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CAS No. | 1235859-13-8 | Cat. No. | BCP44113 |
Name | CHR-3996 | ||
Synonyms | CHR3996;CHR 3996; | ||
SMILES | C1C(CC2C1C2NCC3=NC4=C(C=C3)C=C(C=C4)F)C5=NC=C(C=N5)C(=O)NO | ||
Chemical Name | |||
Formula | C21H20FN5O2 | M. Wt | 393.41 |
Purity | 98% | Storage | Store at 4-8°C |
Description | CHR-3996 is an orally bioavailable, second-generation hydroxamic acid-based inhibitor of histone deacetylase (HDAC) with potential antineoplastic activity. HDAC inhibitor CHR-3996 inhibits HDAC, resulting in an accumulation of highly acetylated histones, the induction of chromatin remodeling, and the selective transcription of tumor suppressor genes; these events may result in the inhibition of tumor cell division and the induction of tumor cell apoptosis. This agent may upregulate HSP70 and downregulate anti-apoptotic Bcl-2 proteins more substantially than some first-generation HDAC inhibitors. HDACs, upregulated in many tumor cell types, are a family of metalloenzymes responsible for the deacetylation of chromatin histone proteins. |
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