Zobrazeno 1 - 10
of 70
pro vyhledávání: '"John R. Proudfoot"'
Autor:
Steven J. Taylor, Asitha Abeywardane, Shuang Liang, Zhaoming Xiong, John R. Proudfoot, Bennett Sandy Farmer, Donghong A. Gao, Alexander Heim-Riether, Lana Louise Smith-Keenan, Ingo Muegge, Yang Yu, Qiang Zhang, Donald Souza, Mark Panzenbeck, Daniel Goldberg, Melissa Hill-Drzewi, Mariana Margarit, Brandon Collins, John Xiang Li, Ljiljana Zuvela-Jelaska, Jun Li, Neil A. Farrow
Publikováno v:
ACS Omega, Vol 6, Iss 29, Pp 18635-18650 (2021)
Externí odkaz:
https://doaj.org/article/28925716e0524cb7af79c7a4126b692b
Autor:
Huaping Zhang, Marta K. Dudek, John R. Proudfoot, Michał Gleńsk, Victor W. Day, Jan A. Gliński, Izabela D. Madura
Publikováno v:
Journal of Natural Products. 82:3477-3481
Prolonged storage of technical abamectin as well as avermectin B1a samples yielded a previously unknown derivative, designated here as compound 1. Detailed NMR analysis and X-ray crystallography allowed us to determine the structure of this compound
Autor:
John Xiang Li, Steven John Taylor, Mariana Margarit, Jun Li, Yu Yang, Qiang Zhang, Ingo Muegge, Melissa Hill-Drzewi, Alexander Heim-Riether, Mark Panzenbeck, Asitha Abeywardane, Zhaoming Xiong, Daniel R. Goldberg, Bennett Sandy Farmer, Gao Donghong A, Ljiljana Zuvela-Jelaska, John R. Proudfoot, Shuang Liang, Donald Souza, Lana Louise Smith-Keenan, Neil A. Farrow, Brandon Collins
Publikováno v:
ACS Omega
ACS Omega, Vol 6, Iss 29, Pp 18635-18650 (2021)
ACS Omega, Vol 6, Iss 29, Pp 18635-18650 (2021)
Here, we described the design, by fragment merging and multiparameter optimization, of selective MMP-13 inhibitors that display an appropriate balance of potency and physicochemical properties to qualify as tool compounds suitable for in vivo testing
Autor:
Florian Grebien, Abootaleb Sedighi, Roman Wolfgang Fleck, Siawash Ahmar, Kay Noel, Mulu Geletu, Ji Sung Park, Elizabeth Heyes, Mohammad S. Eram, Elvin D. de Araujo, Angel Sampedro, Patrick T. Gunning, Helena Sorger, Gary Tin, Dziyana Kraskouskaya, Ruth Villalonga, Marco Herling, Jeff A O'Meara, John R. Proudfoot, Anna Orlova, Richard Moriggl, Satu Mustjoki
Publikováno v:
Cancer Research. 80:LB-108
STAT5 is a member of the signal transducer and activator of transcription family of proteins and is widely recognized as an oncogenic master regulator of hematological malignancies. To date, therapeutic approaches to attenuate aberrant activity have
Autor:
John R. Proudfoot
Publikováno v:
The Journal of organic chemistry. 82(13)
An atom-environment complexity measure, CA, to assess local changes in complexity during synthetic transformations is described. The complexity measure is based on applying Shannon’s equation to the number and diversity of paths up to two bonds in
Autor:
John R. Proudfoot
Publikováno v:
Bioorganicmedicinal chemistry letters. 27(9)
An atom environment, path based approach to calculating molecular complexity is described. Based on Shannon's equation, the method transforms the number and diversity of paths emanating from an atom to an atom-complexity from which a number of molecu
Autor:
Paul W. Erhardt, Joerg Senn-Bilfinger, Derek R. Buckle, C. Robin Ganellin, Toshi Kobayashi, John R. Proudfoot, Thomas J. Perun
Publikováno v:
Pure and Applied Chemistry. 85:1725-1758
The evolution that has taken place in medicinal chemistry practice as a result of major advances in genomics and molecular biology arising from the Human Genome Project has carried with it an extensive additional working vocabulary that has become bo
Autor:
Xiang Li, Hidenori Takahashi, Steven S. Pullen, Stéphane De Lombaert, Asitha Abeywardane, Ming-Hong Hao, John R. Proudfoot, Anil Kumar Padyana, Brandon Collins, Leslie Martin, Daniel R. Albaugh, Steven John Taylor, Shuang Liang, Bennett Sandy Farmer, Melissa Hill-Drzewi
Publikováno v:
Journal of Medicinal Chemistry. 56:4465-4481
Chymase plays an important and diverse role in the homeostasis of a number of cardiovascular processes. Herein, we describe the identification of potent, selective chymase inhibitors, developed using fragment-based, structure-guided linking and optim
Autor:
Dominique Besson, Jan E. Blanchard, Robert P. Hertzberg, Pascal Villa, John R. Proudfoot, Richard R. Neubig, Lyndon E. Llewellyn, Denis J. Crankshaw, Carol Ann Homon, John Wang, Larry A. Walker, Olivier Nosjean, Günter Gauglitz
Publikováno v:
Pure and Applied Chemistry. 83:1129-1158
Biomolecular screening is now a crucial component of the drug discovery process, and this glossary will be of use to practitioners in the field of screening and to those who interact with the screening community. The glossary contains definitions rel
Autor:
Alison Kukulka, Ho Yin Lo, Roman Wolfgang Fleck, Raj Betageri, Mary Ann Hoermann, Usha R. Patel, Stéphane De Lombaert, Alisa K. Kabcenell, Richard H. Ingraham, Rajiv Sharma, Kirrane Thomas M, John R. Proudfoot, Neil A. Farrow, Chuk Chui Man
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 20:6379-6383
A novel series of pyrazole sEH inhibitors is reported. Lead optimization efforts to replace the aniline core are also described. In particular, 2-pyridine, 3-pyridine and pyridazine analogs are potent sEH inhibitors with favorable CYP3A4 inhibitory a