Catalog |
name |
Description |
price |
R-C-1667 |
TPEN CAS:16858-02-9 |
TPEN is a heavy metal chelator.Reacts with both Zn-proteome and Zn-metallothionein(MT)in LLC-PK1 cells;acts as an intracellular chelator of proteomic Zn2+. |
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R-C-1755 |
AZD5582 CAS:1258392-53-8 |
AZD5582 is an antagonist of the inhibitor of apoptosis proteins(IAPs),which binds to the BIR3 domains cIAP1,cIAP2,and XIAP with IC50s of 15,21,and 15 nM, respectively. |
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R-C-1759 |
GSK872 CAS:1346546-69-7 |
GSK872 is a receptor-interacting protein kinase-3(RIP3)inhibitor.GSK872 inhibits TNF-and virus-induced necrosis in 3T3-SA fibroblasts.It also inhibits necrosis induced by toll-like receptor 3(TLR3). |
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R-C-1813 |
MSDC-0160(CAY10415) CAS:146062-49-9 |
MSDC-0160 is a prototype mTOT-modulating insulin sensitizer being studied to treat diabetes and Alzheimer is disease. |
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R-C-1875 |
BAM7 CAS:331244-89-4 |
BAM7 is a direct and selective activator of proapoptotic BAX with an IC50 of 3.3μM. |
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R-C-1876 |
BTSA 1 CAS: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.It effectively promotes apoptosis in leukemia cell lines and patient samples while sparing healthy cells. |
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R-C-2251 |
Resibufogenin CAS:465-39-4 |
Resibufogenin(Bufogenin,Recibufogenin),a component of huachansu with anticancer effect,triggers necroptosis through upregulating receptor-interacting protein kinase 3(RIP3)and phosphorylating mixed lineage kinase domain-like protein at Ser358.Resibufogenin exerts cytotoxic effect by inducing reactive oxygen species(ROS)accumulation.Resibufogenin induces apoptosis and caspase-3 and caspase-8 activity. |
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R-C-1912 |
SM164 CAS:957135-43-2 |
SM-164 is a potent,non-peptide,cell-permeable antagonist of XIAP that targets both the BIR2 and BIR3 domains with IC50 of 1.39nM.SM-164 induces apoptosis and tumor regression. |
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R-C-1917 |
Pralsetinib (BLU-667) CAS:2097132-94-8 |
Pralsetinib(BLU-667,CS 3009,Gavreto)is a highly potent and selective RET (c-RET)inhibitor with an IC50 of 0.4 nM for WT RET.It also demonstrates potent activity(IC50 0.4 nmol/L)against common oncogenic RET alterations,including RET(M918T). |
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R-C-1924 |
S63845 CAS:1799633-27-4 |
S63845 is a potent and selective myeloid cell leukemia 1(MCL1)inhibitor with a Kd of 0.19nM for human MCL1. |
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