Imatinib Mesylate

98%

Reagent Code: #110422
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Alias Imatinib mesylate
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CAS Number 220127-57-1
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Properties Soluble in water (200 mg/ml), ethanol (~0.2 mg/ml), DMSO (200 mg/ml), DMF (~10 mg/ml), and methanol (sparingly).

science Other reagents with same CAS 220127-57-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 589.72 g/mol
Formula C₂₉H₃₁N₇OCH₄O₃S
badge Registry Numbers
MDL Number MFCD04307699
inventory_2 Storage & Handling
Storage 2~8℃

description Product Description

Imatinib Mesylate is primarily used in the treatment of certain types of cancer. It is highly effective in managing chronic myeloid leukemia (CML), where it targets the abnormal BCR-ABL protein produced by the Philadelphia chromosome, inhibiting the growth of cancerous cells. Additionally, it is used to treat gastrointestinal stromal tumors (GISTs) by blocking the activity of the KIT protein, which drives tumor growth. Imatinib Mesylate is also prescribed for patients with acute lymphoblastic leukemia (ALL) who have the Philadelphia chromosome mutation. Its ability to selectively inhibit tyrosine kinases makes it a cornerstone in targeted cancer therapy, significantly improving patient outcomes and survival rates.

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Test Parameter Specification
Purity (%) 97.5-100%

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿1,340.00
inventory 1g
10-20 days ฿660.00
inventory 25g
10-20 days ฿3,460.00
inventory 100g
10-20 days ฿13,280.00
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Imatinib Mesylate
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Imatinib Mesylate is primarily used in the treatment of certain types of cancer. It is highly effective in managing chronic myeloid leukemia (CML), where it targets the abnormal BCR-ABL protein produced by the Philadelphia chromosome, inhibiting the growth of cancerous cells. Additionally, it is used to treat gastrointestinal stromal tumors (GISTs) by blocking the activity of the KIT protein, which drives tumor growth. Imatinib Mesylate is also prescribed for patients with acute lymphoblastic leukemia (ALL) who have the Philadelphia chromosome mutation. Its ability to selectively inhibit tyrosine kinases makes it a cornerstone in targeted cancer therapy, significantly improving patient outcomes and survival rates.
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