New Renin Inhibitors Containing Pseudodipeptidic Units in P3-P2 and P1-P1' Positions
Author:
Affiliation:
1. Department of Drug Chemistry, Medical University, Poland
2. National Institute of Public Health, Poland
Publisher
Pharmaceutical Society of Japan
Subject
Drug Discovery,General Chemistry,General Medicine
Link
http://www.jstage.jst.go.jp/article/cpb/53/10/53_10_1305/_pdf
Reference22 articles.
1. Computer graphics modelling of human renin
2. Nonpeptide Renin Inhibitors with Good Intraduodenal Bioavailability and Efficacy in Dog
3. Structure-based drug design: the discovery of novel nonpeptide orally active inhibitors of human renin
4. Rational design, synthesis, and X-ray structure of renin inhibitors with extended P1 sidechains
5. Bioactive hydroxyethylene dipeptide isosteres with hydrophobic (P3-P1)-moieties. A novel strategy towards small non-peptide renin inhibitors
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1. Synthesis and docking studies of renin inhibitors containing ester and amide derivatives of (3S, 4S)-4-amino-hydroxy acids with S3-S3’ renin binding site.;Acta Poloniae Pharmaceutica - Drug Research;2021-04-07
2. Novel renin inhibitors containing derivatives of N-alkylleucyl-β -hydroxy-γ -amino acids;Journal of Peptide Science;2016-01-19
3. Novel renin inhibitors containing a non-peptide aminoalkanoyl moiety at P-1-P-1 ' position;PHARMAZIE;2014
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