Rational design, synthesis and pharmacological characterization of novel aminopeptidase A inhibitors-Reference-Cited by-同舟云学术

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Rational design, synthesis and pharmacological characterization of novel aminopeptidase A inhibitors

Published:2024-11 Issue: Volume:113 Page:129940
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Balavoine Fabrice,Compere Delphine,Miege Frédéric,De Mota Nadia,Keck Mathilde,Fer Mickael,Christen Aude,Martin Emmeline,Roche Didier,Llorens-Cortes Catherine,Rodeschini Vincent

Funder

Institut National de la Santé et de la Recherche Médicale

Fondation du Collège de France

Agence Nationale de la Recherche

Publisher

Elsevier BV

Reference35 articles.

1. A mammalian peptidase specific for the hydrolysis of N-terminal α-L-glutamyl and aspartyl residues;Glenner;Nature,1962

2. Purification of aminopeptidase A in human serum and degradation of angiotensin II by the purified enzyme;Nagatsu;BBA,1970

3. Identification of metabolic pathways of brain angiotensin II and III using specific aminopeptidase inhibitors: predominant role of angiotensin III in the control of vasopressin release;Zini;PNAS,1996

4. The in vivo metabolism of cholecystokinin (CCK-8) is essentially ensured by aminopeptidase A;Migaud;Peptides,1996

5. Families of zinc metalloproteases;Hooper;FEBS Lett,1994

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