Design, synthesis and in vitro trypanocidal and leishmanicidal activities of novel semicarbazone derivatives-Reference-Cited by-同舟云学术

Design, synthesis and in vitro trypanocidal and leishmanicidal activities of novel semicarbazone derivatives

Published:2015-07 Issue: Volume:100 Page:24-33
ISSN:0223-5234
Container-title:European Journal of Medicinal Chemistry
language:en
Short-container-title:European Journal of Medicinal Chemistry

Author:

Alves Marina A.,de Queiroz Aline C.,Alexandre-Moreira Magna Suzana,Varela Javier,Cerecetto Hugo,González Mercedes,Doriguetto Antonio C.,Landre Iara M.,Barreiro Eliezer J.,Lima Lídia M.

Funder

CNPq (BR), FAPERJ (BR), FAPEAL (BR)

INCT-INOFAR

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Pharmacology,General Medicine

Reference43 articles.

1. Trypanosomatid parasites causing neglected diseases;Nussbaum;Curr. Med. Chem.,2010

2. http://www.who.int/neglected_diseases/diseases/en/, (accessed 28.10.14.).

3. The genome sequence of Trypanosoma cruzi, etiologic agent of Chagas disease;El-Sayed;Science,2005

4. Synthesis and biological evaluation of novel 2,3-disubstituted quinoxaline derivatives as antileishmanial and antitrypanosomal agents;Cogo;Eur. J. Med. Chem.,2015

5. Synthesis and in vitro activity of limonene derivatives against Leishmania and Trypanosoma;Graebin;Eur. J. Med. Chem.,2010

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