Pentafluorosulfanyl-Substituted Benzopyran Analogues As New Cyclooxygenase-2 Inhibitors with Excellent Pharmacokinetics and Efficacy in Blocking Inflammation
Author:
Affiliation:
1. Drug Discovery Pipeline, Guangzhou Institutes of Biomedicine and Health, 190 Kaiyuan Avenue, Science City, Guangzhou 510530, P.R. China
2. Euclises Pharmaceuticals, St. Louis, Missouri 63108, United States
Funder
Guangdong Science and Technology Department
Guangzhou Science and Technology Program key projects
Chinese Academy of Sciences
Publisher
American Chemical Society (ACS)
Subject
Drug Discovery,Molecular Medicine
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.jmedchem.6b01484
Reference68 articles.
1. Synthesis of Deuterated Benzopyran Derivatives as Selective COX-2 Inhibitors with Improved Pharmacokinetic Properties
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3. Synthetic chemistry and biological activity of pentafluorosulphanyl (SF5) organic molecules
4. The synthesis and biological activity of pentafluorosulfanyl analogs of fluoxetine, fenfluramine, and norfenfluramine
5. Synthesis and biological evaluation of the first pentafluorosulfanyl analogs of mefloquine
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