New Bradykinin Analogues Modified in the C-Terminal Part with Sterically Restricted 1-Aminocyclohexane-1-carboxylic Acid-Reference-Cited by-同舟云学术

New Bradykinin Analogues Modified in the C-Terminal Part with Sterically Restricted 1-Aminocyclohexane-1-carboxylic Acid

Published:2005-11-16 Issue:25 Volume:48 Page:8055-8059
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Labudda-Dawidowska Olga¹,Wierzba Tomasz H.¹,Prahl Adam¹,Kowalczyk Wioleta¹,Gawiński Łukasz¹,Plackova Marketa¹,Slaninová Jiřina¹,Lammek Bernard¹

Affiliation:

1. Faculty of Chemistry, University of Gdańsk, Sobieskiego 18, 80-952 Gdańsk, Poland, Department of Physiology, Medical University of Gdańsk, Dȩbinki 1, 80-211 Gdańsk, Poland, and Group of Peptide Biochemistry, Institute of Organic Chemistry and Biochemistry, Academy of Sciences of Czech Republic, Flemingovo Sq.2, Prague 6, CZ-16610, Czech Republic

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm0580353

Reference27 articles.

1. Bradykinin Antagonists

2. Bradyzide, a potent non-peptide B2bradykinin receptor antagonist with long-lasting oral activity in animal models of inflammatory hyperalgesia

3. Biochemical and Molecular Pharmacology of Kinin Receptors

4. Expression cloning of a human B1 bradykinin receptor.

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