Design and Synthesis of New Linear and Cyclic Bradykinin Antagonists
- 1 January 1996
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of Medicinal Chemistry
- Vol. 39 (10) , 2095-2101
- https://doi.org/10.1021/jm950682e
Abstract
No abstract availableKeywords
This publication has 19 references indexed in Scilit:
- New cyclic bradykinin antagonists containing disulfide and lactam bridges at the N‐terminal sequence*International Journal of Peptide and Protein Research, 1995
- p-Guanidinobenzoyl-[Hyp3, Thi5, D-Tic7, Oic8]bradykinin is almost completely devoid of the agonist effect of HOE140 on the endothelium-free femoral artery of sheep.Bioorganic & Medicinal Chemistry Letters, 1994
- Allyl‐based groups for side‐chain protection of amino‐acidsInternational Journal of Peptide and Protein Research, 1993
- Design of potent, cyclic peptide bradykinin receptor antagonists from conformationally constrained linear peptidesJournal of Medicinal Chemistry, 1993
- Constrained phenylalanine analoguesInternational Journal of Peptide and Protein Research, 1992
- Photochemistry of 4-substituted (phenylethynyl)triphenyl borate salts: analysis of the visible-region electronic absorption spectra of tetraarylboratirene anionsThe Journal of Organic Chemistry, 1992
- Induction of vascular smooth muscle bradykinin B1 receptorsin vivo during antigen arthritisInflammation Research, 1991
- Validation of the general purpose tripos 5.2 force fieldJournal of Computational Chemistry, 1989
- Kinin Formation: Mechanisms and Role in Inflammatory DisordersAnnual Review of Immunology, 1988
- pA2 and receptor differentiation: A statistical analysis of competitive antagonismLife Sciences, 1979