tcsc1277 PCI-34051

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Product Description

PCI-34051 is a potent and selective HDAC8 inhibitor with IC50 of 10 nM, with >200-fold selectivity over the other HDAC isoforms.









IC50 & Target: IC50: 10 nM (HDAC8), 2.9 μM (HDAC6), 4 μM (HDAC1), 13 μM (HDAC10)[1]

In Vitro: PCI-34051 inhibits pure recombinant HDAC8 with Ki of 10 nM with >200-fold selectivity over the other HDACs tested, including HDACs 1, 2, 3, 6 and 10. PCI-34051 is derived from a low molecular weight hydroxamic acid scaffold that possessed promising potency (HDAC8; Ki=2 μM) and selectivity (approximately fivefold) for HDAC8 relative to the other class I HDACs. PCI-34051 is found to induce apoptosis at low micromolar concentrations in cell lines derived from T-cell lymphomas, including Jurkat and HuT78, whereas doses as high as 20 μM has no effect on B-cell- or myeloid-derived lymphomas or solid tumor lines[1].





In Vivo: Administration of PCI-34051 and Dexamethasone reduces the eosinophilic inflammation and airway hyperresponsiveness in asthma to reduce the airway remodeling[2].

Information

CAS No950762-95-5
FormulaC17H16N2O3
Clinical Informationclinicalinformation
PathwayEpigenetics
Cell Cycle/DNA Damage
TargetHDAC
HDAC

Specifications

Purity / Grade>98%
SolubilityDMSO : ≥ 30 mg/mL (101.24 mM)
Smilessmiles

Misc Information

Observed Molecular Weight296.32
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