Halogen substitution at the isoxazole ring enhances the activity of N-(isoxazolyl)sulfonamide endothelin antagonists
- 22 October 1996
- journal article
- Published by Elsevier in Bioorganic & Medicinal Chemistry Letters
- Vol. 6 (20) , 2393-2398
- https://doi.org/10.1016/0960-894x(96)00441-6
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- Chapter 10. Progress in the Development of Endothelin Receptor AntagonistsPublished by Elsevier ,1995
- Identification of a New Class of ETA Selective Endothelin Antagonists by Pharmacophore Directed ScreeningBiochemical and Biophysical Research Communications, 1994
- Chapter 7. Small Molecule Endothelin Receptor AntagonistsPublished by Elsevier ,1994
- Endothelin: a new challengeJournal of Medicinal Chemistry, 1992
- Chapter 9. Endogenous Vasoactive PeptidesPublished by Elsevier ,1992
- Chapter 9. Endogenous Vasoactive PeptidesPublished by Elsevier ,1991
- Cloning of a cDNA encoding a non-isopeptide-selective subtype of the endothelin receptorNature, 1990
- Cloning and expression of a cDNA encoding an endothelin receptorNature, 1990
- Endothelin-3 is a novel neuropeptide: Isolation and sequence determination of endothelin-1 and endothelin-3 in porcine brainBiochemical and Biophysical Research Communications, 1989
- A novel potent vasoconstrictor peptide produced by vascular endothelial cellsNature, 1988