SINFACHEM LIMITED

SINFACHEM LIMITED
Country:  China (Mainland)
Business Type:  Lab/Research institutions
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Mr.Wang
Tel: 86-25-84683399
Fax:  86-25-84683112
City:  Nanjing
Street:  605, Phoenix Herui Plaza, No.389, South Taiping Road, Nanjing, China 210002
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Imatinib Mesylate

Imatinib Mesylate CAS NO.220127-57-1

  • Min.Order: 0 Metric Ton
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Keywords

  • Imatinib Mesylate
  • IHS
  • competitive price

Quick Details

  • ProName: Imatinib Mesylate
  • CasNo: 220127-57-1
  • Molecular Formula: C30H35N7O4S
  • Appearance: Off-White Solid
  • Application: Antineoplastic
  • DeliveryTime: 15 days after order confirmed
  • PackAge: 25kg/drum
  • Port: shanghai or hangzhou
  • ProductionCapacity: Metric Ton/Day
  • Purity: 98%
  • LimitNum: 0 Metric Ton

Superiority

1.Quality gurantee

2.Safe & Fast shipping since we have long reliable co-operated shiping companies

3.Prompty

4.Exfactory price, very competitive. 

5.Provide great service

Details

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.
Usage echinocandin antifungal, active against infections with Aspergillus and Candida, inhibits cell wall synthesis

 

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