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具有H1抗组胺和肥大细胞稳定特性的3-硝基-4-羟基香豆素的N-苄基哌嗪衍生物。

N-benzylpiperazino derivatives of 3-nitro-4-hydroxycoumarin with H1 antihistamine and mast cell stabilizing properties.

作者信息

Buckle D R, Outred D J, Smith H, Spicer B A

出版信息

J Med Chem. 1984 Nov;27(11):1452-7. doi: 10.1021/jm00377a013.

Abstract

In a small range finding study a number of N-benzylpiperazino derivates of 3-nitro-4-hydroxycoumarin have been shown to combine potent H1-antihistamine activity with that of mast cell stabilization as demonstrated by their activity as antagonists of histamine on guinea pig ileum and by their inhibition of the release of histamine in rat passive peritoneal anaphylaxis (PPA). The most potent compound, 1-[2-hydroxy-3-[(4-hydroxy-3-nitrocoumarin-7-yl)oxy]propyl]-4- (4-chlorobenzyl)piperazine, 30, had a pA2 of 9.0 against histamine on guinea pig ileum and inhibited histamine release in the rat PPA test with a potency similar to that of disodium cromoglycate.

摘要

在一项小型的效能研究中,已表明多种3-硝基-4-羟基香豆素的N-苄基哌嗪衍生物兼具强效H1-抗组胺活性和肥大细胞稳定活性,这通过它们对豚鼠回肠组胺的拮抗活性以及对大鼠被动腹膜过敏反应(PPA)中组胺释放的抑制作用得以证明。最有效的化合物1-[2-羟基-3-[(4-羟基-3-硝基香豆素-7-基)氧基]丙基]-4-(4-氯苄基)哌嗪(30)对豚鼠回肠组胺的pA2为9.0,并且在大鼠PPA试验中抑制组胺释放的效能与色甘酸二钠相似。

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