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Synthesis, and structure-activity relationship for C(4) and/or C(5) thienyl substituted pyrimidines, as a new family of antimycobacterial compounds
Research output
:
Contribution to journal
›
Article
›
peer-review
Department of Technology of Organic Synthesis
Fundamental Research Laboratory of Physiologically Active Substance
Department of Organic and Biomolecular Chemistry
Institute of Chemical Engineering
Overview
Cite this
DOI
https://doi.org/10.1016/j.ejmech.2015.05.007
Final published version
Egor V. Verbitskiy
Ekaterina M. Cheprakova
Pavel A. Slepukhin
Marionella A. Kravchenko
Sergey N. Skornyakov
Gennady L. Rusinov
Oleg N. Chupakhin
Valery N. Charushin
Original language
English
Pages (from-to)
225-234
Number of pages
10
Journal
European Journal of Medicinal Chemistry
Volume
97
DOIs
https://doi.org/10.1016/j.ejmech.2015.05.007
Publication status
Published -
5 Jun 2015
Research areas
Pyrimidine, Antimicobacterial, Tuberculosis, Cross-coupling, Nucleophilic aromatic substitution of hydrogen, MYCOBACTERIUM-TUBERCULOSIS, ANTITUBERCULOSIS ACTIVITY, COUPLING REACTIONS, ARYL BROMIDES, DERIVATIVES, INHIBITORS, ANALOGS, S-N(H), AGENTS, CHEMOTHERAPY
ASJC Scopus subject areas
Organic Chemistry
Drug Discovery
Pharmacology (medical)
Medicine(all)
ID: 342853