倍半萜
倍半萜内酯
无鞭毛体
锑葡胺
植物化学
IC50型
立体化学
传统医学
菊科
化学
利什曼原虫
蒿属
生物
植物
体外
利什曼病
生物化学
皮肤利什曼病
医学
寄生虫寄主
免疫学
计算机科学
万维网
作者
Maryam Fattahian,Mustafa Ghanadian,Behzad Zolfaghari,Sara Abdeyazdan,Sedigheh Saberi,Fazila Zulfiqar,Ikhlas A. Khan,Zulfıqar Ali
标识
DOI:10.1080/14786419.2022.2102630
摘要
Two new eudesmane-type sesquiterpene lactones, 1β,3α,8α-trihydroxy-11β,13-dihydroeudesma-4(15)-en-12,6α-olide (1) and 1β,4α,8α-trihydroxy-11β,13-dihydroeudesma-12,6α-olide (2), and an unprecedented elemane-type sesquiterpene lactone, 1β,2β,8α-trihydroxy-11β,13-dihydroelema-12,6α-olide (3) along with a known eudesmanolide artapshin (4) were isolated from Seriphidium khorassanicum. Structures were elucidated by NMR, HR-ESI-MS, and ECD spectral data analysis. The anti-protozoal activity was evaluated against Leishmania major promastigotes and amastigote-infected macrophages. They showed dose- and time-dependent activity against L. major amastigotes with IC50 values in the range of 4.9 to 25.3 μM being favourably far below their toxicity against normal murine macrophages with CC50 values ranging from 432.5 to 620.7 μM after 48 h of treatment. Compound 3 exhibited the strongest activity and the highest selectivity index (SI) with IC50 of 4.9 ± 0.6 μM and SI of 88.2 comparable with the standard drug, meglumine antimoniate (Glucantime), with IC50 and SI values of 15.5 ± 2.1 μM and 40.0, respectively.
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