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Selectivity of inhibitors of endocannabinoid biosynthesis evaluated by activity-based protein profiling.


ABSTRACT: The endocannabinoid 2-arachidonoylglycerol (2-AG) has been implicated as a key retrograde mediator in the nervous system based on pharmacological studies using inhibitors of the 2-AG biosynthetic enzymes diacyglycerol lipase alpha and beta (DAGL-alpha/beta). Here, we show by competitive activity-based protein profiling that the DAGL-alpha/beta inhibitors, tetrahydrolipstatin (THL) and RHC80267, block several brain serine hydrolases with potencies equal to or greater than their inhibitory activity against DAGL enzymes. Interestingly, a minimal overlap in target profiles was observed for THL and RHC80267, suggesting that pharmacological effects observed with both agents may be viewed as good initial evidence for DAGL-dependent events.

SUBMITTER: Hoover HS 

PROVIDER: S-EPMC2634297 | biostudies-literature | 2008 Nov

REPOSITORIES: biostudies-literature

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Selectivity of inhibitors of endocannabinoid biosynthesis evaluated by activity-based protein profiling.

Hoover Heather S HS   Blankman Jacqueline L JL   Niessen Sherry S   Cravatt Benjamin F BF  

Bioorganic & medicinal chemistry letters 20080702 22


The endocannabinoid 2-arachidonoylglycerol (2-AG) has been implicated as a key retrograde mediator in the nervous system based on pharmacological studies using inhibitors of the 2-AG biosynthetic enzymes diacyglycerol lipase alpha and beta (DAGL-alpha/beta). Here, we show by competitive activity-based protein profiling that the DAGL-alpha/beta inhibitors, tetrahydrolipstatin (THL) and RHC80267, block several brain serine hydrolases with potencies equal to or greater than their inhibitory activit  ...[more]

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