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Cat. No. Product Name Information
PC-61318

(-) BI97D6

BCL-2 inhibitor

(-) BI97D6 (BI112D1) is a potent, pan-active inhibitor of Bcl-2 family proteins with IC50 of 76, 31, 25, and 122 nM for Bcl-xL, Bcl-2, Mcl-1, and Bfl-1, respectively.
PC-61017

BCL6 inhibitor 7

BCL6 inhibitor

BCL6 inhibitor 7 is a potent BCL6 protein-protein interaction inhibitor with Kd of 78 nM, exhibits an efficacy in cell-free and cellular PPI assays (ELISA IC50= 480 nM, M2H IC50= 8.6 uM).
PC-61016

BCL6 inhibitor 8c

BCL6 inhibitor

TP-021 (BCL6 inhibitor 8c) is a potent, in vivo-active BCL6 inhibitor with IC50 of 0.1 uM in ELISA assays.
PC-60951

BI-5273

BI-5273 is a negative control compound of BI-3802 and BI-3812, which are potent and efficacious BCL6 degrader and inhibitor, respectively.
PC-60950

BI-3812

BCL6 inhibitor

BI-3812 is a highly potent and efficacious BCL6 inhibitor that potently inhibits the interaction of the BTB/POZ domain of BCL6 with several co-repressors in vitro with IC50 of <3 nM.
PC-60949

BI-3802

BCL6 inhibitor

BI-3802 (BI3802) is a highly potent and efficacious BCL6 degrader that potently inhibits the interaction of the BTB/POZ domain of BCL6 with several co-repressors in vitro with IC50 of <3 nM.
PC-60941

DAN004

Bax inhibitor

DAN 004 is a small molecule Bax inhibitor that inhibits Bax/Bak oligomerization and prevents mitochondrial outer membrane permeabilization (MOMP) with IC50 of 0.7 uM.
PC-60940

MSN-125

Bax inhibitor

MSN-125 (MSN 125, MSN125) is a small molecule Bax inhibitor that inhibits Bax/Bak oligomerization and prevents mitochondrial outer membrane permeabilization (MOMP) with IC50 of 4 uM.
PC-60927

FX1

BCL6 inhibitor

FX1 (BCL6 inhibitor FX1) is a potent, specific BCL6 BTB domain inhibitor with Kd of 7 uM, binds with a greater affinity than the natural BCL6 ligand SMRT (Kd=30 uM).
PC-60926

BCL6 inhibitor 79-6

BCL6 inhibitor

BCL6 inhibitor 79-6 (Compound 79-6) is the first-generation, specific BCL6 BTB domain inhibitor with IC50 of 200 uM, Kd of 129 uM.
PC-60925

SMBA1

BAX activator

SMBA1 is a potent, and selective Bax agonist (Ki=43.3 nM) that induces conformational changes in Bax by blocking S184 phosphorylation.
PC-60924

CYD-2-11

Bax agonist

CYD-2-11 is a novel potent, selective Bax agonist that targets the structural pocket proximal to S184 in the C-terminal region of Bax (Ki=34.1 nM).

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