The Most Potent Organophosphorus Inhibitors of Leucine Aminopeptidase. Structure-Based Design, Chemistry, and Activity-Reference-Cited by-同舟云学术

The Most Potent Organophosphorus Inhibitors of Leucine Aminopeptidase. Structure-Based Design, Chemistry, and Activity

Published:2003-05-20 Issue:13 Volume:46 Page:2641-2655
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Grembecka Jolanta¹,Mucha Artur¹,Cierpicki Tomasz¹,Kafarski Paweł¹

Affiliation:

1. Institute of Organic Chemistry, Biochemistry and Biotechnology, Wrocław University of Technology, Wybrzeże Wyspiańskiego 27, 50−370 Wrocław, and Institute of Biochemistry and Molecular Biology, University of Wrocław, Tamka 2, 50−137 Wrocław, Poland

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm030795v

Reference89 articles.

1. INHIBITORS OF HIV-1 PROTEASE: A Major Success of Structure-Assisted Drug Design

2. Structure-based drug design

3. STRUCTURE-BASED DRUG DESIGN:Computational Advances

4. Aminopeptidases: structure and function

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