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Bcl2

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Bcl2

Chemical Structure Cat. No. Product Name CAS No.
VU661013 Chemical Structure
 BCP31022 VU661013 2131184-57-9
VU661013 is a potent and selective MCL-1 inhibitor.
TW-37 Chemical Structure
 BCP27702 TW-37 877877-35-5
TW-37 is a potent Bcl-2 inhibitor with Ki values of 260, 290 and 1110 nM for Mcl-1, Bcl-2 and Bcl-xL, respectively.
AZD-5991 S-enantiomer Chemical Structure
 BCP30973 AZD-5991 S-enantiomer 2143061-82-7
AZD-5991 S-enantiomer is the less active enantiomer of AZD-5991.
AZD5991 Chemical Structure
 BCP30972 AZD5991 2143061-81-6
AZD-5991 is a potent and selective Mcl-1 inhibitor with an IC50 of 0.7 nM in FRET assay and a Kd of 0.17 nM in surface plasmon resonance (SPR) assay.
BTSA 1 Chemical Structure
 BCP30923 BTSA 1 314761-14-3
BTSA1 is a pharmacologically optimized BAX activator that binds with high affinity and specificity to the N-terminal activation site and induces conformational changes to BAX leading to BAX-mediated apoptosis.
Bax channel blocker Chemical Structure
 BCP30816 Bax channel blocker 335165-68-9
Bax channel blocker is a direct allosteric inhibitor of BAX.
Ornidazole Levo- Chemical Structure
 BCP12975 Ornidazole Levo- 166734-83-4
Ornidazole Levo- is the levo-isomer of Ornidazole. Ornidazole is a 5-nitroimidazole derivative with antiprotozoal and antibacterial properties against anaerobic bacteria.
Glycocholic acid sodium salt hydrate Chemical Structure
 BCP17746 Glycocholic acid sodium salt hydrate 338950-81-5
Glycocholic acid is a bile acid with anticancer activity, targeting against pump resistance-related and non-pump resistance-related pathways.
Glycocholic acid Chemical Structure
 BCP13102 Glycocholic acid 475-31-0
Glycocholic acid is a bile acid with anticancer activity, targeting against pump resistance-related and non-pump resistance-related pathways.
AMG176 Chemical Structure
 BCP25146 AMG176 1883727-34-1
AMG-176 is an inhibitor of induced myeloid leukemia cell differentiation protein MCL-1 (myeloid cell leukemia-1), with potential pro-apoptotic and antineoplastic activities.
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