Exploring the relationship between the physico-chemical parameters and anti-tubercular activity of quinoline-3-carboxylic acids: a QSAR approach-Reference-Cited by-同舟云学术

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Exploring the relationship between the physico-chemical parameters and anti-tubercular activity of quinoline-3-carboxylic acids: a QSAR approach

Published:2014-07-23 Issue:2 Volume:24 Page:744-752
ISSN:1054-2523
Container-title:Medicinal Chemistry Research
language:en
Short-container-title:Med Chem Res

Author:

Veerasamy Ravichandran,Chigurupati Sridevi,Sivadasan Shalini,Sokkalingam Arumugam Dhanaraj,Rajak Harish,Krishnan Suresh Kumar

Publisher

Springer Science and Business Media LLC

Subject

Organic Chemistry,General Pharmacology, Toxicology and Pharmaceutics

Link

http://link.springer.com/content/pdf/10.1007/s00044-014-1167-x.pdf

Reference28 articles.

1. Aktas E, Durmaz R, Yang D, Yang Z (2005) Molecular characterization of isoniazid and rifampin resistance of Mycobacterium tuberculosis clinical isolates from Malatya, Turkey. Microb Drug Resist 11:94–99

2. Bang D, Andersen AB, Thomsen VO (2006) Rapid genotypic detection of rifampin- and isoniazid-resistant Mycobacterium tuberculosis directly in clinical specimens. J Clin Microbiol 44:2605–2608

3. Baumann QK (2002) Distance profile: a transnationally and rotationally invariant 3D structure descriptor capturing steric properties of molecules. Struct Act Relat 21:507–519

4. Breen RAM, Miller RF, Gorsuch T et al (2006) Virological response to highly active antiretroviral therapy is unaffected by antituberculosis therapy. J Infect Dis 193:1437–1440

5. Cole ST, Brosch R, Parkhill J (1998) Deciphering the biology of Mycobacterium tuberculosis from the complete genome sequence. Nature 393:537–544

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1. Research of Anti-TB Active Compounds;PROG CHEM;2018

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