Zobrazeno 1 - 10
of 176
pro vyhledávání: '"Malcolm, Maccoss"'
Autor:
Alastair D. G. Lawson, Malcolm MacCoss, Dominique L. Baeten, Alex Macpherson, Jiye Shi, Alistair J. Henry
Publikováno v:
Frontiers in Chemistry, Vol 9 (2021)
Over the last 10 years considerable progress has been made in the application of small molecules to modulating protein-protein interactions (PPIs), and the navigation from “undruggable” to a host of candidate molecules in clinical trials has been
Externí odkaz:
https://doaj.org/article/55d3049b08ac473c93e38790581f0e57
Autor:
Martin A. Lowe, Alvaro Cardenas, Jean-Pierre Valentin, Zhaoning Zhu, Jan Abendroth, Jose L. Castro, Reiner Class, Annie Delaunois, Renaud Fleurance, Helga Gerets, Vitalina Gryshkova, Lloyd King, Donald D. Lorimer, Malcolm MacCoss, Julian H. Rowley, Marie-Luce Rosseels, Leandro Royer, Richard D. Taylor, Melanie Wong, Oliver Zaccheo, Vishal P. Chavan, Gokul A. Ghule, Bapusaheb K. Tapkir, Jeremy N. Burrows, Maëlle Duffey, Matthias Rottmann, Sergio Wittlin, Iñigo Angulo-Barturen, María Belén Jiménez-Díaz, Josefine Striepen, Kate J. Fairhurst, Tomas Yeo, David A. Fidock, Alan F. Cowman, Paola Favuzza, Benigno Crespo-Fernandez, Francisco Javier Gamo, Daniel E. Goldberg, Dominique Soldati-Favre, Benoît Laleu, Teresa de Haro
Publikováno v:
Journal of Medicinal Chemistry. 65:14121-14143
Publikováno v:
Journal of medicinal chemistry. 65(13)
We present a comprehensive analysis of all ring systems (both heterocyclic and nonheterocyclic) in clinical trial compounds and FDA-approved drugs. We show 67% of small molecules in clinical trials comprise only ring systems found in marketed drugs,
Autor:
Alistair James Henry, Malcolm MacCoss, Dominique Baeten, Jiye Shi, Alex Macpherson, Alastair D. G. Lawson
Publikováno v:
Frontiers in Chemistry, Vol 9 (2021)
Frontiers in chemistry, 9:668186. Frontiers Media S.A.
Frontiers in Chemistry
Frontiers in chemistry, 9:668186. Frontiers Media S.A.
Frontiers in Chemistry
Over the last 10 years considerable progress has been made in the application of small molecules to modulating protein-protein interactions (PPIs), and the navigation from “undruggable” to a host of candidate molecules in clinical trials has been
Publikováno v:
Journal of Medicinal Chemistry. 61:4283-4289
Tackling PPIs, particularly by stabilizing clinically favored conformations of target proteins, with orally available, bona fide small molecules remains a significant but immensely worthwhile challenge for the pharmaceutical industry. Success may be
Autor:
Timothy W. Gorman, Benedicte Lallemand, Malcolm MacCoss, Michael C. Willis, Christopher J. Schofield, José L. Castro, Alistair J. M. Farley, Darren J. Dixon, Martin D. Smith, Bryony L. Elbert, Tarn C. Johnson, Jakub Flasz, Christophe Genicot, Robert S. Paton, Patrick Pasau
Publikováno v:
Chemical Science. 9(3)
Sulfones feature prominently in biologically active molecules and are key functional groups for organic synthesis. We report a mild, photoredox-catalyzed reaction for sulfonylation of aniline derivatives with sulfinate salts, and demonstrate the util
Publikováno v:
Journal of medicinal chemistry. 61(10)
Tackling PPIs, particularly by stabilizing clinically favored conformations of target proteins, with orally available, bona fide small molecules remains a significant but immensely worthwhile challenge for the pharmaceutical industry. Success may be
Publikováno v:
Journal of Medicinal Chemistry. 57:5845-5859
We have analyzed the rings, ring systems, and frameworks in drugs listed in the FDA Orange Book to understand the frequency, timelines, molecular property space, and the application of these rings in different therapeutic areas and target classes. Th
Publikováno v:
Journal of medicinal chemistry. 60(5)
We have enumerated all linear combinations of ring systems from FDA approved drugs, up to three rings in length and up to four bonds linkers to give an in silico database of approximately 14 million molecules. This virtual library was compared with m
Autor:
Jeremy Clark, Xiao Tong, Ashok Arasappan, Randall R. Rossman, Anita T. Fowler, Subramaniam Ananthan, Vinay Girijavallabhan, Feng Geng, Regina Huelgas, Neng-Yang Shih, F. George Njoroge, Hollis S. Kezar, Joseph A. Maddry, Yuhua Huang, Frank Bennett, Cheng Li, John J. Piwinski, Cecil D. Kwong, John A. Secrist, Stephanie Curry, Abhijit Roychowdhury, Malcolm MacCoss, Robert C. Reynolds, Hsueh-Cheng Huang, Robert Chase
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 22:5144-5149
Introduction of nitrogen atom into the benzene ring of a previously identified HCV replication (replicase) benzofuran inhibitor 2, resulted in the discovery of the more potent pyridofuran analogue 5. Subsequent introduction of small alkyl and alkoxy