Antitrypanosomal and cytotoxic activities of 22-hydroxyclerosterol, a new sterol from Allexis cauliflora (Violaceae)

10Citations
Citations of this article
20Readers
Mendeley users who have this article in their library.

Abstract

In the search for new antiparasitic natural compounds from the medicinal plants from Cameroon, the new 22-hydroxyclerosterol, established as such on the basis of detailed chemical and spectroscopic analysis, was isolated from the hexane extract of the stem bark of Allexis cauliflora together with the known clerosterol. 22-Hydroxyclerosterol inhibited the growth of Trypanosoma brucei brucei cells with an ED50 value of 1.56 μM. The compound was also established as an uncompetitive inhibitor of the glycolytic enzyme PGI of T. brucei (Ki'= 3 ± 1 μM), an uncompetitive inhibitor of mammalian rabbit muscles' enzyme PyK (Ki'= 26 ± 3 μM) and a mixed inhibitor of PyK of Leishmania mexicana (Ki'= 65 ± 10 μM; Ki= 24 ± 5 μM). © Nganso et al.

Cite

CITATION STYLE

APA

Nganso, Y. O. D., Ngantchou, I. E. W., Nkwenoua, E., Nyasse, B., Denier, C., Hannert, V., & Schneider, B. (2011). Antitrypanosomal and cytotoxic activities of 22-hydroxyclerosterol, a new sterol from Allexis cauliflora (Violaceae). Scientia Pharmaceutica, 79(1), 137–144. https://doi.org/10.3797/scipharm.1012-10

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free