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萱草根中的甾体糖苷及其抗血小板聚集活性。

Steroidal glycosides from the rhizomes of Anemarrhena asphodeloides and their antiplatelet aggregation activity.

机构信息

Department of Biotechnology, Beijing Institute of Radiation Medicine, No. 27 Taiping Road, Beijing, P. R. China.

出版信息

Planta Med. 2012 Apr;78(6):611-6. doi: 10.1055/s-0031-1298223. Epub 2012 Feb 3.

Abstract

Five new steroidal glycosides, timosaponin J ( 1), timosaponin K ( 2), (25 S)-karatavioside C ( 5), timosaponin L ( 6), and (25 S)-officinalisnin-I ( 8), together with eight known steroidal saponins, timosaponin E (1) ( 3), purpureagitosid ( 4), timosaponin BII ( 7), timosaponin B III ( 9), anemarrhenasaponin I ( 10), anemarrhenasaponin III ( 11), anemarrhenasaponin A (2) ( 12), and timosaponin A III ( 13), were isolated from the rhizomes of Anemarrhena asphodeloides. Their structures were elucidated on the basis of spectroscopic and chemical evidence. The aglycones of compounds 1 and 2 are new aglycones. Compounds 1- 13 were evaluated for their platelet aggregation activities, and compound 13 exhibited the strongest inhibitory effect on adenosine diphosphate (ADP)-induced platelet aggregation.

摘要

从知母根茎中分离得到了五个新甾体糖苷,分别为知母皂苷 J(1)、知母皂苷 K(2)、(25S)-karatavioside C(5)、知母皂苷 L(6)和(25S)-officinalisnin-I(8),以及八个已知甾体皂苷,分别为知母皂苷 E(1)(3)、紫菀糖苷(4)、知母皂苷 BII(7)、知母皂苷 BIII(9)、菝葜皂苷 I(10)、菝葜皂苷 III(11)、菝葜皂苷 A(2)(12)和知母皂苷 AIII(13)。这些化合物的结构是通过光谱和化学证据确定的。化合物 1 和 2 的糖苷配基是新的糖苷配基。对化合物 1-13 进行了血小板聚集活性评价,化合物 13 对二磷酸腺苷(ADP)诱导的血小板聚集有最强的抑制作用。

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