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Home > Products >  Imatinib mesylate

Imatinib mesylate CAS NO.220127-57-1

  • Min.Order: 1 Kilogram
  • Payment Terms: L/C,T/T,Other
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Quick Details

  • ProName: Imatinib mesylate
  • CasNo: 220127-57-1
  • Molecular Formula: C30H35N7O4S
  • Appearance: Off-white solid
  • Application: A tyrosine kinase inhibitor. Highly sp...
  • DeliveryTime: 15 days after order confirmed
  • PackAge: 25kg/drum;200kg/drum as per your reque...
  • Port: Shanghai, Ningbo, Tianjin, etc
  • ProductionCapacity: 100 Metric Ton/Month
  • Purity: 99%
  • Storage: Stored in cool, dry and ventilation pl...
  • Transportation: by courier door to door or by sea
  • LimitNum: 1 Kilogram

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Superior quality, moderate price & quick delivery.

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Imatinib mesylate Chemical Properties
mp  214-224°C
storage temp.  -20°C Freezer
CAS DataBase Reference 220127-57-1(CAS DataBase Reference)
 
Safety Information
Hazardous Substances Data 220127-57-1(Hazardous Substances Data)
MSDS Information
 
 
Imatinib mesylate Usage And Synthesis
a small-molecule inhibitor Imatinib mesylate (also called Gleevec) is a small-molecule inhibitor of the fusion protein Bcr-Abl, the causal agent in chronic myelogenous leukemia.
As an inhibitor of PDGFR, imatinib mesylate appears to have utility in the treatment of a variety of dermatological diseases. Imatinib has been reported to be an effective treatment for FIP1L1-PDGFRalpha+ mast cell disease, hypereosinophilic syndrome, and dermatofibrosarcoma protuberans.
Chemical Properties Off-White Solid
Usage A tyrosine kinase inhibitor. Highly specific for BCR-ABL, the enzyme associated with chronic myelogenous leukemia (CML) and certain forms of acute lymphoblastic leukemia (ALL)
Usage Imatinib Mesylate is orally bioavailability mesylate salt of Imatinib, which is a multi-target inhibitor of v-Abl, c-Kit and PDGFR with IC50 of 0.6 μM, 0.1 μM and 0.1 μM, respectively. Imatinib also known as Gleevec, Glivec, CGP-57148B, STI-571 & Imatinib
Usage Imatinib Mesylate (STI571) is an orally bioavailability mesylate salt of Imatinib, which is a multi-target inhibitor of v-Abl, c-Kit and PDGFR with IC50 of 0.6 μM, 0.1 μM and 0.1 μM, respectively.

 

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