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Journal of Medicinal Chemistry
|
January 30, 2016
Discovery of a Potent Class I Protein Arginine Methyltransferase Fragment Inhibitor
Renato Ferreira de Freitas, Mohammad S Eram, Magdalena M Szewczyk, et al.
Biorxiv : the Preprint Server for Biology
|
February 23, 2021
Probing the SAM Binding Site of SARS-CoV-2 nsp14 in vitro Using SAM Competitive Inhibitors Guides Developing Selective bi-substrate Inhibitors
Kanchan Devkota, Matthieu Schapira, Sumera Perveen, et al.
Nature Communications
|
April 25, 2019
A chemical toolbox for the study of bromodomains and epigenetic signaling
Qin Wu, David Heidenreich, Stanley Zhou, et al.
Chemmedchem
|
June 24, 2021
Development of LM98, a Small-Molecule TEAD Inhibitor Derived from Flufenamic Acid
Léa Mélin, Shuay Abdullayev, Ahmed Fnaiche, et al.
SLAS Discovery : Advancing Life Sciences R & D
|
March 23, 2018
Discovery of Small-Molecule Antagonists of the H3K9me3 Binding to UHRF1 Tandem Tudor Domain
Guillermo Senisterra, Hugh Y Zhu, Xiao Luo, et al.
SLAS Discovery : Advancing Life Sciences R & D
|
July 1, 2021
Probing the SAM Binding Site of SARS-CoV-2 Nsp14 In Vitro Using SAM Competitive Inhibitors Guides Developing Selective Bisubstrate Inhibitors
Kanchan Devkota, Matthieu Schapira, Sumera Perveen, et al.
ACS Medicinal Chemistry Letters
|
July 24, 2018
LLY-283, a Potent and Selective Inhibitor of Arginine Methyltransferase 5, PRMT5, with Antitumor Activity
Zahid Q Bonday, Guillermo S Cortez, Michael J Grogan, et al.
ACS Chemical Biology
|
November 25, 2015
A Potent, Selective, and Cell-Active Inhibitor of Human Type I Protein Arginine Methyltransferases
Mohammad S Eram, Yudao Shen, Magdalena Szewczyk, et al.
European Journal of Medicinal Chemistry
|
March 8, 2026
Identification and optimization of first-in-class RNA helicase inhibitors of DDX1, LGP2, and MDA5
Xiaowen Wang, Feijun Wang, Deyu Kong, et al.
SLAS Discovery : Advancing Life Sciences R & D
|
October 22, 2022
Discovery of hit compounds for methyl-lysine reader proteins from a target class DNA-encoded library
Devan J Shell, Justin M Rectenwald, Peter H Buttery, et al.
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Search research articles
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Showing results (191-200 of 253) with videos related to
Sort By:
Page
of 26
Journal of Medicinal Chemistry
|
January 30, 2016
Discovery of a Potent Class I Protein Arginine Methyltransferase Fragment Inhibitor
Renato Ferreira de Freitas, Mohammad S Eram, Magdalena M Szewczyk, et al.
Biorxiv : the Preprint Server for Biology
|
February 23, 2021
Probing the SAM Binding Site of SARS-CoV-2 nsp14 in vitro Using SAM Competitive Inhibitors Guides Developing Selective bi-substrate Inhibitors
Kanchan Devkota, Matthieu Schapira, Sumera Perveen, et al.
Nature Communications
|
April 25, 2019
A chemical toolbox for the study of bromodomains and epigenetic signaling
Qin Wu, David Heidenreich, Stanley Zhou, et al.
Chemmedchem
|
June 24, 2021
Development of LM98, a Small-Molecule TEAD Inhibitor Derived from Flufenamic Acid
Léa Mélin, Shuay Abdullayev, Ahmed Fnaiche, et al.
SLAS Discovery : Advancing Life Sciences R & D
|
March 23, 2018
Discovery of Small-Molecule Antagonists of the H3K9me3 Binding to UHRF1 Tandem Tudor Domain
Guillermo Senisterra, Hugh Y Zhu, Xiao Luo, et al.
SLAS Discovery : Advancing Life Sciences R & D
|
July 1, 2021
Probing the SAM Binding Site of SARS-CoV-2 Nsp14 In Vitro Using SAM Competitive Inhibitors Guides Developing Selective Bisubstrate Inhibitors
Kanchan Devkota, Matthieu Schapira, Sumera Perveen, et al.
ACS Medicinal Chemistry Letters
|
July 24, 2018
LLY-283, a Potent and Selective Inhibitor of Arginine Methyltransferase 5, PRMT5, with Antitumor Activity
Zahid Q Bonday, Guillermo S Cortez, Michael J Grogan, et al.
ACS Chemical Biology
|
November 25, 2015
A Potent, Selective, and Cell-Active Inhibitor of Human Type I Protein Arginine Methyltransferases
Mohammad S Eram, Yudao Shen, Magdalena Szewczyk, et al.
European Journal of Medicinal Chemistry
|
March 8, 2026
Identification and optimization of first-in-class RNA helicase inhibitors of DDX1, LGP2, and MDA5
Xiaowen Wang, Feijun Wang, Deyu Kong, et al.
SLAS Discovery : Advancing Life Sciences R & D
|
October 22, 2022
Discovery of hit compounds for methyl-lysine reader proteins from a target class DNA-encoded library
Devan J Shell, Justin M Rectenwald, Peter H Buttery, et al.
Page
of 26