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Benzodiazepines and benzotriazepines as protein interaction inhibitors targeting bromodomains of the BET family.

Abstract:

Benzodiazepines are psychoactive drugs with anxiolytic, sedative, skeletal muscle relaxant and amnestic properties. Recently triazolo-benzodiazepines have been also described as potent and highly selective protein interaction inhibitors of bromodomain and extra-terminal (BET) proteins, a family of transcriptional co-regulators that play a key role in cancer cell survival and proliferation, but the requirements for high affinity interaction of this compound class with bromodomains has not been...

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Publication status:
Published

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Publisher copy:
10.1016/j.bmc.2011.10.080

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Institution:
University of Oxford
Division:
MSD
Department:
NDM
Sub department:
Structural Genomics Consortium
Role:
Author
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Journal:
Bioorganic and medicinal chemistry
Volume:
20
Issue:
6
Pages:
1878-1886
Publication date:
2012-03-01
DOI:
EISSN:
1464-3391
ISSN:
0968-0896
Source identifiers:
216127
Language:
English
Keywords:
Pubs id:
pubs:216127
UUID:
uuid:6be3a1f8-817c-41da-a01d-989803fd7146
Local pid:
pubs:216127
Deposit date:
2012-12-19

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