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从远东海星Lethasterias fusca中分离出的两种新海星皂苷。

Two new asterosaponins from the Far Eastern starfish Lethasterias fusca.

作者信息

Ivanchina Natalia V, Kalinovsky Anatoly I, Kicha Alla A, Malyarenko Timofey V, Dmitrenok Pavel S, Ermakova Svetlana P, Stonik Valentin A

机构信息

G.B. Elyakov Pacific Institute of Bioorganic Chemistry, Far Eastern Branch of the Russian Academy of Sciences, Vladivostok, 690022, Russian Federation.

出版信息

Nat Prod Commun. 2012 Jul;7(7):853-8.

Abstract

Two new asterosaponins, lethasteriosides A (1) and B (2), were isolated along with previously known thornasteroside A (3), anasteroside A (4), and luidiaquinoside (5) from the ethanolic extract of the Far Eastern starfish Lethasterias fusca. The structures of the new compounds were elucidated by extensive NMR and ESIMS techniques, and chemical transformations. Compounds 1 and 3-5 did not show any apparent cytotoxicity against cancer cell lines T-47D, RPMI-7951, and HCT-116, but glycoside 1, at concentration of 20 microM, demonstrated considerable inhibition of the T-47D (97%), RPMI-795I (90%) and HCT-116 (90%) cell colony formations in a soft agar clonogenic assay.

摘要

从远东海星Lethasterias fusca的乙醇提取物中分离出两种新的海星皂苷,即致死海星皂苷A(1)和B(2),以及先前已知的刺海星皂苷A(3)、无星皂苷A(4)和吕宋岛皂苷(5)。通过广泛的核磁共振(NMR)和电喷雾离子质谱(ESIMS)技术以及化学转化确定了新化合物的结构。化合物1和3 - 5对癌细胞系T - 47D、RPMI - 7951和HCT - 116未显示出任何明显的细胞毒性,但在20微摩尔浓度下,糖苷1在软琼脂克隆形成试验中对T - 47D(97%)、RPMI - 795I(90%)和HCT - 116(90%)细胞集落形成表现出显著抑制作用。

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