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Description

A cell-permeable pyrroloquinoxaline compound that acts as a reversible SIRT1 activator (10 µ,M causes ~2.3-fold fluorescent enhancement in a fluorescent assay using hrSIRT1) and enhances fat mobilization in fully differentiated 3T3L1 fibroblasts. Shown to inhibit LPS-induced TNF-alpha release in THP-1 cells by ~10-fold more potent than resveratrol (Cat. No. 554325).

Structure formula

SAF-566313-10MG

Contents

Miscellaneous

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