Please use this identifier to cite or link to this item: http://repositorio.unifesp.br/handle/11600/38137
Title: Triterpenoids as Novel Natural Inhibitors of Human Cathepsin L
Authors: Ramalho, Suelem D.
De Sousa, Lorena R. F.
Nebo, Liliane
Maganhi, Stella H.
Caracelli, Ignez
Zukerman-Schpector, Julio
Lima, Maria Ines S.
Alves, Marcio F. M. [UNIFESP]
Da Silva, M. Fatima das G. F.
Fernandes, Joao B.
Vieira, Paulo C.
Universidade Federal de São Carlos (UFSCar)
Universidade Federal de São Paulo (UNIFESP)
Issue Date: 1-Sep-2014
Publisher: Wiley-Blackwell
Citation: Chemistry & Biodiversity. Weinheim: Wiley-v C H Verlag Gmbh, v. 11, n. 9, p. 1354-1363, 2014.
Abstract: Cathepsins L (catL) and B play an important role in tumor progression and have been considered promising therapeutic targets in the development of novel anticancer agents. Using a bioactivity-guided fractionation, a series of triterpenoids was identified as a new class of competitive inhibitors towards cathepsin L with affinity values in micromolar range. Among the 14 compounds evaluated, the most promising were 3-epiursolic acid (3), 3-(hydroxyimino) oleanolic acid (9), and 3-(hydroxyimino) masticadienoic acid (13) with IC50 values of 6.5, 2.4, and 2.6 mu m on catL, respectively. Most of the evaluated triterpenoids do not inhibit cathepsin B. Thus, the evaluated compounds exhibit a great potential to help in the design of new inhibitors with enhanced potency and affinity towards catL. Docking studies were performed in order to gain insight on the binding mode and SAR of these compounds.
URI: http://repositorio.unifesp.br/handle/11600/38137
ISSN: 1612-1872
Other Identifiers: http://dx.doi.org/10.1002/cbdv.201400065
Appears in Collections:Em verificação - Geral

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