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Cat. No. Product Name Information
PC-20160

CG13250

BET inhibitor

CG13250 (CG 13250, CG250) is a potent, selective and orally bioavailable BET bromodomain inhibitor with Kd of 44 nM (BRD4), IC50 of 1.1 uM (BRD4 BD1+BD2).
PC-20123

BI-4827

BI-4827 (BI 4827) is the negative control compound of BI-7190, which is a potent, selective chemical probe targeting the bromodomain of BPTF.
PC-20122

BI-7190

BPTF inhibitor

BI-7190 (BI 7190) is a potent, selective chemical probe targeting the bromodomain of BPTF with binding Kd of 3.5 nM.
PC-20119

BRM012

BRM/BRG1 inhibitor

BRM012 (SMARCA2/SMARCA4 inhibitor 12) is a potent inhibitor of Brahma Homolog (BRM)/SMARCA2 and Brahma-related gene 1 (BRG1/SMARCA4) with IC50 of <5 nM for both.
PC-49860

FT-6876

CBP/p300 inhibitor

FT-6876 (FT 6876) is a potent, selective, orally active CBP/p300 bromodomains inhibitor with IC50 of 5/2 nM, respectively, >500-fold selectivity over BRD4 (IC50=2,320 nM) and other bromodomains.
PC-49600

YEATS4 binder 4d

YEATS4 inhibitor

YEATS4 binder 4d is a potent, selective small-molecule epigenetic reader YEATS4 binder with Ki of 33 nM, >10-fold selectivity over YEATS1, 2 and 3.
PC-49599

YEATS4 binder 4e

YEATS4 inhibitor

YEATS4 binder 4e is a potent, selective small-molecule epigenetic reader YEATS4 binder with Ki of 37 nM, >15-fold selectivity over YEATS1, 2 and 3.
PC-49526

BAZ1A inhibitor Cpd2

BAZ1A inhibitor

BAZ1A inhibitor Cpd2 is a small molecule BAZ1A bromodomain inhibitor with KD value of 0.52 uM, displays good anti-viability activity against cancer cell lines expressing a high level of BAZ1A.
PC-49467

I-BET432

Pan-BET inhibitor

I-BET432 is a potent, highly ligand-efficient, orally active pan-BET bromodomain inhibitor with pIC50 of 7.5/7.2 for BRD4 BD1 and BD2 respectively.
PC-49366

iBRD4-BD1

BRD4-BD1 inhibitor

iBRD4-BD1 is a potent, selective inhibitor of the first BRD4 bromodomain with IC50 of 12 nM, shows 23- to 6200-fold intra-BET selectivity.
PC-49300

TDI-11055

ENL YEATS inhibitor

TDI-11055 (TDI 11055) is a potent, selective and orally bioavailable inhibitor of the acyl-lysine reader ENL/AF9 YEATS domain with IC50 of 0.05 and 0.07 uM, respectively.
PC-49278

GSK761

SP140 inhibitor

GSK761 (GSK-761) is the first small molecule inhibitor of bromodomain-containing protein SP140, inhibits macrophage inflammatory function.

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