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苯恶洛芬[2-(4-氯苯基)-α-甲基-5-苯并恶唑乙酸]——一种脂氧合酶抑制剂的抗过敏活性。

The anti-allergic activity of Benoxaprofen [2-(4-chlorophenyl)-alpha-methyl-5-benzoxazole acetic acid]--a lipoxygenase inhibitor.

作者信息

Boot J R, Sweatman W J, Cox B A, Stone K, Dawson W

出版信息

Int Arch Allergy Appl Immunol. 1982;67(4):340-3. doi: 10.1159/000233044.

Abstract

Benoxaprofen [2-(4-chlorophenyl)-alpha-methyl-5-benzoxazole acetic acid], a novel anti-inflammatory compound, is also an orally-active anti-allergic compound in animals. It reduced the anaphylactic release of mediators, particularly slow-reacting substance of anaphylaxis (SRS-A), from both in vitro and in vivo animal models. Benoxaprofen marginally antagonized the activity of histamine on the guinea pig ileum, but not of SRS-A, at concentrations which inhibited the release of SRS-A.

摘要

苯恶洛芬[2-(4-氯苯基)-α-甲基-5-苯并恶唑乙酸]是一种新型抗炎化合物,在动物体内也是一种口服活性抗过敏化合物。它能减少体外和体内动物模型中介导物的过敏反应释放,尤其是过敏反应慢反应物质(SRS-A)。在抑制SRS-A释放的浓度下,苯恶洛芬对组胺在豚鼠回肠上的活性有轻微拮抗作用,但对SRS-A没有。

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