N- versus C-Domain Selectivity of Catalytic Inactivation of Human Angiotensin Converting Enzyme by Lisinopril-Coupled Transition Metal Chelates-Reference-Cited by-同舟云学术

N- versus C-Domain Selectivity of Catalytic Inactivation of Human Angiotensin Converting Enzyme by Lisinopril-Coupled Transition Metal Chelates

Published:2013-12-05 Issue:24 Volume:56 Page:9826-9836
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Hocharoen Lalintip¹,Joyner Jeff C.¹²³,Cowan J. A.¹²³

Affiliation:

1. Evans Laboratory of Chemistry, The Ohio State University, 100 West 18th Avenue, Columbus, Ohio 43210, United States

2. The Ohio State Biochemistry Program, The Ohio State University, 784 Biological Sciences Building, 484 West 12th Avenue, Columbus, Ohio 43210, United States

3. MetalloPharm LLC, 1790 Riverstone Drive, Delaware, Ohio 43015, United States

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm4009345

Reference49 articles.

1. Angiotensin-Converting Enzyme Inhibitors

2. Skidgel, R. A.; Erdos, E.InThe Renin-Angiotensin System;Robertson, J. I. S.; Nicholls, M. G., Eds.Raven Press Ltd:New York, 1993; pp10.10–10.11.

3. Angiotensin-converting enzyme: new concepts concerning its biological role

4. The Comparative Effects of Angiotensin and Noradrenaline on Consecutive Vascular Sections

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