Synthesis and in-vitro anti-leishmanial activity of (4-arylpiperazin-1-yl)(1-(thiophen-2-yl)-9 H -pyrido[3,4- b ]indol-3-yl)methanone derivatives-Reference-Cited by-同舟云学术

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Synthesis and in-vitro anti-leishmanial activity of (4-arylpiperazin-1-yl)(1-(thiophen-2-yl)-9 H -pyrido[3,4- b ]indol-3-yl)methanone derivatives

Published:2017-02 Issue: Volume:70 Page:100-106
ISSN:0045-2068
Container-title:Bioorganic Chemistry
language:en
Short-container-title:Bioorganic Chemistry

Author:

Ashok Penta,Chander Subhash,Chow Larry M.C.,Wong Iris L.K.,Singh Rajnish Prakash,Jha Prabhat Nath,Sankaranarayanan Murugesan

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Molecular Biology,Biochemistry

Reference47 articles.

1. Discovery of a new class of natural product-inspired quinazolinone hybrid as potent antileishmanial agents;Sharma;J. Med. Chem.,2013

2. Design, synthesis and biological evaluation of aryl pyrimidine derivatives as potential leishmanicidal agents;Suryawanshi;Bioorg. Med. Chem. Lett.,2013

3. Cutaneous leishmaniasis;Reithinger;Lancet Infect. Dis.,2007

4. In vitro and in vivo efficacy of novel flavonoid dimers against cutaneous leishmaniasis;Wong;Antimicrob. Agents Chemother.,2014

5. Design, synthesis and antileishmanial in vitro activity of new series of chalcones-like compounds: a molecular hybridization approach;Barbosa;Bioorg. Med. Chem.,2011

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