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Cat. No. Product Name Information
PC-21115

HDAC3 inhibitor 4i

HDAC3 inhibitor

HDAC3 inhibitor 4i is a potent, selective HDAC3 inhibitor with IC50 of 14 nM, shows 121-fold selectivity over HDAC1 (IC50=1983 nM) and HDAC2 (IC50=1696 nM).
PC-21042

KD5170

Class I /II HDAC inhibitor

KD5170 (KD-5170) is a potent mercaptoketone-based Class I and II-histone deacetylase (HDAC) inhibitor with IC50 of 45 nM in HeLa cell-based histone H3 hyperacetylation assay.
PC-20913

Givinostat hydrochloride monohydrate

pan HDAC inhibitor

Givinostat (ITF-2357) is a potent, orally active, pan-HDAC inhibitor with IC50 of 198 and 157 nM for HDAC1 and HDAC3, respectively.
PC-20671

TNG260

CoreDAC inhibitor

TNG260 (TNG-260) is a potent, CoREST-selective deacetylase (CoreDAC) inhibitor, inhibits HDAC1 with 10-fold selectivity over HDAC3 in cells.
PC-20479

Purinostat

Class I /IIb HDAC inhibitor

Purinostat is a potent, highly selective class I and IIb HDAC inhibitor with IC50 of 0.81, 1.4, 1.7, and 3.8 nM for class I HDAC1, 2, 3, and 8, and 11.5, 1.1 nM for class IIb HDAC 6 and 10, respectively.
PC-20478

Purinostat mesylate

Class I /IIb HDAC inhibitor

Purinostat mesylate is a potent, highly selective class I and IIb HDAC inhibitor with IC50 of 0.81, 1.4, 1.7, and 3.8 nM for class I HDAC1, 2, 3, and 8, and 11.5, 1.1 nM for class IIb HDAC 6 and 10, respectively.
PC-20402

SBI-46

HDAC inhibitor

SBI-46 (SBI 46) is an antiandrogen-equipped histone deacetylase (HDAC) inhibitor, strongly binds to androgen receptor (AR, IC50=8.4 nM) and potently inhibited HDACs and the proliferation of AR+ CRPC.
PC-20239

HO53

HDAC3 inhibitor

HO53 is a small moecule inducer of cathelicidin antimicrobial peptide gene (CAMP) expression in bronchial epithelium cells, HO53 is a histone deacetylase (HDAC) inhibitor, interacts directly with HDAC3.
PC-20238

RGFP963

class I HDAC inhibitor

RGFP963 (RGFP 963) is a potent, selective class I HDAC inhibitor with IC50 of 1.51 uM, 0.75 and 0.096 uM for HDAC1, HDAC2, and HDAC3, respectively.
PC-20237

RGFP966

HDAC3 inhibitor

RGFP966 (RGFP 966) is a potent, specific HDAC3 inhibitor with IC50 of 0.08 uM, without effective inhibition of any other HDACs at 15 uM.
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.

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