Controlled Modification of Acidity in Cholecystokinin B Receptor Antagonists: N-(1,4-Benzodiazepin-3-yl)-N ‘-[3-(tetrazol-5-ylamino)phenyl]ureas-Reference-Cited by-同舟云学术

Controlled Modification of Acidity in Cholecystokinin B Receptor Antagonists: N-(1,4-Benzodiazepin-3-yl)-N ‘-[3-(tetrazol-5-ylamino)phenyl]ureas

Published:1996-01-01 Issue:4 Volume:39 Page:842-849
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Castro José L.¹,Ball Richard G.¹,Broughton Howard B.¹,Russell Michael G. N.¹,Rathbone Denise¹,Watt Alan P.¹,Baker Raymond¹,Chapman Kerry L.¹,Fletcher Alan E.¹,Patel Smita¹,Smith Alison J.¹,Marshall George R.¹,Ryecroft Wayne¹,Matassa Victor G.¹

Affiliation:

1. Chemistry, Biochemistry, and Pharmacology Departments, Merck Sharp & Dohme Research Laboratories, Neuroscience Research Centre, Terlings Park, Eastwick Road, Harlow, Essex CM20 2QR, U.K., and Biophysical Chemistry Department, Merck Research Laboratories, Rahway, New Jersey 07065

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm9506736

Reference53 articles.

1. Molecular Cloning, Functional Expression and Chromosomal Localization of the Human Cholecystokinin Type A Receptor

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