TAK-659
10mM in H2O
- Product Code: 239390
CAS:
1952251-28-3
| Molecular Weight: | 380.85 g./mol | Molecular Formula: | C₁₇H₂₁FN₆·HCl |
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| Density: | Storage Condition: | -20°C |
Product Description:
TAK-659 is a potent and selective inhibitor of spleen tyrosine kinase (SYK), which plays a key role in signaling pathways involved in immune cell activation and survival. It is primarily investigated for its therapeutic potential in hematologic malignancies, particularly B-cell lymphomas and leukemias. By blocking SYK activity, TAK-659 disrupts downstream signaling pathways that promote tumor cell proliferation and survival, leading to reduced cancer cell growth and induction of apoptosis.
The compound has shown promising activity in clinical trials for relapsed or refractory non-Hodgkin lymphoma, including diffuse large B-cell lymphoma (DLBCL) and follicular lymphoma. Its oral bioavailability and targeted mechanism make it a favorable candidate for combination therapies with other agents such as rituximab or BTK inhibitors. Additionally, TAK-659 is being explored in autoimmune and inflammatory conditions where SYK-mediated signaling contributes to disease pathology, though oncology remains its primary focus.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 1ml | 10-20 days | ฿6,200.00 |
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TAK-659
TAK-659 is a potent and selective inhibitor of spleen tyrosine kinase (SYK), which plays a key role in signaling pathways involved in immune cell activation and survival. It is primarily investigated for its therapeutic potential in hematologic malignancies, particularly B-cell lymphomas and leukemias. By blocking SYK activity, TAK-659 disrupts downstream signaling pathways that promote tumor cell proliferation and survival, leading to reduced cancer cell growth and induction of apoptosis.
The compound has shown promising activity in clinical trials for relapsed or refractory non-Hodgkin lymphoma, including diffuse large B-cell lymphoma (DLBCL) and follicular lymphoma. Its oral bioavailability and targeted mechanism make it a favorable candidate for combination therapies with other agents such as rituximab or BTK inhibitors. Additionally, TAK-659 is being explored in autoimmune and inflammatory conditions where SYK-mediated signaling contributes to disease pathology, though oncology remains its primary focus.
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