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3,5-Dimethylisoxazoles inhibit...
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3,5-Dimethylisoxazoles inhibit the bromodomain-histone protein-protein interaction
Manylion Llyfryddiaeth
Prif Awduron:
Hewings, D
,
Wang, M
,
Philpott, M
,
Fedorov, O
,
Uttarkar, S
,
Filippakopoulos, P
,
Picaud, S
,
Vuppusetty, C
,
Marsden, B
,
Heightman, T
,
Knapp, S
,
Brennan, P
,
Conway, S
Fformat:
Conference item
Cyhoeddwyd:
2012
Daliadau
Disgrifiad
Eitemau Tebyg
Dangos Staff
Eitemau Tebyg
3,5-dimethylisoxazoles act as acetyl-lysine-mimetic bromodomain ligands.
gan: Hewings, D, et al.
Cyhoeddwyd: (2011)
3,5-dimethylisoxazoles act as acetyl-lysine-mimetic bromodomain ligands
gan: Hewings, D, et al.
Cyhoeddwyd: (2011)
Developing chemical probes for the BET bromodomains
gan: Hewings, D, et al.
Cyhoeddwyd: (2012)
Optimization of 3,5-dimethylisoxazole derivatives as potent bromodomain ligands.
gan: Hewings, D, et al.
Cyhoeddwyd: (2013)
The design and synthesis of 5-and 6-isoxazolylbenzimidazoles as selective inhibitors of the BET bromodomains
gan: Hay, D, et al.
Cyhoeddwyd: (2013)