (pre)catalysts in olefin cross metathesis.
Type:
Application
Filed:
August 17, 2021
Publication date:
October 12, 2023
Applicant:
Apeiron Synthesis S.A.
Inventors:
Rafal GAWIN, Andrzej Jan TRACZ, Patryk KRAJCZY
Abstract: Provided is a light-emitting device including an organometallic compound represented by Formula 1-1 or 1-2, an electronic apparatus including the light-emitting device, and the organometallic compound represented by Formula 1-1 or 1-2, wherein Formulae 1-1 and 1-2 are respectively the same as those described in the present specification.
Type:
Application
Filed:
November 2, 2022
Publication date:
October 12, 2023
Inventors:
Mina Jeon, Iljoon Kang, Sungbum Kim, Sujin Shin, Eunyoung Lee, Jinhee Ju
Abstract: Metal-assisted delayed fluorescent (MADF) emitters including cyclic tetradentate platinum (II) and palladium (II) complexes employing 8H-pyrido[3?,2?:4,5]-pyrrolo[3,2,1-de]acridine and its analogues. These complexes provide improved color purity and enhanced operational stability and are suitable for luminescent labels, emitters for organic light emitting diodes (OLEDs), and lighting applications.
Abstract: Disclosed are a device and a method for preparing a sucrose-6-ester. The device includes a tank body, a heating pipe, an annular cooling apparatus, and a motor, wherein the annular cooling device and the heating pipe are arranged in the tank body in nested manner; the annular cooling apparatus includes a condensation inner wall, a condenser pipe, and a condensation outer wall that are arranged in nested manner; a distillation chamber is formed between the heating pipe and the tank body, a condensation chamber is formed between the heating pipe and the condensation outer wall, and a hollow portion of the condensation inner wall forms a reaction chamber; the heating pipe and the condensation inner wall are drove by the motor to rotate; the heating pipe is provided with a vapor outlet; an evaporation residue channel is formed at an end of the heating pipe away from the feed inlet.
Abstract: Provided are stellate compounds that target spike proteins and have a significant anti-SARS-CoV-2 ability and a certain broad spectrum. Such molecules and salts thereof have at least one basic unit R(X)n, which binds at an orthotopic binding site such as an MD domain or an allosteric site, to a virus containing spike proteins or a virus having spike proteins on its surface, thereby preventing coronavirus or other viruses which express spike proteins on their surfaces from invading host cells, and preventing the occurrence of viral infection. In addition, interaction of the molecules and salts thereof with vitamin K-dependent proteins in the human body inhibits the expression of vitamin K so as to inhibit blood coagulation in the human body, thereby treating thrombosis caused by coronavirus and producing a curative effect for pneumonia caused by a severe viral infection.
Type:
Application
Filed:
May 24, 2023
Publication date:
October 12, 2023
Applicant:
SHENZHEN CELL INSPIRE PHARMACEUTICAL DEVELOPMENT CO., LTD.
Inventors:
Jun XU, Mengjiao HAO, Yuting ZHANG, Hao CHEN
Abstract: To extract, from plants such as freesia, a novel useful substance which is important in the food/pharmaceutical industry and which is expected to be useful for human health. The present inventors have found that an aromatic compound glycoside, which is a novel substance, is produced in a freesia cultivar having yellow petals such as “Ishikawa f2” in the flower thereof. The inventors have further confirmed that the glycoside exhibits an antioxidant effect, a lipid metabolism-improving effect, and a diabetes-ameliorating effect.
Abstract: [Problem] Provision of bridged nucleosides and nucleotides that are less susceptible to decomposition by nuclease in vivo, have high binding affinity and specificity for the target mRNA, and can efficiently regulate the expression of specific genes. [Solving Means] A compound represented by the following formula (I), a pharmaceutically acceptable salt thereof, or a pharmaceutically acceptable solvate thereof: in the formula (I), Base shows a purin-9-yl group or a 2-oxo-1,2-dihydropyrimidin-1-yl group optionally having one or more substituents, R1 and R2 are each independently a hydrogen atom or the like, and R3 and R4 are each independently a hydrogen atom or the like.
Abstract: The purpose of the present invention is to provide a stable composition comprising a nucleic acid oligomer having a phosphorothioate bond, and a process for preparing the same composition, and a process for preparing the nucleic acid oligomer efficiently from the composition. The present invention provides a composition comprising a nucleic acid oligomer having a phosphorothioate bond represented by formula (1) (wherein the symbols are defined in the specification), an alkylammonium salt, a water-soluble organic solvent, water, and an additive including at least one compound described in the specification. The present invention provides also a modified nucleic acid oligomer.
Abstract: The invention relates to a process for the production of a mixed P?O/P?S backbone oligonucleotide comprising a selective oxidation of an intermediary phosphite triester compound of formula I into a phosphodiester compound of formula II according to the scheme applying a novel oxidation protocol and to new oxidation solutions.
Abstract: The present invention refers to a process for preparing (3?,5?)-hydroxy-3-methyl-pregnan-20-one, a compound also known as Ganaxolone, having the formula below: (I):
Type:
Application
Filed:
September 8, 2021
Publication date:
October 12, 2023
Inventors:
Roberto Lenna, Andrea Fasana, Claudio Delfrate, Jerry David Ortiz Blacio
Abstract: Provided herein is a compound of Formula (I) or a pharmaceutically acceptable salt thereof, wherein R19, R5, R3a, R1a, R1b, R2a, R2b, R4a, R4b, R6a, R6b, R7a, R7b, R11a, R11b, R12a, R12b, R18, RD, and q are defined herein. L is selected from the group consisting of: wherein A indicates the point of attachment at C17 and wherein X is selected from the group consisting of —C(0)N(R55a)(R55b), —N(R55a)(R55b), —N(R55b)C(O)(R55a), and R55C wherein R55c is carbon-bound substituted or unsubstituted heteroaryl or substituted or unsubstituted aryl. Also provided herein are pharmaceutical compositions comprising a compound of Formula (I) and methods of using the compounds, e.g., in the treatment of CNS-related disorders.
Type:
Application
Filed:
December 5, 2019
Publication date:
October 12, 2023
Inventors:
Maria Jesus Blanco-Pillado, Francesco G. SALITURO, Marshall Lee MORNINGSTAR
Abstract: Provided herein is a compound of Formula (I) or a pharmaceutically acceptable salt thereof, wherein R19, R5, R3a, R1a, R1b, R2a, R2b, R4a, R4b, R6a, R6b, R7a, R7b, R11a, R11b, R12a, R12b, R18, RD, and q are defined herein. L is selected from the group consisting of: wherein A indicates the point of attachment at C17 and wherein X is selected from the group consisting of —C(O)N(R55a)(R55b) N(R55a)(R55b), —N(R55b)C(O)(R55a), and R55C wherein R55c is carbon-bound substituted or unsubstituted heteroaryl or substituted or unsubstituted aryl. Also provided herein are pharmaceutical compositions comprising a compound of Formula (I) and methods of using the compounds, e.g., in the treatment of CNS-related disorders.
Type:
Application
Filed:
June 13, 2023
Publication date:
October 12, 2023
Inventors:
Maria Jesus BLANCO-PILLADO, Francesco G. SALITURO, Marshall Lee MORNINGSTAR
Abstract: Provided herein is a compound of Formula (I) or a pharmaceutically acceptable salt thereof, wherein R19, R5, R3a, R1a, R1b, R2a, R2b, R4a, R4b, R6a, R6b, R7a, R7b, R11a, R11b, R12a, R12b, R18, RD, and q are defined herein. L is selected from the group consisting of: wherein A indicates the point of attachment at C17 and wherein X is selected from the group consisting of —C(O)N(R55a)(R55b), —N(R55a)(R55b), —N(R55b)C(O)(R55a), and R55C wherein R55c is carbon-bound substituted or unsubstituted heteroaryl or substituted or unsubstituted aryl. Also provided herein are pharmaceutical compositions comprising a compound of Formula (I) and methods of using the compounds, e.g., in the treatment of CNS-related disorders.
Type:
Application
Filed:
June 13, 2023
Publication date:
October 12, 2023
Inventors:
Maria Jesus BLANCO-PILLADO, Francesco G. SALITURO, Marshall Lee MORNINGSTAR
Abstract: Provided herein is a compound of Formula (I) or a pharmaceutically acceptable salt thereof, wherein R19, R5, R3a, R1a, R1b, R2a, R2b, R4a, R4b, R6a, R6b, R7a, R7b, R11a, R11b, R12a, R12b, R18, RD, and q are defined herein. L is selected from the group consisting of: wherein A indicates the point of attachment at C17 and wherein X is selected from the group consisting of —C(0)N(R55a)(R55b), —N(R55a)(R55b), —N(R55b)C(O)(R55a), and R55C wherein R55c is carbon-bound substituted or unsubstituted heteroaryl or substituted or unsubstituted aryl. Also provided herein are pharmaceutical compositions comprising a compound of Formula (I) and methods of using the compounds, e.g., in the treatment of CNS-related disorders.
Type:
Application
Filed:
June 13, 2023
Publication date:
October 12, 2023
Inventors:
Maria Jesus BLANCO-PILLADO, Francesco G. SALITURO, Marshall Lee MORNINGSTAR
Abstract: Disclosed herein are compounds (e.g., cancer) comprising a moiety that specifically binds to oligonucleotides comprising one or more repeats of GAAA (e.g., a pyrrole/imidazole polyamide) and bromodomain inhibitor and compositions and methods thereof for use in treating proliferative diseases and disorders.
Abstract: The invention provides an anti-allergic peptide and a use thereof for immune regulation and anti-allergy, the anti-allergic peptide is capable of inhibiting secretion of cytokines related to allergic reactions and regulating allergic reactions, and the anti-allergic peptide comprises an amino acid sequence shown in SEQ ID No: 1, SEQ ID No: 2, SEQ ID No: 3, SEQ ID No: 4 or SEQ ID No: 5, or a homologous amino acid sequence derived from substitution, deletion, and addition of one amino acid or more than one amino acid of any of the above sequences.
Type:
Application
Filed:
December 2, 2022
Publication date:
October 12, 2023
Inventors:
Pang Kuei HSU, Yu Cheng LIN, Chih Kuo KAO, Chia Feng WU
Abstract: The present invention relates to Regentide-012 and Regentide-013 and, more specifically, to a use of Regentide-012 and Regentide-013 for improving skin conditions. Regentide-012 and Regentide-013 according to the present invention is free of cytotoxicity and have remarkable effects of skin aging reduction, skin regeneration, skin elasticity improvement, skin wrinkle prevention, skin wrinkle reduction, and skin wound recovery and as such, can be variously utilized in the pharmaceutical, medicinal, cosmetic, and food fields.
Type:
Application
Filed:
June 8, 2021
Publication date:
October 12, 2023
Inventors:
Jae Hwan KIM, Ji Heon RHIM, Ri Ra LEE, Hye In AHN, Hae Yeong KANG, Ga Hyun KIM
Abstract: Provided herein are recombinantly engineered polypeptides capable of recycling noncanonical cofactors, and uses thereof. Further provided herein, is a universal growth selection process that can be used to identify said recombinantly engineered polypeptides.