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新型 HS 释放双功能抗组胺药物分子,具有更好的止痒作用和降低镇静作用。

Novel HS-Releasing Bifunctional Antihistamine Molecules with Improved Antipruritic and Reduced Sedative Actions.

机构信息

Biomedical Research Foundation of the Academy of Athens, 4 Soranou Efesiou Str, Athens 115 27, Greece.

Division of Pharmaceutical Chemistry, Department of Pharmacy, National and Kapodistrian University of Athens, Panepistimiopolis Zografou, Athens 15771, Greece.

出版信息

J Med Chem. 2023 Jul 27;66(14):9607-9621. doi: 10.1021/acs.jmedchem.3c00321. Epub 2023 Jul 6.

Abstract

Hydrogen sulfide (HS) is an endogenous gasotransmitter with anti-inflammatory actions that also reduces itching. To test whether a combination of an antihistamine with a HS donor has improved antipruritic efficacy, bifunctional molecules with antihistamine and HS-releasing pharmacophores were synthesized and tested and . HS release from the hybrid molecules was evaluated with the methylene blue and lead acetate methods, and H1-blocking activity was assessed by determining tissue factor expression inhibition. All new compounds released HS in a dose-dependent manner and retained histamine blocking activity. Two compounds with the highest potency were evaluated for their antipruritic as well as sedative action; they proved to possess higher efficacy in inhibiting histamine-induced pruritus and decreased sedative effects compared to the parent compounds (hydroxyzine and cetirizine), suggesting that they exhibit superior antipruritic action and limited side effects that likely arise from the HS-releasing moiety.

摘要

硫化氢 (HS) 是一种内源性气体递质,具有抗炎作用,还可以减轻瘙痒。为了测试抗组胺药与 HS 供体的联合使用是否能提高止痒效果,合成并测试了具有抗组胺和 HS 释放药效团的双功能分子。用亚甲基蓝和醋酸铅法评估了混合分子的 HS 释放情况,并通过测定组织因子表达抑制来评估 H1 阻断活性。所有新化合物均以剂量依赖性方式释放 HS,并保留组胺阻断活性。两种活性最高的化合物被评估了其止痒和镇静作用;与母体化合物(羟嗪和西替利嗪)相比,它们在抑制组胺诱导的瘙痒方面表现出更高的疗效,并且镇静作用降低,这表明它们具有更好的止痒作用和有限的副作用,这可能是由于 HS 释放部分引起的。

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