88775-43-3Relevant articles and documents
Synthesis, characterization and antimicrobial activities of chalcones and their post transformation to pyrazole derivatives
Ramyashree,Raghavendra,Dileep Kumar,Vagish,Ajay Kumar
, p. 1538 - 1542 (2017/05/29)
An efficient procedure for the synthesis of trisubstituted pyrazoles was developed. Claisen-Schmidt condensation of 2,4,5-trimethoxybenzaldehyde and substituted acetophenone in the presence of aqueous alkaline bases produced chalcones. The cyclocondensati
Biochemical evaluation of a series of synthetic chalcone and hydrazide derivatives as novel inhibitors of cruzain from trypanosoma cruzi
Borchhardt, Deise M.,Mascarello, Alessandra,Chiaradia, Louise Domeneghini,Nunes, Ricardo J.,Oliva, Glaucius,Yunes, Rosendo A.,Andricopulo, Adriano D.
experimental part, p. 142 - 150 (2010/08/22)
Chagas' disease, a parasitic infection widely distributed throughout Latin America, is a major public health problem with devastating consequences in terms of human morbidity and mortality. The enzyme cruzain is the major cysteine protease from Trypanosoma cruzi, the etiologic agent of American trypanosomiasis or Chagas' disease, and has been selected as an attractive target for the development of novel trypanocidal drugs. In the present work, we describe the synthesis and inhibitory effects of a series of thirty-three chalcone and seven hydrazide derivatives against the enzyme cruzain from T. cruzi. Most of the compounds showed promising in vitro inhibition (IC50 values in the range of 20-60 μM), which suggest the potential of these compounds as lead candidates for further development. Twelve compounds have not been reported before, and four of them (7, 13, 16 e 18) are among the most potent inhibitors of the series.
