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| Product | Description | |
|---|---|---|
| AT-406 | AT-406 is a potent Smac mimetic and an antagonist of IAP (inhibitor of apoptosis protein via E3 ubiquitin ligase), binding to XIAP-BIR3 (with Ki of 66.4 nM), cIAP1-BIR3(with Ki of 1.9 nM) and cIAP2-BIR3 (with Ki of 5.1 nM), respectively. Synonyms: AT406; AT 406; SM-406; SM 406; SM406; ARRY-334543; ARRY 334543; ARRY334543. Grades: >98%. CAS No. 1071992-99-8. Molecular formula: C32H43N5O4. Mole weight: 561.71. |  |
| SM 406 | SM 406. Group: Biochemicals. Alternative Names: (5S, 8S, 10aR) -N- (Diphenylmethyl) decahydro-5-[[ (2S) -2- (methylamino) -1-oxopropyl]amino]-3- (3-methyl-1-oxobutyl) -6-oxo-pyrrolo[1, 2-a][1, 5]diazocine-8-carboxamide; AT 406. Grades: Highly Purified. CAS No. 1071992-99-8. Pack Sizes: 1mg. Molecular Formula: C32H43N5O4, Molecular Weight: 561.71. US Biological Life Sciences. |  Worldwide |
| Xevinapant | Xevinapant (AT-406) is a potent and orally bioavailable Smac mimetic and an antagonist of IAPs , and it binds to XIAP, cIAP1, and cIAP2 proteins with K i of 66.4, 1.9, and 5.1 nM, respectively. Uses: Scientific research. Group: Signaling pathways. Alternative Names: AT-406; Debio 1143; SM-406. CAS No. 1071992-99-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg. Product ID: HY-15454. |  |
| Xevinapant | Xevinapant Inhibitor. Uses: Scientific use. Product Category: T6763. CAS No. 1071992-99-8. |  |
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