In:
ChemMedChem, Wiley, Vol. 2, No. 9 ( 2007-09-10), p. 1339-1345
Abstract:
Research in recent years has demonstrated that the Trypanosoma cruzi cysteine protease cruzain (TCC) is a valid chemotherapeutic target. Herein we describe a small library of aryl‐4‐oxothiazolylhydrazones that have been tested in assays against T. cruzi cell cultures. The docking studies carried out suggest that these compounds are potential ligands for the TCC enzyme. The most promising compound of this series, N ‐(4‐oxo‐5‐ethyl‐2′‐thiazolin‐2‐yl)‐ N ′‐phenylthio‐( Z )‐ethylidenehydrazone ( 6 f ), was shown to be very active at non‐cytotoxic concentrations in in vitro assays with mammalian cells and has a potency comparable with reference drugs such as nifurtimox (Nfx) and benznidazole (Bdz).
Type of Medium:
Online Resource
ISSN:
1860-7179
,
1860-7187
DOI:
10.1002/cmdc.200700022
Language:
English
Publisher:
Wiley
Publication Date:
2007
detail.hit.zdb_id:
2209649-8
SSG:
15,3