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Cat. No. Product Name Information
PC-20197

TTA03-107

HDAC1 inhibitor

TTA03-107 is a potent, selective HDAC1 inhibitor with Ki of 3.22 and 17.6 nM for HDAC1/2, respectively.
PC-49844

NBM-T-L-BMX-OS01

HDAC8 inhibitor

NBM-T-L-BMX-OS01 (BMX, HDAC8 inhibitor) is a potent, selective and BB penetrant HDAC8 inhibitor with IC50 of 831 nM.
PC-49539

GH8HA01

HDAC8 inhibitor

GH8HA01 is a highly potent, selective HDAC8 inhibitor with Ki of 0.67 nM, highly selective against HDAC8 compared to other HDACs.
PC-49363

DKFZ-748

HDAC10 inhibitor

DKFZ-748 (DKFZ748) is a potent, specific HDAC10 inhibitor with cellular IC50 of 22 nM, >500-fold selectivity over other HDAC isozymes.
PC-38796

A452

HDAC6 inhibitor

A452 is a potent and selective HDAC6 inhibitor, effectively inhibits the cell growth and viability of various cancer cell types, irrespective of p53 status.
PC-73193

Rocilinostat

HDAC6 inhibitor

Ricolinostat (ACY-1215) is a potent and selective HDAC6 inhibitor with IC50 of 5 nM.
PC-72875

MJM-1

HDAC inhibitor

MJM-1 is a small-molecule brain-penetrant HDAC inhibitor that increases the overall level of histone 3 (H3) acetylation in prostate cancer cell line.
PC-72740

NN-390

HDAC6 inhibitor.

NN-390 (NN390) is a potent, selective HDAC6 inhibitor with IC50 of 9.8 nM, >200-550-fold selectivity over other HDAC isoforms.
PC-72144

Splitomicin

Sir2p inhibitor

Splitomicin is a selective Sir2p inhibitor, inhibits NAD+-dependent histone deacetylase activity (HDA) of the Sir2 protein wqith IC50 of 60 uM.
PC-35666

Class I and IIB HDAC inhibitor 42

Class I and IIB HDAC inhibitor 42 is a novel potent, selective class I and IIB inhibitor (HDAC1 Ki=0.27 nM) for topical treatment of cutaneous t-cell lymphoma..
PC-63481

HDAC8-IN-22d

HDAC8-IN-22d is a potent, selective HDAC8 inhibitor with IC50 of 27.2 nM, exhibits no activity against other HDACs and limited activity against HDAC1 and 3.
PC-42249

HDAC-IN-4

A histone deacetylase (HDAC) inhibitor, extracted from patent WO/2007045844 A1..

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