Overview of Ponatinib powder:
Ponatinib powder is an anticancer drug. It was approved by FDA in December, 2012, and used to treat adult chronic myeloid leukemia (CML) and Philadelphia chromosome positive (Ph+) acute lymphoblastic leukemia (ALL).
Ponatinib powder is a yellow powder, which is soluble in DMSO (up to 50mg/ml) or ethanol (up to 25mg/ml). It has good stability and can be stored in DMSO or ethanol solution at-20 for up to 3 months.

| Product name | Ponatinib powder |
| CAS | 943319-70-8 |
| Molecular formula | C29H27F3N6O |
| Molecular weight | 532.56 |
| EINECS Number | 1308068-626-2 |
| Melting point | >175°C (dec.) |
| Acidity coefficient (pKa) | 12.99±0.70(Predicted) |
| Solubility | Soluble in DMSO (up to 50mg/ml) or ethanol (up to 25mg/ml). |
| Appearance | Yellow powder |
| Storage condition | -20°C |
| Density | 1.3 |
What is Ponatinib powder?
Ponatinib powder is an anticancer drug. It was approved by FDA in December, 2012, and used to treat adult chronic myeloid leukemia (CML) and Philadelphia chromosome positive (Ph+) acute lymphoblastic leukemia (ALL).

What kind of patients can Ponatinib treat?
Ponatinib is mainly used to treat patients who have no response to dasatinib or nilotinib, or patients who cannot tolerate dasatinib or nilotinib, and patients who are not suitable for subsequent treatment with imatinib.
It can also be used to treat patients with gene mutation ("T315I mutation"), which makes patients resistant to imatinib, dasatinib or nilotinib. Ponatinib is also used to treat CML and Ph+ALL in adults who have not been treated with other TKIs.
Ponatinib is the only effective drug for mutation of Bcr-Abl kinase T315I.
Ponatinib is the only effective drug for mutation of Bcr-Abl kinase T315I. Ponatinib was approved in July 2013 in the European Union through a centralized approval process. It is the third generation of multi-target tyrosine kinase inhibitors. The typical drugs of multi-target tyrosine kinase inhibitors are sunitinib, imatinib, sorafenib and vataranib.
On November 22, 2013, the European Medicines Agency (EMA) released a message that the Committee for Medicines for People (CHMP) proposed to update the use of Ponatinib to help patients minimize the risk of blood clots blocking arteries or veins.

product Specification
| Item | Specification | Results | |
|
Appearance |
Light yellow solid powder | Complies | |
| Identification | By IR | Complies | |
|
|
By HPLC | Complies | |
|
Loss on drying(%) |
≤1.00% | 0.85% | |
| Heavy Metals | ≤20ppm | Complies | |
| Residue on Ignition | ≤0.20% | 0.09% | |
| Related Substance | Any single impurity: ≤0.50% | 0.10% | |
| Total Impurities: ≤1.00% | 0.30% | ||
| Assay(HPLC basis on drying) | 98.0%~102.0% | 99.25% | |
| Conclusion: The test results are conformed to the in-house specification | |||
What is the therapeutic effect of Ponatinib?
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Attention: It should be noted that this product is not intended for the diagnosis, treatment, cure, or prevention of any disease. Please consult your doctor and learn about available research before use. Please do not use without authorization. This compound can only be used for research purposes. The US Food and Drug Administration has not evaluated these claims.
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