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A biomimetic semisynthesis enables structural elucidation of selaginellin U: a tautomeric cyclic alkynylphenol from Selaginella tamariscina

机译:仿生半合成技术可以阐明卷柏(Slaginellin U)的结构:卷柏卷柏的互变异构环状炔基酚

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Two new lactone-containing selaginellins T and U ( 1 and 2 ) together with eleven known selaginellin derivatives ( 3 and 7 – 16 ) were isolated from the whole plant of Selaginella tamariscina . The structure of tautomeric selaginellin U along with its biogenetic pathway was confirmed and proposed by a cross-validation of the semisynthesis of compound 4 from selaginellin ( 3 ) and derivation from 2 to 4 . Additionally, compounds 3 , 13 and 16 exhibited good inhibitory activities against β-site amyloid precursor protein cleaving enzyme 1 (BACE1) with IC50 values of 81.17, 51.13 and 48.89?μM, respectively.
机译:从卷柏卷柏的整个植物中分离出两个新的含内酯的卷柏毒素T和U(1和2)以及11种已知的卷柏毒素衍生物(3和7-16)。互变异构的卷柏素U的结构及其生物遗传途径已通过交叉验证卷柏素(3)的化合物4的半合成和从2到4的衍生得到了交叉验证。此外,化合物3、13和16对β-位淀粉样前体蛋白裂解酶1(BACE1)表现出良好的抑制活性,IC 50 分别为81.17、51.13和48.89?μM。

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