Factory Ponatinib Pharmaceutical Grade Ponatinib

Product Details
Customization: Available
Powder: Yes
Customized: Negotiable
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Diamond Member Since 2025

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Registered Capital
1000000 RMB
Plant Area
101~500 square meters
  • Factory Ponatinib Pharmaceutical Grade Ponatinib
  • Factory Ponatinib Pharmaceutical Grade Ponatinib
  • Factory Ponatinib Pharmaceutical Grade Ponatinib
  • Factory Ponatinib Pharmaceutical Grade Ponatinib
  • Factory Ponatinib Pharmaceutical Grade Ponatinib
  • Factory Ponatinib Pharmaceutical Grade Ponatinib
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  • Overview
  • Product Description
  • Product Details
  • Application&Function
  • Specification
  • ABOUT US
Overview

Basic Info.

Model NO.
QS-Ponatinib
Certification
GMP, HSE, ISO 9001, USP, BP
Suitable for
Elderly, Children, Adult
State
Powder
Purity
>99%
Product Name
Ponatinib
CAS Number
943319-70-8
Molecular Formula
C29h27f3n6o
Molecular Weight
532.56 G/Mol
Appearance
White to off-White Powder
Identification
Retention Time Matches Reference Standard
Water Content
≤ 0.5%
Residual Solvents
Meets Ich Q3c Limits
Heavy Metals
≤ 20 Ppm
Melting Point
198°c - 202°c
Flow Rate
1.0 Ml/Min
Detection
UV @ 260 Nm
Injection Volume
10 µl
Column
C18 (e.g., Zorbax Sb-C18, 4.6 × 150 mm, 5
System Suitability
Rsd ≤ 2.0%
Transport Package
Negotiable
Specification
>99%
Trademark
QS
Origin
Xian
Production Capacity
300 Kg/Month

Product Description

Factory Ponatinib Pharmaceutical Grade Ponatinib
Factory Ponatinib Pharmaceutical Grade Ponatinib 
Product Description

Factory Ponatinib Pharmaceutical Grade PonatinibFactory Ponatinib Pharmaceutical Grade Ponatinib

Product Details

Factory Ponatinib Pharmaceutical Grade Ponatinib

Product Name Ponatinib 
Appearance White to off-white powder
MW 532.56 g/mol
MF C29H27F3N6O
CAS 943319-70-8
Ponatinib is an oral third-generation tyrosine kinase inhibitor (TKI) developed by Ariad Pharmaceuticals (now part of Takeda Pharmaceuticals), primarily used for the treatment of chronic myeloid leukemia (CML) and Philadelphia chromosome positive acute lymphoblastic leukemia (Ph+ALL). Its unique chemical structure can overcome common BCR-ABL1 mutation resistance, especially T315I mutation. This drug was approved by the US FDA in 2012 and is suitable for patients who are resistant or intolerant to other TKI drugs. It is an important treatment option for refractory leukemia.
Application&Function

Factory Ponatinib Pharmaceutical Grade PonatinibPonatinib effectively inhibits the activity of BCR-ABL1 fusion protein and its mutants (including T315I), blocks abnormal signal transduction, and thus inhibits the proliferation and survival of leukemia cells. In addition, it can also target and inhibit various kinases such as FGFR, PDGFR, VEGFR, etc., and has a broad-spectrum anti-tumor effect. Clinical studies have shown that Ponatinib can significantly improve the remission rate and prolong survival in drug-resistant CML and Ph+ALL patients, but caution should be exercised about its potential cardiovascular toxicity risks.
Factory Ponatinib Pharmaceutical Grade Ponatinib

Specification

Factory Ponatinib Pharmaceutical Grade PonatinibFactory Ponatinib Pharmaceutical Grade Ponatinib

Factory Ponatinib Pharmaceutical Grade PonatinibFactory Ponatinib Pharmaceutical Grade PonatinibFactory Ponatinib Pharmaceutical Grade PonatinibFactory Ponatinib Pharmaceutical Grade Ponatinib
ABOUT US

Factory Ponatinib Pharmaceutical Grade PonatinibFactory Ponatinib Pharmaceutical Grade PonatinibFactory Ponatinib Pharmaceutical Grade PonatinibFactory Ponatinib Pharmaceutical Grade Ponatinib

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