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A natural product biflavonoid scaffold with anti-tryptase activity.

Authors :
Fazio NF
Russell MH
Flinders SM
Gardner CJ
Webster JB
Hansen MDH
Source :
Naunyn-Schmiedeberg's archives of pharmacology [Naunyn Schmiedebergs Arch Pharmacol] 2021 Jan; Vol. 394 (1), pp. 107-115. Date of Electronic Publication: 2020 Aug 25.
Publication Year :
2021

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.

Details

Language :
English
ISSN :
1432-1912
Volume :
394
Issue :
1
Database :
MEDLINE
Journal :
Naunyn-Schmiedeberg's archives of pharmacology
Publication Type :
Academic Journal
Accession number :
32840651
Full Text :
https://doi.org/10.1007/s00210-020-01959-2