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Cat. No. Product Name Information
PC-23763

IEM930

GAS41/YEATS4 inhibitor

IEM930 is a small molecule inhibitor targeting the GAS41 YEATS domain (YEATS4)) with ITC binding Kd of 32.6 uM, inhibits GAS41/ITGA4-mediated PI3K/Akt/mTOR signaling pathway in glioma cells.
PC-23754

CZL-046

p300 bromodomain inhibitor

CZL-046 is a potent, selective, and orally active p300 bromodomain inhibitor with IC50 of 3.3 nM, exhibits antiproliferative activity in the multiple myeloma (MM) cell line (OPM-2, IC50=51.5 nM).
PC-23522

XY221

BRD4 BD2 inhibitor

XY221 is a potent, BRD4 BD2-selective inhibitor with IC50 of 5.8 nM, >600-fold selective over BRD4 BD1 and 9–32-fold over BRD2/3/T BD2.
PC-23412

SR-C-107 (R)

ENL YEATS inhibitor

SR-C-107 (R) is a highly potent YEATS domain-containing protein ENL (Eleven-Nineteen-Leukemia) with IC50 of 40 nM, binding KD of 144 nM.
PC-22992

Y06014

BET inhibitor

Y06014 is a selective BRD4(1) inhibitor with IC50 of 4.87 uM.
PC-22925

GSK2801

BAZ2A/B inhibitor

GSK2801 is a potent, selective and cell active acetyl-lysine competitive inhibitor of BAZ2A and BAZ2B bromodomains with KD values of 136 and 257 nM for BAZ2B and BAZ2A, respectively.
PC-22528

I-BET469

BET inhibitor

I-BET469 is a potent, selective pan-BET bromodomain inhibitor with pIC50 of 7.9 for BRD4 BD1, >5000-fold selective over BAZ2A.
PC-22527

I-BET787

BET inhibitor

I-BET787 (GSK3535787) is potent, efficient pan-BET bromodomain inhibitor with pIC50 of 7.1/5.9 for BRD4 BD1/BD2, respectively.
PC-22485

Y08284

CBP/p300 inhibitor

Y08284 is a potent, selective CBP/p300 bromodomain inhibitor with IC50 of 4.21 nM (CBP bromodomain) in HTRF assays.
PC-22484

Y08207

CBP/p300 inhibitor

Y08207 is a potent, selective CBP/p300 bromodomain inhibitor with IC50 of 26.37 nM (CBP bromodomain) in HTRF assays.
PC-22483

Y08262

CBP/p300 inhibitor

Y08207 is a potent, selective CBP/p300 bromodomain inhibitor with IC50 of 73.1 nM (CBP bromodomain) in HTRF assays.
PC-22287

CDD-1302

BRDT BD2 inhibitor

CDD-1302 (CDD1302) is a potent, selective second bromodomain (BD2) of BRDT and BRD4 inhibitor with IC50 of 8 and 12 nM, >1,000-fold and 300-fold selectivity over BRDT-BD1 and BRD4-BD1.

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