کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1397267 | 1501114 | 2015 | 6 صفحه PDF | دانلود رایگان |
• Triterpene natural products are proposed as a new class of compounds for blocking HCV entry.
• The structure diversity of echinocystic acid was expanded via ring A and/or C expansion/opening reaction.
• Ring A and C are highly conserved, any modification might significantly decrease or even eliminate its activity.
Echinocystic acid (EA), a naturally occurring oleanane-type triterpene isolated from Dipsacus asperoides, was found to have anti-HCV entry activity in our previous study. Expansion of triterpene structural diversity, including the ring A and/or C expansion and opening, was performed. To elucidate the pharmacophore of EA, seven lactones (8, 16, 17, 24, 26, 35 and 41), three 3,28-dioic acids (9, 36 and 42) and two pentols (10 and 27) were synthesized. The anti-HCV entry activities of those derivatives, along with their parental compound EA and analogs α,β-unsaturated ketone (18), were evaluated. All the products showed no improvement but detrimental effect on potency of EA. The results demonstrated that ring A and C of EA are highly conserved, indicating the steric effects of the rigid skeleton have a profound effect on the potency.
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Journal: European Journal of Medicinal Chemistry - Volume 102, 18 September 2015, Pages 594–599