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Dasatinib Monohydrate API Active Pharmaceutical Ingredients CAS 863127-77-9

Dasatinib Monohydrate API Active Pharmaceutical Ingredients CAS 863127-77-9

Dasatinib Monohydrate API Active Pharmaceutical Ingredients CAS 863127-77-9

Product Details:

Place of Origin: China
Brand Name: Newlystar
Certification: GMP
Model Number: USP, BP

Payment & Shipping Terms:

Minimum Order Quantity: 25kg
Price: Negotiation
Packaging Details: 10kg, 25kg per drum
Delivery Time: 30days
Payment Terms: L/C, T/T
Supply Ability: Ten tons per month
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Detailed Product Description
Product: Dasatinib Monohydrate API CAS NO.: 863127-77-9
Purity: 99.0% Usage: Anti Cancer

Dasatinib Monohydrate API Active Pharmaceutical Ingredients CAS 863127-77-9

 

 

Dasatinib monohydrate API

CAS NO. 863127-77-9

Purity : 99.0%

 

Description :

Dasatinib is an oral dual BCR/ABL and Src family tyrosine kinase inhibitor approved for use in patients with chronic myelogenous leukemia (CML). The main targets of Dasatinib, are BCRABL, SRC, Ephrins and GFR.

 

Indication :

For the treatment of adults with chronic, accelerated, or myeloid or lymphoid blast phase chronic myeloid leukemia with resistance or intolerance to prior therapy. Also indicated for the treatment of adults with Philadelphia chromosome-positive acute lymphoblastic leukemia with resistance or intolerance to prior therapy.

 

Pharmacodynamics :

Dasatinib is an oral dual BCR/ABL and Src family tyrosine kinase inhibitor

 

Mechanism of action :

Dasatinib, at nanomolar concentrations, inhibits the following kinases: BCR-ABL, SRC family (SRC, LCK, YES, FYN), c-KIT, EPHA2, and PDGFRβ. Based on modeling studies, dasatinib is predicted to bind to multiple conformations of the ABL kinase. In vitro, dasatinib was active in leukemic cell lines representing variants of imatinib mesylate sensitive and resistant disease. Dasatinib inhibited the growth of chronic myeloid leukemia (CML) and acute lymphoblastic leukemia (ALL) cell lines overexpressing BCR-ABL. Under the conditions of the assays, dasatinib was able to overcome imatinib resistance resulting from BCR-ABL kinase domain mutations, activation of alternate signaling pathways involving the SRC family kinases (LYN, HCK), and multi-drug resistance gene overexpression.

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Newlystar (Ningbo) Medtech Co.,Ltd.

Contact Person: Luke Liu

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