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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T81148 | Smac-based peptide | ||
Smac-based peptide, a biologically active peptide derived from SMAC that interacts with the BIR3 domain, exhibits specific biological functions. | |||
T6763 | Xevinapant | ARRY-334543,SM-406,AT406,Debio-1143 | IAP |
Xevinapant (Debio-1143) is a potent Smac mimetic and an antagonist of IAP (inhibitor of apoptosis protein via E3 ubiquitin ligase), binding to XIAP-BIR3, cIAP1-BIR3 and cIAP2-BIR3 with Ki of 66.4 nM, 1.9 nM, and 5.1 nM, ... | |||
T3299 | Xevinapant hydrochloride | AT-406 HCl,SM-406 | Apoptosis , IAP |
Xevinapant hydrochloride (AT-406 HCl) , an orally active antagonist of multiple inhibitor of apoptosis proteins(IAP), inhibits progression of human ovarian Y binding to XIAP-BIR3, cIAP1-BIR3 and cIAP2-BIR3 with Ki of 66.... | |||
T20053 | Jasmacyclen | EC 226-501-6,NSC-6598,Verdyl acetate,Greenyl acetate,NS 6598,NSC 6598 | |
Jasmacyclen is a compound in which has an aroma. | |||
T35205 | Xylosmacin | ||
Xylosmacin is a biochemical. | |||
T2080 | LCL161 | IAP | |
LCL161, a SMAC mimetic, effectivity binds to and inhibits multiple IAPs (i.e. XIAP, c-IAP). | |||
T6007 | Birinapant | TL32711 | Apoptosis , IAP , HIV Protease |
Birinapant (TL32711) is a synthetic small molecule that is both a peptidomimetic of second mitochondrial-derived activator of caspases (SMAC) and inhibitor of IAP (Inhibitor of Apoptosis Protein) family proteins, with po... | |||
T12932L | SM-164 | Apoptosis , IAP | |
SM-164 binds to XIAP protein containing both the BIR2 and BIR3 domains (IC50: 1.39 nM). It acts as an extremely potent antagonist of XIAP. | |||
T26242 | SW IV-52 | SW-IV-52,SW IV52,SW IV 52,SWIV52 | |
SW IV-52 is an XIAP-inhibitor that acts as a second mitochondria-derived activator of caspases (SMAC) mimetic. | |||
T63969 | SM-433 | ||
SM-433 is a Smac mimetic and inhibitor of inhibitors of apoptosis (IAPs). SM-433 has a strong affinity for XIAP BIR3 protein (IC50 <1 μM). | |||
T64217 | SM-433 hydrochloride | ||
SM-433 hydrochlorid is a Smac mimetic, an inhibitor of inhibitory apoptosis proteins (IAPs). SM-433 hydrochlorid is able to bind XIAP BIR3 protein with a potent IC50 <1 μM. | |||
T15723 | LBW242 | Others | |
LBW242 is a 3-mer and Smac mimetic and is an effective and orally active proapoptotic IAP inhibitor. LBW242 has activity against multiple myeloma and potentiates TRAIL- and anticancer drug-mediated cell death of ovarian ... | |||
T75243 | SM-164 Hydrochloride | ||
SM-164 Hydrochloride, a cell-permeable Smac mimetic compound, exhibits high affinity for the XIAP protein, specifically targeting both the BIR2 and BIR3 domains, with an IC50 value of 1.39 nM. This action categorizes it ... | |||
T38857 | SBP-0636457 | SBI-0636457,SB1-0636457,SBP-0636457 | |
SBP-0636457 (SB1-0636457) is a SMAC mimetic and an inhibitor of inhibitor of apoptosis (IAP) proteins. It specifically binds to the BIR-domains of IAP proteins with a Ki value of 0.27 μM. SBP-0636457 holds potential for ... | |||
T12932 | SM-164 Hydrochloride (957135-43-2 free base) | SM-164 Hydrochloride | IAP |
SM-164 Hydrochloride is a cell-permeable Smac mimetic compound. SM-164 binds to XIAP protein containing both the BIR2 and BIR3 domains(IC50 value of 1.39 nM) and functions as an extremely potent antagonist of XIAP. | |||
T36201 | AZD5582 dihydrochloride | AZD 5582 dihydrochloride | |
Dimeric Smac mimetic; potent inhibitor of X-linked (XIAP) and cellular (cIAP) inhibitor of apoptosis protein (IC50 values are 15, 15 and 21 nM for XIAP, cIAP1 and cIAP2 respectively). Binds to the BIR3 domain of XIAP to ... | |||
T69323 | Dexamethasone sodium succinate | ||
Dexamethasone sodium succinate is the acetate salt form of dexamethasone, which is a synthetic glucocorticoid; it combines high anti-inflammatory effects with low mineralocorticoid activity. At high doses (e.g. 40 mg), i... | |||
T69200 | CGP74514A | ||
CGP74514A is a CDK1 inhibitor with potential anticancer activity. In U937 cells, CGP74514A - induced apoptosis (5 microM) became apparent within 4 hr and approached 100% by 24 hr. The pan- caspase inhibitor Boc-fmk and t... |