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Home > Products >  BDTX-1535

BDTX-1535 CAS NO.2607829-38-7

  • Min.Order: 100 Gram
  • Payment Terms: L/C,T/T
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  • Product Details

Keywords

  • (2E)-N-[4-[(3-Chloro-2-fluorophenyl)amino]-7-[2-[(1R,5S)-3-methyl-3-azabicyclo[3.1.0]hex-1-yl]ethynyl]-6-quinazolinyl]-4-(4-morpholinyl)-2-butenamide
  • EGFR-IN-76
  • 2-Butenamide

Quick Details

  • ProName: BDTX-1535
  • CasNo: 2607829-38-7
  • Molecular Formula: C30H30ClFN6O2
  • Appearance: Yellow solid
  • Application: BDTX-1535 (EGFRIN-76) is a fourth-gene...
  • DeliveryTime: 2 months
  • PackAge: fiber can
  • Port: shanghai port
  • ProductionCapacity: 100 Kilogram/Year
  • Purity: 99%
  • Storage: store at 2-8℃
  • Transportation: air transport
  • LimitNum: 100 Gram
  • Related Substances: ≤0.1%
  • Residue on Ignition: ≤0.1%
  • Heavy Metal: ≤20ppm
  • Valid Period: 2 years

Superiority

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Details

English  named:BDTX1535

2-Butenamide,N-[4-[(3-chloro-2-fluorophenyl)amino]-7-[2-[(1R,5S) -3-methyl-3-Azabicyclo [3.1.0]hex-1-yl]ethynyl]-6-qui nazolinyl]-4-(4-morpholinyl)-,(2E)-
English synonyms :2-butenamide,N-[4-[(3Chemicalbook-chloro-2-fluorophenyl)amino]-7-[2-[(1R,5S) -3-methyl-3-Azabicyclo [3.1.0]hex-1-yl]e thynyl]-6-quinazolinyl]-4-(4-morpholinyl)-,(2E)-; BDTX-1535
CAS number 2607829-38-7
Molecular formula C30H30ClFN6O2
Molecular weight 561.05

Boiling point 730.0±60.0 °C(Predicted)
Density 1.42± 0.1g /cm3(Predicted)
Acidity coefficient (pKa)11.44±0.43(Predicted)
Form solid: color light yellow to yellow

Storage 0-4℃, can be stored for a few days to a few weeks; -20℃, can be stored for several months.
Soluble in DMSO and other organic solvents
Processing refers to MSDS
Transport conditions can be transported at room temperature.
Customs Code: 2934200090

BDTX-1535 (EGFRIN-76) is a fourth-generation, blood-brain barrier penetrating tyrosine kinase inhibitor (TKI). BDTX-1535 targets a wide range of oncogenic EGFR mutations in non-small cell lung cancer (NSCLC), including classical and non-classical drive mutations and C797S mutations. In addition, BDTX-1535 also inhibits EGFR extracellular domain mutations common in glioblastoma (GBM).

 

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