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Cat. No. Product Name Information
PC-42421

EDO-S101

HDAC inhibitor

EDO-S101 (Tinostamustine) is a fusion molecule comprising of the alkylator bendamustine and the HDAC-inhibitor vorinostat.
PC-42767

PCI-24781

HDAC inhibitor

PCI-24781 (Abexinostat, CRA 024781) is a broad spectrum HDAC inhibitor, inhibits pure recombinant HDAC1 with Ki of 7 nM.
PC-42126

HDACi-4b

HDAC inhibitor

A benzamide-type HDAC inhibitor with IC50 of 78 uM for changes of FXN mRNA in affected GM15850 cells.
PC-23348

PB131

HDAC6 inhibitor

PB131 is a potent, selective and brain-permeable HDAC6 inhibitor with IC50 of 1.8 nM, <100-fold selective over other HDAC isoforms.
PC-22845

HQ-30

HDAC3 inhibitor, PD-L1 degrader

HQ-30 is a potent, dual-acting HDAC3 inhibitor (IC50=89 nM) and PD-L1 degrader (DC50=5.7 uM, Dmax=80% at 10 uM).
PC-22801

HDAC6 inhibitor 5a

HDAC6 inhibitor

HDAC6 inhibitor 5a (MPI-5a) is potent and selective HDAC6 inhibitor with IC50 of 36 nM, >50-fold selectivity over other HDACs
PC-22791

Givinostat

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-22782

Leuxinostat

HDAC6 inhibitor

Leuxinostat is a potent, specific HDAC6 inhibitor with IC50 of 30 nM, induces apoptosis in FLT3-ITD AML cells.
PC-22672

SP-1-303

HDAC inhibitor, ATM activator

SP-1-303 is a dual-targeting class I HDAC inhibitor and ATM activator with IC50 of 12/14 nM for HDAC1/3, preferentially inhibits ER+ breast cancer growth.
PC-22549

NT376

class IIa HDAC inhibitor

NT376 is a highly potent, selective class-IIa HDACs inhibitor with cellular IC50 of 32 nM in HT-29 cell line, >100-fold selectivity over other HDAC classes.
PC-22482

Bufexamac

HDAC6/10 inhibitor

Bufexamac (Bufexamic acid) is a selective class IIb (HDAC6, HDAC10) HDAC inhibitor with Kd of 0.53 µM and 0.22 µM respectively, also is a nonsteroida anti-inflammatory agent targeting LTA4H.
PC-22427

PCI-34051

HDAC8 inhibitor

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

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