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Cat. No. Product Name Information
PC-60028

A-485

p300/CBP inhibitor

A-485 (A485) is a potent, selective and, cell and in vivo active p300/CBP catalytic inhibitor with IC50 of 9.8/2.6 nM.
PC-45646

I-CBP112

CBP/p300 inhibitor

I-CBP112 is a specific and potent inhibitor of CBP/p300 bromodomain with Kd of 150-170 nM.
PC-21986

EPIC-0628

HOTAIR-EZH2 inhibitor

EPIC-0628 (EPIC0628) is a selective and potent inhibitor that selectively disrupts the HOTAIR-EZH2 interaction and promotes ATF3 expression, enhances the temozolomide efficacy in glioblastoma.
PC-21843

SGF29 inhibitor DC60

SGF29 inhibitor

SGF29 inhibitor DC60 is a small molecule inhibitor of Spt-Ada-Gcn5 acetyltransferase (SAGA)-associated factor 29 (SGF29, CCDC101) with IC50 of 6.4 uM, binds to SGF29 second Tudor domain (SGF29 Tudor 2) and blocks SGF29 chromatin binding domain.
PC-20867

MG149

Tip60 (KAT5) inhibitor

MG149 is a selective histone acetyltransferase Tip60 (KAT5) inhibitor with IC50 of 74 uM, with no activity against PCAF and p300.
PC-20778

C646

p300 inhibitor

C646 is a selective, competitive histone acetyltransferase (HAT) p300 inhibitor with Ki of 400 nM, less potent for other acetyltransferases.
PC-20777

MC4171

KAT8 inhibitor

MC4171 (KAT8 inhibitor 34) is a first-in-class, selective and reversible lysine acetyltransferase KAT8 inhibitor with IC50 of 8.1 uM and SPR Kd of 2.04 uM.
PC-49530

DS-9300

EP300/CBP inhibitor

DS-9300 (DS9300) is a highly potent, selective and orally active EP300/CBP histone acetyltransferase (HAT) inhibitor with IC50 of 28 nM, inhibits cellular acetylation of histone H3K27 (H3K27Ac) with IC50 of 54 nM.
PC-72364

Cholera Toxin B subunit

p300 activator

Cholera Toxin B subunit (CTB) is a small molecule activator of p300 HAT enzyme, stimulats the expression of p300.
PC-72239

CCT077791

PCAF inhibitor

CCT077791 (CCT077791) is a small molecule inhibitor of PCAF and p300 histone acetyltransferase with IC50 of 2.2 uM and IC95 of 35 uM, respectively.
PC-72165

CPI-1612

EP300/CBP inhibitor

CPI-1612 (CPI 1612) is a highly potent, selective, orally bioavailable EP300/CBP histone acetyltransferase inhibitor with IC50 of 8.1 nM (EP300 HAT SPA).

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