Pharmaceutical Intermediate Ponatinib

Product Details
Customization: Available
CAS No.: 57808-66-9
Formula: C29h27f3n6o
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  • Pharmaceutical Intermediate Ponatinib
  • Pharmaceutical Intermediate Ponatinib
  • Pharmaceutical Intermediate Ponatinib
  • Pharmaceutical Intermediate Ponatinib
  • Pharmaceutical Intermediate Ponatinib
  • Pharmaceutical Intermediate Ponatinib
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  • Overview
  • Product Description
  • Product Details
  • Application&Function
  • Specification
  • Packaging & Shipping
  • ABOUT US
Overview

Basic Info.

Model NO.
QS-L-Citrulline
EINECS
1308068-626-2
Packaging Material
Negotiable
Storage Method
Normal
Shelf Life
2 Years
Nutrient Composition
Rivaroxaban
Resource
Rivaroxaban
The content of active substances
99%
Product Name
Ponatinib
Name
Ponatinib Powder
Mf
C29h27f3n6o
MW
532.56 G/Mol
Density
1.292
Melting Point
>160
Appearance
Yellow Powder
Color
Yellow
Grade
Pharmaceutical Grade
Assay
HPLC 99%
Application
Anthelmintics
Specific
COA
Test Method
HPLC
Purity
≥99.0%
Refractive Index
1.622
Transport Package
Negotiable
Specification
99%
Trademark
QS
Origin
Xi′an Shaanxi
Production Capacity
500kg/Month

Product Description

Pharmaceutical Intermediate Ponatinib
Pharmaceutical Intermediate Ponatinib
Product Description
Pharmaceutical Intermediate PonatinibPharmaceutical Intermediate Ponatinib
Product Details
Pharmaceutical Intermediate Ponatinib
Product Name Ponatinib
Apperance Light yellow powder
CAS 943319-70-8
MF C29h27f3n6o
MW 532.56 
Ponatinib (CAS No. 57808-66-9) is a third-generation tyrosine kinase inhibitor (TKI) developed for the treatment of chronic myeloid leukemia (CML) and Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph+ ALL). It is marketed under the brand name Iclusig® and is distinguished by its unique ability to target BCR-ABL1 kinase mutations, including the T315I mutation, which confers resistance to earlier-generation TKIs.
Application&Function
Pharmaceutical Intermediate Ponatinib

Overcoming Resistance
Ponatinib's unique structure allows it to bypass common resistance mechanisms, including mutations that disrupt drug binding (e.g., T315I, F317L). Its high potency (IC50 of 0.37 nM for BCR-ABL1) ensures suppression of leukemic cell proliferation even at low concentrations.

Safety and Tolerability
While highly effective, Ponatinib carries a black box warning for vascular occlusion (arterial and venous thrombosis), heart failure, and hepatotoxicity. In clinical trials, 20-25% of patients experienced serious cardiovascular events, necessitating careful risk-benefit assessment. Common adverse effects include hypertension (30%), rash (25%), and pancreatitis (5%). Dose adjustments or discontinuation may be required for severe toxicity.

Role in Precision Medicine
Ponatinib exemplifies targeted cancer therapy, with efficacy guided by genetic testing for BCR-ABL1 mutations. It is reserved for patients with confirmed T315I mutations or those failing multiple TKIs.

Specification
Pharmaceutical Intermediate PonatinibPharmaceutical Intermediate PonatinibPharmaceutical Intermediate Ponatinib
Packaging & Shipping
Pharmaceutical Intermediate PonatinibPharmaceutical Intermediate PonatinibPharmaceutical Intermediate Ponatinib
ABOUT US
Pharmaceutical Intermediate PonatinibPharmaceutical Intermediate PonatinibPharmaceutical Intermediate PonatinibPharmaceutical Intermediate Ponatinib

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