Product name
|
Dasatinib
|
Molecular Formula
|
C22H28CIN7O3S
|
Molecular Weight
|
506.02
|
CAS No.
|
302962-49-8
|
Quality Standard
|
USP26, EP,
medical grade
|
Appearance
|
White powder
|
ITEMS
|
SPECIFICATION
|
RESULTS
|
IDENTIFICATION
|
POSITIVE REACTION
|
CONFORMS
|
Water
|
≤1.5%
|
0.9%
|
LOSS ON DRYING
|
≤0.1%
|
0.03%
|
RESIDUE ON IGNITION
|
≤0.1%
|
0.02%
|
CHROMATOGRAPHIC PURITY
|
RANITIDINE RELATED COMPOUND B≤0.5%
ANY OTHER IMPURITY≤0.3%
THE SUM OF ALL IMPURITIES≤1.0%
|
CONFORMS
CONFORMS
CONFORMS
|
ORGANIC VOLATILE IMPURITIES
|
AS STIPULATED
|
CONFORMS
|
ASSAY
(ON DRY SUBSTANCE)
|
98.0%~102.0%
|
99.8%
|
CONCLUSION
|
CONFORMS TO in house
|
Function of Dasatinib
Dasatinib (DASA tin IB), used for all treatment stages (chronic
phase, accelerated phase) Stage, lymphoid cell blast crisis and myeloid blast
crisis) adult patients. At the same time, the FDA also approved Dasatinib
through normal procedures to treat Philadelphia chromosome-positive acute lymphoblastic
leukemia adult patients who are resistant or intolerant to other therapies.
Dasatinib inhibits BCR-ABL kinase and SRC family kinases
as well as many other selective oncogenic kinases, including c-KIT, ephrin
(EPH) receptor kinase and PDGFβ receptor. Dasatinib is a potent, subnanomolar
BCR-ABL kinase inhibitor with a strong activity at a concentration of 0.6 to
0.8 nmol. It can be combined with the inactive and active configurations of the
BCR-ABL enzyme.
In vitro studies, dasatinib is active in
leukemia cell lines expressing various imatinib-sensitive and drug-resistant
diseases. The results of these non-clinical studies indicate that dasatinib can
overcome imatinib resistance caused by: BCR-ABL overexpression, BCR-ABL kinase
region mutations, kinases including SRC family kinases (LYN, HCK) in
Over-expression of other signaling pathways within, as well as multidrug
resistance genes. In addition, dasatinib can inhibit SRC family kinases at this
nanomolar concentration
In an in vivo experiment conducted using
the murine CML model alone, dasatinib prevented the progression of chronic
phase CML to the acute phase, while prolonging tumor-bearing mice (derived from
patient CML cell lines growing in different locations, including the central
Nervous system)