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Cat. No. Product Name Information
PC-62511

CPI203

BET inhibitor

CPI 203 (TEN 010, JQ-2, RG-6146, RO6870810) is a primary amide analog of (+)-JQ1and a BET bromodomain inhibitor that shows cytotoxicity against MCL cell lines with GI50 of 0.1-0.3 uM.
PC-62510

BET BRD4 inhibitor Compound II-25

BRD4 BD1 inhibitor

BET BRD4 inhibitor Compound II-25 is a potent BRD4-BD1 inhibitor with IC50 of 8 nM.
PC-62475

Olinone

BET BRD1 inhibitor

Olinone is a selective inhibitor for the BET BRD1 with Kd of 3.4/3.7/8.6 uM for BRD4-BrD1/BRD3-BrD1/BRD2-BrD1, respectively, shows high selectivity over BET BRD2 (Kd>300 uM).
PC-62474

MS417

BRD4 inhibitor

MS417 (GTPL-7512) is a highly specific BET bromodomain inhibitor that binds to BRD4-BD1 and BRD4 BD2 with Kd of 36.1 uM and 25.4 uM respectively.
PC-62389

GSK1379725A

BPTF inhibitor

GSK1379725A is the first selective small molecule inhibitor of BPTF bromodomain (bromodomain PHD finger transcription factor) with Kd of 2.8 uM in a cell-based reporter assay, shows no binding activity for Brd4.
PC-62317

GW 841819X

BET inhibitor

GW 841819X is an analogue of (+)-JQ1 and a novel inhibitor of BET bromodomain that displays activity in vivo against NUT-midline carcinoma, multiple myeloma, mixed-lineage leukemia, and acute myeloid leukemia..
PC-62299

LP99

BRD7/BRD9 inhibitor

LP99 is the first potent and selective BRD7/9 bromodomain inhibitor with Kd of 99 nM for BRD9.
PC-62290

CeMMEC13

TAF1 (2) inhibitor

CeMMEC13 is a selective TAF1 second bromodomain (TAF1 (2)) inhibitor with IC50 of 2.1 uM.
PC-62289

CeMMEC1

TAF1 (2) inhibitor

CeMMEC1 is a potent, selective second bromodomain of TAF1 inhibitor with Kd of 1.8 uM.
PC-62288

CeMMEC2

BRD4 inhibitor

CeMMEC2 is a novel potent BRD4 inhibitor with IC50 of 0.9 uM, binds to both bromodomains of BRD4, comparably to (S)-JQ1.
PC-62287

BAY299

BRPF1/TAF1 inhibitor

BAY 299 is a potent and selective inhibitor of the bromodomain and PHD finger-containing (BRPF) family protein BRD1 and the second bromodomain of TAF1 with IC50 of 6 nM and 13 nM, respectively.
PC-62286

NI-57

BRPF bromodomain inhibitor

NI-57 is a potent inhibitor of the bromodomain of the BRPFs and binds to BRPF1B, BRPF2 and BRPF3 and with KD of 31 nM,108 nM and 408 nM (ITC), respectively.

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