Ilginatinib maleate (NS-018 maleate)

≥98%

Reagent Code: #108588
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CAS Number 1354799-87-3

science Other reagents with same CAS 1354799-87-3

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scatter_plot Molecular Information
Weight 505.50 g/mol
Formula C₂₅H₂₄FN₇O₄
inventory_2 Storage & Handling
Storage -20°C, airtight, dry

description Product Description

Ilginatinib maleate (NS-018 maleate) is a selective Janus kinase 2 (JAK2) inhibitor primarily investigated for the treatment of myelofibrosis, a myeloproliferative neoplasm characterized by bone marrow fibrosis and disrupted blood cell production. It targets the JAK-STAT signaling pathway, which is frequently dysregulated due to JAK2 mutations (e.g., V617F) in such disorders. By inhibiting JAK2, it reduces splenomegaly, constitutional symptoms like fatigue and anemia, and may improve overall survival. Clinical trials have also explored its efficacy in other JAK2-mutated hematologic malignancies, such as polycythemia vera and essential thrombocythemia. As an oral targeted therapy, it represents a promising option for patients with limited alternatives, though it remains in investigational stages.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿40,176.00

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Ilginatinib maleate (NS-018 maleate)
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Ilginatinib maleate (NS-018 maleate) is a selective Janus kinase 2 (JAK2) inhibitor primarily investigated for the treatment of myelofibrosis, a myeloproliferative neoplasm characterized by bone marrow fibrosis and disrupted blood cell production. It targets the JAK-STAT signaling pathway, which is frequently dysregulated due to JAK2 mutations (e.g., V617F) in such disorders. By inhibiting JAK2, it reduces splenomegaly, constitutional symptoms like fatigue and anemia, and may improve overall survival. Cl

Ilginatinib maleate (NS-018 maleate) is a selective Janus kinase 2 (JAK2) inhibitor primarily investigated for the treatment of myelofibrosis, a myeloproliferative neoplasm characterized by bone marrow fibrosis and disrupted blood cell production. It targets the JAK-STAT signaling pathway, which is frequently dysregulated due to JAK2 mutations (e.g., V617F) in such disorders. By inhibiting JAK2, it reduces splenomegaly, constitutional symptoms like fatigue and anemia, and may improve overall survival. Clinical trials have also explored its efficacy in other JAK2-mutated hematologic malignancies, such as polycythemia vera and essential thrombocythemia. As an oral targeted therapy, it represents a promising option for patients with limited alternatives, though it remains in investigational stages.

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