z-logo
open-access-imgOpen Access
Synthesis of simple molecules prepared as arginase inhibitors and evaluated against Leishmania amazonensis
Author(s) -
Nuacute bia Boechat
Publication year - 2013
Publication title -
journal of microbiology and antimicrobials
Language(s) - English
Resource type - Journals
ISSN - 2141-2308
DOI - 10.5897/jma2013.0261
Subject(s) - arginase , docking (animal) , chemistry , leishmania , combinatorial chemistry , molecular model , amidine , thiourea , enzyme , computational biology , biochemistry , stereochemistry , organic chemistry , biology , amino acid , arginine , computer science , medicine , parasite hosting , nursing , world wide web
In this work, we synthesized substances and evaluated the potential leishmanicidal activity. Thirty-four (34) compounds from different chemical classes were selected for a simple synthesis in overall good yields, eight of which are not described in the literature. From the 34 compounds evaluated for preliminary leishmanicidal activity, three can be considered as prototypes for the development of leishmanicidal agents. Computational chemistry calculations, including comparative modeling of the enzyme arginase from Leishmania amazonensis and a molecular docking simulation of the synthesized molecules into the active site of the model were carried out.   Key words: Leishmaniasis, arginase, molecular docking, thiourea, bisguanidine, amidine, biological evaluation, comparative modeling

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom