Synthesis and antimycobacterial properties of N-substituted 6-amino-5-cyanopyrazine-2-carboxamides-Reference-Cited by-同舟云学术

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Synthesis and antimycobacterial properties of N-substituted 6-amino-5-cyanopyrazine-2-carboxamides

Published:2011-02 Issue:4 Volume:19 Page:1471-1476
ISSN:0968-0896
Container-title:Bioorganic & Medicinal Chemistry
language:en
Short-container-title:Bioorganic & Medicinal Chemistry

Author:

Zitko Jan,Dolezal Martin,Svobodova Michaela,Vejsova Marcela,Kunes Jiri,Kucera Radim,Jilek Petr

Funder

Agency of Charles University in Prague

Ministry of Education of the Czech Republic

Publisher

Elsevier BV

Subject

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

Reference16 articles.

1. Persistent and dormant tubercle bacilli and latent tuberculosis

2. Mode of action of pyrazinamide: disruption of Mycobacterium tuberculosis membrane transport and energetics by pyrazinoic acid

3. Pyrazinamide inhibits the eukaryotic-like fatty acid synthetase I (FASI) of Mycobacterium tuberculosis

4. Inhibition of Isolated Mycobacterium tuberculosis Fatty Acid Synthase I by Pyrazinamide Analogs

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4. Pyrazinamide Analogs Designed for Rational Drug Designing Strategies against Resistant Tuberculosis;Russian Journal of Bioorganic Chemistry;2022-06

5. Regioselective Synthesis of Trisubstituted Quinoxalines Mediated by Hypervalent Iodine Reagents;The Journal of Organic Chemistry;2021-11-19

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