Halogen substitution at the isoxazole ring enhances the activity of N-(isoxazolyl)sulfonamide endothelin antagonists-Reference-Cited by-同舟云学术

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Halogen substitution at the isoxazole ring enhances the activity of N-(isoxazolyl)sulfonamide endothelin antagonists

Published:1996-10 Issue:20 Volume:6 Page:2393-2398
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Ming Fai Chan ,Raju B.,Kois Adam,Castillo Rosario S.,Verner Erik J.,Chengde Wu ,Emily Hwang ,Okun Ilya,Stavros Fiona,Balaji V.N.

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference18 articles.

1. Presented in part at the 209th ACS National Meeting,1995

2. A novel potent vasoconstrictor peptide produced by vascular endothelial cells

3. Endothelin-3 is a novel neuropeptide: Isolation and sequence determination of endothelin-1 and endothelin-3 in porcine brain

4. Endothelin: a new challenge

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1. Synthesis, characterization, DFT, docking studies and molecular dynamics of some 3-phenyl-5-furan isoxazole derivatives as anti-inflammatory and anti-ulcer agents;Journal of Molecular Structure;2022-02

2. High-Throughput Screening and Drug Discovery;The Practice of Medicinal Chemistry;2008

3. DFT study of a novel lead structure in the isoxazole heterocyclic system;Journal of Molecular Structure: THEOCHEM;2003-09

4. Endothelin Receptor Antagonists;Endothelin and Its Inhibitors;2001

5. The discovery and structure—activity relationships of nonpeptide, low molecular weight antagonists selective for the endothelin ETB receptor;Bioorganic & Medicinal Chemistry;1998-12

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