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Befotertinib

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Befotertinib Basic information

Product Name:
Befotertinib
Synonyms:
  • N-(2-((2-(dimethylamino)ethyl)(methyl)amino)-4-methoxy-5-((4-(1-(2,2,2-trifluoroethyl)-1H-indol-3-yl)pyrimidin-2-yl)amino)phenyl)acrylamide
  • 2-Propenamide, N-[2-[[2-(dimethylamino)ethyl]methylamino]-4-methoxy-5-[[4-[1-(2,2,2-trifluoroethyl)-1H-indol-3-yl]-2-pyrimidinyl]amino]phenyl]-
  • Befotertinib
  • CPD0557
  • lung,Epidermal growth factor receptor,D0316,D 0316,ErbB-1,Inhibitor,HER1,inhibit,cancer,EGFR,kinase,tyrosine,non-small,NSCLC
  • Befotertinib, 10 mM in DMSO
  • Befotertinib (D-0316)
CAS:
1835667-63-4
MF:
C29H32F3N7O2
MW:
567.61
Mol File:
1835667-63-4.mol
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Befotertinib Chemical Properties

Density 
1.26±0.1 g/cm3(Predicted)
storage temp. 
Store at -20°C
solubility 
DMSO : 62.5 mg/mL (110.11 mM; ultrasonic and warming and heat to 60°C)
pka
12.68±0.70(Predicted)
form 
Solid
color 
Light yellow to yellow
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Befotertinib Usage And Synthesis

Uses

Befotertinib (D-0316) is the third-generation EGFR tyrosine kinase inhibitor. Befotertinib can be used for the research of EGFR T790M-positive non-small cell lung cancer (NSCLC)[1].

References

[1] Nagasaka M, et, al. Beyond Osimertinib: The Development of Third-Generation EGFR Tyrosine Kinase Inhibitors For Advanced EGFR+ NSCLC. J Thorac Oncol. 2021 May;16(5):740-763. DOI:10.1016/j.jtho.2020.11.028

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