化学
白桦素
三萜类
磷酸二酯酶
抑制性突触后电位
立体化学
生物化学
酶
神经科学
生物
作者
И. А. Толмачева,Daria V. Eroshenko,Irina A. Chernyshova,М. А. Назаров,Olga I. Lavrik,Victoria V. Grishko
标识
DOI:10.1016/j.ejmech.2024.116724
摘要
For the first time, a synthetic route for preparing lupane and oleanane derivatives with a hydrogenated furan ring as a cycle A of triterpene scaffold is described. Most of the synthesized compounds, furanoterpenoids and their synthetic intermediates, were non-toxic against the tested cancer and non-cancerous cell lines, and evinced significant inhibitory activity with IC
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