(S)-Diethyl 2-(4-(3-chloro-4-fluorophenylamino)-7-(tetrahydrofuran-3-yloxy)quinazolin-6-ylamino)-2-oxoethylphosphonate

98%

  • Product Code: 38142
  CAS:    618061-76-0
Molecular Weight: 552.92 g./mol Molecular Formula: C₂₄H₂₇ClFN₄O₆P
EC Number: MDL Number: MFCD19440885
Melting Point: Boiling Point:
Density: Storage Condition: 2-8°C, protected from light, stored in an inert gas
Product Description: This compound is primarily utilized in the development of targeted cancer therapies, particularly as an inhibitor of specific tyrosine kinases involved in tumor growth and proliferation. Its structure allows it to bind selectively to kinase domains, disrupting signaling pathways that promote cancer cell survival. Researchers explore its potential in treating cancers such as non-small cell lung cancer and breast cancer, where aberrant kinase activity is often observed. Additionally, it is studied for its efficacy in overcoming resistance to existing kinase inhibitors, offering a promising avenue for improved therapeutic outcomes. Its phosphonate group enhances cellular uptake and stability, making it a valuable candidate for further drug development and clinical trials.
Product Specification:
Test Specification
APPEARANCE White to light-yellow powder or crystals
PURITY 97.5-100
Infrared spectrum Conforms to Structure
NMR Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days ฿13,000.00
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0.250 10-20 days ฿20,600.00
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1.000 10-20 days ฿46,350.00
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(S)-Diethyl 2-(4-(3-chloro-4-fluorophenylamino)-7-(tetrahydrofuran-3-yloxy)quinazolin-6-ylamino)-2-oxoethylphosphonate
This compound is primarily utilized in the development of targeted cancer therapies, particularly as an inhibitor of specific tyrosine kinases involved in tumor growth and proliferation. Its structure allows it to bind selectively to kinase domains, disrupting signaling pathways that promote cancer cell survival. Researchers explore its potential in treating cancers such as non-small cell lung cancer and breast cancer, where aberrant kinase activity is often observed. Additionally, it is studied for its efficacy in overcoming resistance to existing kinase inhibitors, offering a promising avenue for improved therapeutic outcomes. Its phosphonate group enhances cellular uptake and stability, making it a valuable candidate for further drug development and clinical trials.
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