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Diarylcarbonates are a new class of deubiquitinating enzyme inhibitor.


ABSTRACT: Promiscuous inhibitors of tyrosine protein kinases, proteases and phosphatases are useful reagents for probing regulatory pathways and stabilizing lysates as well as starting points for the design of more selective agents. Ubiquitination regulates many critical cellular processes, and promiscuous inhibitors of deubiquitinases (DUBs) would be similarly valuable. The currently available promiscuous DUB inhibitors are highly reactive electrophilic compounds that can crosslink proteins. Herein we introduce diarylcarbonate esters as a novel class of promiscuous DUB inhibitors that do not have the liabilities associated with the previously reported compounds. Diarylcarbonates stabilize the high molecular weight ubiquitin pools in cells and lysates. They also elicit cellular phenotypes associated with DUB inhibition, demonstrating their utility in ubiquitin discovery. Diarylcarbonates may also be a useful scaffold for the development of specific DUB inhibitors.

SUBMITTER: Long MJC 

PROVIDER: S-EPMC6467287 | biostudies-literature | 2019 Jan

REPOSITORIES: biostudies-literature

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Diarylcarbonates are a new class of deubiquitinating enzyme inhibitor.

Long Marcus J C MJC   Lawson Ann P AP   Baggio Rick R   Qian Yu Y   Rozhansky Lior L   Fasci Domenico D   El Oualid Farid F   Weerapana Eranthie E   Hedstrom Lizbeth L  

Bioorganic & medicinal chemistry letters 20181128 2


Promiscuous inhibitors of tyrosine protein kinases, proteases and phosphatases are useful reagents for probing regulatory pathways and stabilizing lysates as well as starting points for the design of more selective agents. Ubiquitination regulates many critical cellular processes, and promiscuous inhibitors of deubiquitinases (DUBs) would be similarly valuable. The currently available promiscuous DUB inhibitors are highly reactive electrophilic compounds that can crosslink proteins. Herein we in  ...[more]

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