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S14161

Base Information
  • Chemical Name:S14161
  • CAS No.:883046-50-2
  • Molecular Formula:C17H14FNO4
  • Molecular Weight:315.301
  • Hs Code.:
  • Mol file:883046-50-2.mol
S14161

Synonyms:S14161;8-Ethoxy-2-(4-fluorophenyl)-3-nitro-2H-1-benzopyran

Suppliers and Price of S14161
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
  • Usbiological
  • S14161
  • 1mg
  • $ 297.00
  • TRC
  • S14161
  • 1mg
  • $ 45.00
  • TRC
  • S14161
  • 10mg
  • $ 340.00
  • Medical Isotopes, Inc.
  • S14161
  • 2.5 mg
  • $ 640.00
  • Cayman Chemical
  • S14161 ≥99%
  • 1mg
  • $ 60.00
  • Cayman Chemical
  • S14161 ≥99%
  • 5mg
  • $ 254.00
  • AK Scientific
  • 8-Ethoxy-2-(4-fluorophenyl)-3-nitro-2H-chromene
  • 5mg
  • $ 415.00
  • Adipogen Life Sciences
  • S14161 ≥99%(NMR)
  • 5 mg
  • $ 238.00
Total 5 raw suppliers
Chemical Property of S14161
Chemical Property:
  • Boiling Point:456.2±45.0 °C(Predicted) 
  • PSA:64.28000 
  • Density:1.34±0.1 g/cm3(Predicted) 
  • LogP:4.49890 
Purity/Quality:

98% *data from raw suppliers

S14161 *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Description D-Cyclins regulate the cell cycle by acting in a complex with cyclin dependent kinases (CDKs) to promote phosphorylation of the retinoblastoma protein and initiate cellular progression from the G1 to the S phase. Cell cycle deregulation in many cancers often results from altered cyclin D/CDK activity. S14161 is a small molecule inhibitor of cyclins D1-D3 expression that inhibits phosphoinositide 3-kinase activity and arrests cells at the G0/G1 phase in a dose-dependent manner (concentrations tested from 5-10 μM). S14161 induces apoptosis in myeloma and leukemia cell lines (IC50s < 10 μM) but is less toxic to normal hematopoietic cells (IC20 > 25 μM). In a mouse model of leukemia, S14161 delayed tumor growth by up to 90% compared to controls at a dose of 100 mg/kg/day.
  • Uses S14161 is a small-molecule inhibitor of D-cyclin transactivation that displays preclinical efficacy in myeloma and leukemia via phosphoinositide 3-kinase pathway. D-Cyclins regulate the cell cycle by acting in a complex with cyclin dependent kinases (CDKs) to promote phosphorylation of the retinoblastoma protein and initiate cellular progression from the G1 to the S phase. Cell cycle deregulation in many cancers often results from altered cyclin D/CDK activity. S14161 is a small molecule inhibitor of cyclins D1-D3 expression that inhibits phosphoinositide 3-kinase activity and arrests cells at the G0/G1 phase in a dose-dependent manner (concentrations tested from 5-10 μM). S14161 induces apoptosis in myeloma and leukemia cell lines (IC50s < 10 μM) but is less toxic to normal hematopoietic cells (IC20 > 25 μM). In a mouse model of leukemia, S14161 delayed tumor growth by up to 90% compared to controls at a dose of 100 mg/kg/day.[Cayman Chemical]
Technology Process of S14161

There total 2 articles about S14161 which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With triethylamine; L-proline; In toluene; at 90 ℃; for 24h; Reagent/catalyst; Solvent; Temperature; Time;
DOI:10.1016/j.bmcl.2013.03.097
Guidance literature:
With organocatalyst; In toluene; at 80 - 100 ℃;
DOI:10.1021/acs.jmedchem.5b00991
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