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Showing results (21-30 of 29) with videos related to

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Journal of the American Chemical Society|October 3, 2002
Substrate-based design of the first class of angiotensin-converting enzyme-related carboxypeptidase (ACE2) inhibitorsNatalie A Dales, Alexandra E Gould, James A Brown, et al.
Bioorganic & Medicinal Chemistry Letters|June 19, 2004
Synthesis and biological evaluation of imidazole-based small molecule antagonists of the melanocortin 4 receptor (MC4-R)Thomas H Marsilje, Jonathan B Roses, Emily F Calderwood, et al.
Journal of Medicinal Chemistry|October 18, 2011
Antibacterial optimization of 4-aminothiazolyl analogues of the natural product GE2270 A: identification of the cycloalkylcarboxylic acidsMatthew J LaMarche, Jennifer A Leeds, Kerri Amaral, et al.
Journal of Medicinal Chemistry|March 19, 2004
Identification of 2-[2-[2-(5-bromo-2- methoxyphenyl)-ethyl]-3-fluorophenyl]-4,5-dihydro-1H-imidazole (ML00253764), a small molecule melanocortin 4 receptor antagonist that effectively reduces tumor-induced weight loss in a mouse modelTricia J Vos, Andrei Caracoti, Jennifer L Che, et al.
Journal of Medicinal Chemistry|June 30, 2016
Antibacterial and Solubility Optimization of Thiomuracin AMatthew J LaMarche, Jennifer A Leeds, Jason Brewer, et al.
Antimicrobial Agents and Chemotherapy|August 10, 2011
In vitro and in vivo activities of novel, semisynthetic thiopeptide inhibitors of bacterial elongation factor TuJ A Leeds, M J LaMarche, J T Brewer, et al.
Bioorganic & Medicinal Chemistry Letters|August 9, 2005
Identification of ortho-amino benzamides and nicotinamides as MCHr1 antagonistsAnil Vasudevan, Matthew J LaMarche, Christopher Blackburn, et al.
Journal of Medicinal Chemistry|February 10, 2012
Discovery of LFF571: an investigational agent for Clostridium difficile infectionMatthew J LaMarche, Jennifer A Leeds, Adam Amaral, et al.
Nature|May 18, 2018
Author Correction: Discovery of a selective catalytic p300/CBP inhibitor that targets lineage-specific tumoursLoren M Lasko, Clarissa G Jakob, Rohinton P Edalji, et al.
Pageof 3

Showing results (21-30 of 29) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 29 results.
Journal of the American Chemical Society|October 3, 2002
Substrate-based design of the first class of angiotensin-converting enzyme-related carboxypeptidase (ACE2) inhibitorsNatalie A Dales, Alexandra E Gould, James A Brown, et al.
Bioorganic & Medicinal Chemistry Letters|June 19, 2004
Synthesis and biological evaluation of imidazole-based small molecule antagonists of the melanocortin 4 receptor (MC4-R)Thomas H Marsilje, Jonathan B Roses, Emily F Calderwood, et al.
Journal of Medicinal Chemistry|October 18, 2011
Antibacterial optimization of 4-aminothiazolyl analogues of the natural product GE2270 A: identification of the cycloalkylcarboxylic acidsMatthew J LaMarche, Jennifer A Leeds, Kerri Amaral, et al.
Journal of Medicinal Chemistry|March 19, 2004
Identification of 2-[2-[2-(5-bromo-2- methoxyphenyl)-ethyl]-3-fluorophenyl]-4,5-dihydro-1H-imidazole (ML00253764), a small molecule melanocortin 4 receptor antagonist that effectively reduces tumor-induced weight loss in a mouse modelTricia J Vos, Andrei Caracoti, Jennifer L Che, et al.
Journal of Medicinal Chemistry|June 30, 2016
Antibacterial and Solubility Optimization of Thiomuracin AMatthew J LaMarche, Jennifer A Leeds, Jason Brewer, et al.
Antimicrobial Agents and Chemotherapy|August 10, 2011
In vitro and in vivo activities of novel, semisynthetic thiopeptide inhibitors of bacterial elongation factor TuJ A Leeds, M J LaMarche, J T Brewer, et al.
Bioorganic & Medicinal Chemistry Letters|August 9, 2005
Identification of ortho-amino benzamides and nicotinamides as MCHr1 antagonistsAnil Vasudevan, Matthew J LaMarche, Christopher Blackburn, et al.
Journal of Medicinal Chemistry|February 10, 2012
Discovery of LFF571: an investigational agent for Clostridium difficile infectionMatthew J LaMarche, Jennifer A Leeds, Adam Amaral, et al.
Nature|May 18, 2018
Author Correction: Discovery of a selective catalytic p300/CBP inhibitor that targets lineage-specific tumoursLoren M Lasko, Clarissa G Jakob, Rohinton P Edalji, et al.
Pageof 3