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.
CITATION STYLE
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
Mendeley helps you to discover research relevant for your work.