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具有抗胰蛋白酶活性的天然产物二氢黄酮骨架。

A natural product biflavonoid scaffold with anti-tryptase activity.

机构信息

Department of Physiology and Developmental Biology, Brigham Young University, 4005 LSB, Provo, UT, 84602, USA.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 2021 Jan;394(1):107-115. doi: 10.1007/s00210-020-01959-2. Epub 2020 Aug 25.

Abstract

Tryptase is a serine protease that is released from mast cells during allergic responses. Tryptase inhibitors are being explored as treatments for allergic inflammation in the skin and respiratory system, most notably asthma. Here we report direct tryptase inhibition by natural product compounds. Candidate inhibitors were identified by computational screening of a large (98,000 compounds) virtual library of natural product compounds for tryptase enzymatic site binding. Biochemical assays were used to validate the predicted anti-tryptase activity in vitro, revealing a high (four out of six) success rate for predicting binding using the computational docking model. We further assess tryptase inhibition by a biflavonoid scaffold, whose structure-activity relationship is partially defined by assessing the potency of structurally similar analogs.

摘要

类胰蛋白酶是一种丝氨酸蛋白酶,在过敏反应期间从肥大细胞中释放出来。类胰蛋白酶抑制剂正在被探索作为治疗皮肤和呼吸系统过敏炎症的方法,尤其是哮喘。在这里,我们报告了天然产物化合物对类胰蛋白酶的直接抑制作用。候选抑制剂是通过对天然产物化合物的大型(98000 种化合物)虚拟文库进行计算筛选,以寻找与类胰蛋白酶酶活性部位结合的化合物而确定的。生化测定用于体外验证预测的抗类胰蛋白酶活性,表明使用计算对接模型预测结合的成功率很高(四分之六)。我们进一步评估了双黄酮支架的类胰蛋白酶抑制作用,其结构-活性关系部分通过评估结构相似的类似物的效力来确定。

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