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Cat. No. Product Name Information
PC-26064

UVI5008

Epigenetic inhibitor

UVI5008 is a small molecule epigenetic modifier/modulator that inhibits histone deacetylases, sirtuins, and DNA methyltransferases, affects the death receptor (DR) pathway and reactive oxygen species (ROS) production in cancer cells.
PC-25935

Colrestat

class I HDAC inhibitor

Colrestat is a potent, selective inhibitor of class I histone deacetylases (HDACs) with IC50 of 41.2 nM, 52.5 nM and 74.3 nM for HDAC1, HDAC2 and HDAC3 respectively.
PC-25904

Mesinostat

HDAC6 inhibitor

Mesinostat is a potent and selective HDAC6 inhibitor with IC50 of 7.7 nM, >200-fold selective over HDAC1.
PC-25868

EKZ-438

HDAC6 inhibitor

EKZ-438 is a potent, selective, CNS-penetrant and orally bioavailable HDAC6 inhibitor with IC50 of 12 nM, >8,500-fold selectivity for HDAC6 versus all other HDAC6 paralogs.
PC-25412

SYSUP007

HDAC inhibitor

SYSUP007 is a derivative of the FTO inhibitor rhein, and HDAC and SGK1 inhibitor, inhibits the proliferation of human GBM cells.
PC-25166

DAC-001

HDAC1 activator

DAC-001 is a small molecule, cell-active activator of HDAC1, exhibits dose-dependent activation of HDAC1 in vitro in a microfluidics-based assay at 5-10 uM, displayes significant protection against DNA breaks.
PC-25165

DAC-003

HDAC1 activator

DAC-003 is a small molecule activator of HDAC1, exhibits dose-dependent activation of HDAC1 in vitro in a microfluidics-based assay at 5-10 uM, DAC-003 is protective against oxidative stress.
PC-25161

CBUD-1001

HDAC1 inhibitor

CBUD-1001 is specific small molecule HDAC1 inhibitor with IC50 of 28.1 nM, inhibits HDAC2 and HDAC3 with IC50 values of 158 nM and 404 nM, respectively.
PC-25122

Dual Hsp90-HDAC6 inhibitor 17

Hsp90/HDAC6 inhibitor

Dual Hsp90/HDAC6 inhibitor 17 is a potent, selective dual Hsp90/HDAC6 inhibitor with IC50 of 28/96 nM respectively.
PC-25111

Martinostat hydrochloride

HDAC inhibitor

Martinostat hydrochloride is a potent, selective inhibitor for class I and class-IIb HDACs with IC50 of 0.3/2.0/0.6 nM for HDAC1/2/3 and 4.1 nM for HDAC6 respectively, >100-fold selectivity over other HDAC isoforms.
PC-24898

TNI-97

HDAC6 inhibitor

TNI-97 is a potent, highly selective and orally bioavailable HDAC6 inhibitor with IC50 of 0.2 nM.
PC-24776

ITF3107

HDAC6 inhibitor

ITF3107 is a potent, selective HDAC6 inhibitor with IC50 of 5 nM, >70-fold more selective for HDAC6over HDAC1/2/3.

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