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152460-10-1 N-(5-Amino-2-methylphenyl)-4-(3-pyridyl)-2-pyrimidineamine Imatinib intermediate
N-(5-AMINO-2-METHYLPHENYL)-4-(3-PYRIDYL)-2-PYRIMIDINEAMINE(152460-10-1)
Information
Imatinib intermediate.
Imatinib is the first-generation tyrosine kinase inhibitor and a milestone drug in the history of the treatment of chronic myeloid leukemia (CML). It was launched by Novartis in 2001 and is a successful model of targeted therapy. It only kills BCR-ABL contained in myeloid cells, prevents cell proliferation and tumor formation, but has no effect on normal cells. It can also inhibit PDGF-mediated tumors, including glioma and prostate cancer.
Quality
Advanced technology
Supper quality
Effective & safety package
Service
Professional and timely afte-sale service(replied within 12h)
COMPANY INFORMATION
Jinan Kangcheng Pharmaceutical Technology Co., Ltd.
Add:Jinan Area,China(Shandong) Pilot Free Trade Zone,China
The company focuses on the development and transfer of pharmaceutical technology. It is a modern enterprise integrating technology development, transfer and sales of APIs, pharmaceutical intermediates, and nutraceutical raw materials.
The company adheres to the principle of integrity and innovation, and provides customers with professional products and advanced technical services.
N-(5-AMINO-2-METHYLPHENYL)-4-(3-PYRIDYL)-2-PYRIMIDINEAMINE |
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Product information |
English Name:N-(5-Amino-2-methylphenyl)-4-(3-pyridyl)-2-pyrimidineamine |
English Alias:4-Methyl-N'-[4-(pyridin-3-yl)pyrimidin-2-yl]benzene-1,3-diamine; N-(5-amino-2-methylphenyl)-4-(3-pyrdyl)-2-pydimidineamine; N-(5-amino-2-methylphenyl)-4-(3-pyridyl)-2-pyrimidine-amine; N-(5-amino-2-methylphenl)-4-(3-pyridyl)-2-pyrimidine-amine |
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Chinese Name:伊马胺 |
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Chinese Alias:N-(5-氨基-2-甲基苯基)-4-(3-吡啶基)-2-氨基嘧啶; N-(5-氨基-2-甲基苯基l)-4-(3-吡啶)-2-嘧啶胺; |
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CAS号:152460-10-1 |
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Forla:C16H15N5 |
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Molecular weight:277.32 |
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Appearance:White to light yellow power |
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Purity:98.0% |
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Use&Pharmacology |
Imatinib intermediate. Imatinib is the first-generation tyrosine kinase inhibitor and a milestone drug in the history of the treatment of chronic myeloid leukemia (CML). It was launched by Novartis in 2001 and is a successful model of targeted therapy. It only kills BCR-ABL contained in myeloid cells, prevents cell proliferation and tumor formation, but has no effect on normal cells. It can also inhibit PDGF-mediated tumors, including glioma and prostate cancer. In the 1980s, scientific research showed that the granulocytes of most patients with chronic myelogenous leukemia had two chromosomes transposed, resulting in the fusion kinase BCR-ABL, which led to the continuous activation of the kinase activity, resulting in uncontrolled cell proliferation -Blood cancer. On this basis, Dr. Druker, a biologist at Oregon University of Health Sciences in the United States, proposed the hypothesis of using BCR-ABL as a drug target, and proposed the development of kinase inhibitors of this target to treat chronic myeloid leukemia. The second is the screening and optimization of the lead: Then, Druker and Novartis chemist Nick Lydon cooperated to select small molecule inhibitors that inhibit BCR-ABL kinase from the compound library and develop imatinib after optimization. Third, the results of preclinical research and clinical trials have shown that imatinib is safe and effective. The vast majority of chronic myelogen patients get complete hematological relief, and the side effects are much less than that of cytotoxic anti-tumor drugs. |
Package&Storage |
Package:1kg/bag, 10kg/drum, 25kg/drum (on request) |
Storage&Validity:Cool, shading, dry and sealed/2years |
CAS NO:29407-84-9
CAS NO:152460-10-1
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