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芍药属植物中次要苯乙酮的聚集抑制活性。

Aggregation inhibitory activity of minor acetophenones from Paeonia species.

作者信息

Lin H C, Ding H Y, Ko F N, Teng C M, Wu Y C

机构信息

School of Pharmacy, National Defense Medical Center, Taipei, Taiwan.

出版信息

Planta Med. 1999 Oct;65(7):595-9. doi: 10.1055/s-1999-14030.

DOI:10.1055/s-1999-14030
PMID:10575372
Abstract

Two minor acetophenones, 2,5-dihydroxy-4-methoxy-acetophenone (2) and 2,5-dihydroxy-4-methylacetophenone (7) from Paeonia species were found to selectively inhibit the aggregation of rabbit platelets induced by arachidonic acid. They were more potent than the major compound, paeonol (1), and 7 also inhibited the formation of TXA2 and PGD2 from arachidonic acid.

摘要

从芍药属植物中分离得到两种次要的苯乙酮,2,5 - 二羟基 - 4 - 甲氧基苯乙酮(2)和2,5 - 二羟基 - 4 - 甲基苯乙酮(7),它们能选择性抑制花生四烯酸诱导的兔血小板聚集。它们比主要化合物丹皮酚(1)更有效,并且7还能抑制花生四烯酸生成血栓素A2(TXA2)和前列腺素D2(PGD2)。

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