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AT-406(AT406)

Base Information
  • Chemical Name:AT-406(AT406)
  • CAS No.:1071992-99-8
  • Molecular Formula:C32H43N5O4
  • Molecular Weight:561.71
  • Hs Code.:29339900
  • Mol file:1071992-99-8.mol
AT-406(AT406)

Synonyms:QCR-136;SM 406;AT406 (SM-406);AT-406;

Suppliers and Price of AT-406(AT406)
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • Medical Isotopes, Inc.
  • SM406
  • 50 mg
  • $ 2025.00
  • Medical Isotopes, Inc.
  • SM406
  • 5 mg
  • $ 750.00
  • Medical Isotopes, Inc.
  • SM406
  • 1 mg
  • $ 610.00
  • DC Chemicals
  • AT-406(Xevinapant) >98%
  • 100 mg
  • $ 550.00
  • Crysdot
  • AT406(SM-406,ARRY-334543) 98+%
  • 10mg
  • $ 119.00
  • Crysdot
  • AT406(SM-406,ARRY-334543) 98+%
  • 25mg
  • $ 266.00
  • Crysdot
  • AT406(SM-406,ARRY-334543) 98+%
  • 5mg
  • $ 77.00
  • Crysdot
  • AT406(SM-406,ARRY-334543) 98+%
  • 50mg
  • $ 406.00
  • Chemenu
  • AT406(SM-406,ARRY-334543) 98%
  • 50mg
  • $ 380.00
  • Cayman Chemical
  • AT-406 ≥95%
  • 10mg
  • $ 300.00
Total 35 raw suppliers
Chemical Property of AT-406(AT406)
Chemical Property:
  • Boiling Point:840.6±65.0 °C(Predicted) 
  • PKA:13.65±0.40(Predicted) 
  • PSA:117.83000 
  • Density:1.21 
  • LogP:4.57020 
  • Solubility.:≥27.65 mg/mL in DMSO; insoluble in H2O; ≥27 mg/mL in EtOH 
Purity/Quality:

99%, *data from raw suppliers

SM406 *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Description AT-406 is an orally bioavailable Smac/DIABLO mimetic and antagonist of the inhibitor of apoptosis proteins (IAPs). It binds to XIAP, cIAP1, and cIAP2 proteins with Ki values of 66.4, 1.9, and 5.1 nM, respectively. It has been shown to inhibit cancer cell growth in various human cancer cell lines and to induce apoptosis in xenograft tumors in mice.
  • Uses AT-406 is a potent IAP (inhibitor of apoptosis protein) inhibitor of XIAP, cIAP1, and cIAP2 with Ki of 66.4 nM, 1.9 nM, and 5.1 nM, respectively. SM 406 is a potent and orally active antagonist of multiple inhibitor of apoptosis proteins (IAPs).
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