Avapritinib CAS 1703793-34-3

Introduction:Basic information about Avapritinib CAS 1703793-34-3, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

Avapritinib Basic information

Product Name:Avapritinib
Synonyms:Avapritinib(BLU-285);BLU-285;CPD1212;Avapritinib;(1S)-1-(4-Fluorophenyl)-1-(2-{4-[6-(1-methyl-1H-pyrazol-4-yl)pyrrolo[2,1-f][1,2,4]triazin-4-yl]-1-piperazinyl}-5-pyrimidinyl)ethanamine;BLU-285 (Avapritinib);BLU-285;BLU 285;BLU285;CS-2474
CAS:1703793-34-3
MF:C26H27FN10
MW:498.56
EINECS:
Product Categories:API
Mol File:1703793-34-3.mol

Avapritinib Chemical Properties

density 1.42±0.1 g/cm3(Predicted)
storage temp. Store at -20°C
solubility DMSO:83.11(Max Conc. mg/mL);166.7(Max Conc. mM)
form A crystalline solid
pka6.96±0.10(Predicted)
color White to light yellow
InChIKeyDWYRIWUZIJHQKQ-JKXWNSIXNA-N
SMILESC1N(C2N=CC([C@@](N)(C3C=CC(F)=CC=3)C)=CN=2)CCN(C2C3=CC(C4C=NN(C)C=4)=CN3N=CN=2)C1 |&1:6,r|
CAS DataBase Reference1703793-34-3

Safety Information

Avapritinib Usage And Synthesis

DescriptionBLU-285 is a dual inhibitor of KIT receptor and platelet-derived growth factor receptor α (PDGFRα) tyrosine kinases with activating loop mutations (IC50s = 0.27 and 0.24 nM for KITD816V and PDGFRαD842V, respectively). It is >150-fold selective for KITD816V and PDGFRαD842V over a kinase panel at a concentration of 3 μM. BLU-285 also has activity against a panel of KIT and PDGFRα loop mutants identified in patients with gastrointestinal stromal tumors (GISTs; IC50s = <100 nM). It inhibits growth of cancer cell lines containing wild-type and mutant KIT and PDGFRα, demonstrating increased potency in cell lines expressing KIT and PDGFRα with activating loop mutations. BLU-285 (0.3-30 mg/kg) reduces tumor volume in a P815 KITD814Y mastocytoma allograft mouse model and a GIST patient-derived mouse xenograft model in a dose-dependent manner. Formulations containing BLU-285 have been used to treat KIT- and PDGFRα-driven malignancies.
UsesAvapritinib is a medication used for the treatment of tumors due to one specific rare mutation. Avapritinib is a potent, selective, and orally active KIT and PDGFRA activation loop mutant kinases inhibitor.
IndicationsAvapritinib is approved for the treatment of adult patients with unresectable or metastatic gastrointestinal mesenchymal stromal tumour (GIST) carrying platelet-derived growth factor receptor A (PDGFRA) exon 18 mutations, including the D842V mutation, as well as adult patients with advanced systemic mastocytosis (ASM).
Brand nameAyvakit
General DescriptionClass: receptor tyrosine kinase; Treatment: GIST, SM;Other name: BLU-285;Elimination half-life = 32–57 h;Protein binding = 98.8%
SynthesisBromide 213 was coupled with pyrazole boronate 214 to give triazone 215. Triazone 215 was converted to the corresponding chloride using phosphorus oxychloride and base in hot toluene. This chloride was smoothly coupled with piperazine 212 under basic conditions in dichloromethane to give avapritinib in high yield.
targetPrimary targets: PDGFRA, KIT
References[1] ERICA K. EVANS. A precision therapy against cancers driven by KIT/PDGFRA mutations[J]. Science Translational Medicine, 2017, 9 414. DOI: 10.1126/scitranslmed.aao1690

Avapritinib Preparation Products And Raw materials

AURAPTENE CAS 495-02-3
averantin CAS 5803-62-3
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