Metal Coordination-Based Inhibitors of Adenylyl Cyclase: Novel Potent P-Site Antagonists
Author:
Affiliation:
1. Departments of Medicinal Chemistry and Biology, Millennium Pharmaceuticals, Inc., 256 East Grand Avenue, South San Francisco, California 94080
Publisher
American Chemical Society (ACS)
Subject
Drug Discovery,Molecular Medicine
Link
https://pubs.acs.org/doi/pdf/10.1021/jm0205604
Reference22 articles.
1. Forskolin Derivatives with Increased Selectivity for Cardiac Adenylyl Cyclase
2. Adenylyl cyclase types I and VI but not II and V are selectively inhibited by nitric oxide
3. Reprinted fromBioorg. Med. Chem. Lett., Vol. 12, Levy, D. E.; Marlowe, C.; Kane-Maguire, K.; Bao, M.; Cherbavaz, D. B.; Tomlinson, J. E.; Sedlock, D. M.; Scarborough, R. M. Hydroxamate based inhibitors of adenylyl cyclase. Part 1: The effect of acyclic linkers on P-site binding, pp 3085−3088, Copyright 2002, with permission from Elsevier Science.
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