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Request The Product List ofBcl-2 Bcl-2

Cat. No. Product Name Information
PC-49799

BM-1197

Bcl-2/Bcl-xL inhibitor

BM-1197 (BM1197) is a potent and efficacious dual inhibitor of Bcl-2 and Bcl-xL with Ki of < 1 nM, >1,000-fold selectivity over Mcl-1.
PC-49798

Pelcitoclax

Bcl-2/Bcl-xL inhibitor

Pelcitoclax (APG-1252, BM-1252) is a potent dual specific Bcl-2/Bcl-xL inhibitor with Ki of < 1 nM, shows potent antitumor effects with minimal platelet toxicity.
PC-49791

OICR12694

Bcl-6 BTB inhibitor

OICR12694 (OICR 12694, JNJ-65234637) is a potent, selective, and orally bioavailable BCL6-BTB inhibitor with SPR KD value of 5 nM.
PC-49764

Venetoclax

Bcl-2 inhibitor

Venetoclax (ABT-199; GDC-0199) is a highly potent, selective and orally bioavailable Bcl-2 inhibitor with Ki value of <0.01 nM.
PC-49291

pBADS99 inhibitor NPB

pBAD Ser99 inhibitor

NPB (pBADS99 inhibitor NPB) is a small molecule that inhibits BCL-2-associated death promoter (BAD) phosphorylation specifically at Ser99 with IC50 of 0.41 M.
PC-38808

CCT369260

BCL6 degrader

CCT369260 is a highly potent, orally active BCL6 degrader with DC50 of 54 nM in cellular BCL6 degradation assays.
PC-38807

CCT373566

BCL6 degarder

CCT373566 is a highly potent, in vivo active BCL6 degarder with IC50 of 2.2 nM and DC50 of 0.7 nM in TR-FRET and cellular BCL6 degradation assays, respectively.
PC-38806

CCT372064

BCL6 inhibitor

CCT372064 is a potent, ligand-efficient inhibitor of BCL6 with IC50 of 3.9 nM and 12 nM in TR-FRET and cellular NanoBRET assays, respectively.
PC-38660

GSK137

BCL6 inhibitor

GSK137 is a potent, small-molecule BCL6 inhibitor binding to BCL6 BTB-POZ domain, displaces peptides derived from the human SMRT co-repressor from the BCL6 BTB-POZ domain in a TR-FRET assay with a pIC50 of 8.0.
PC-38659

WK500B

BCL6 inhibitor

WK500B is an orally available small molecule BCL6 inhibitor with IC50 of 1.39 uM (HTFR), exhibits potent efficacy against DLBCL in vitro and in vivo.
PC-73236

ZH07

Dual Mcl-1/Bfl-1 inhibitor

ZH07 (Dual Mcl-1/Bfl-1 inhibitor 24) is a potent, selective dual Mcl-1 and Bfl-1 inhibitor, binds both Mcl-1 and Bfl-1 with Ki of 97 nM and 100 nM, respectively.
PC-73235

ZH97

BFL-1 inhibitor

ZH97 is a selective and covalent small-molecule inhibitor of BFL-1 protein with binding Ki of 0.41 uM, >200-fold selectivity over MCL-1.

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