Description
An HDAC inhibitor (IC50s = 29 nM, 62 nM, and 1.09 µM for HDAC1, 2, and 3, respectively); possesses preferential binding kinetics with seven-fold longer half-life on HDAC2 compared to HDAC1 (143 min vs. 20 min)
Formal name: N-(4-amino-4′-fluoro[1,1′-biphenyl]-3-yl)tetrahydro-2H-pyran-4-carboxamide
Synonyms:
Molecular weight: 314.4
CAS: 1404559-91-6
Purity: ≥98%
Formulation: A crystalline solid
Product Type|Biochemicals|Small Molecule Inhibitors|Deacetylases||Research Area|Epigenetics, Transcription, & Translation|Erasers|Histone Deacetylation||Research Area|Neuroscience|Neurodegenerative Disorders