
CAS 1703793-34-3
:Avapritinib
Description:
Avapritinib is a small molecule tyrosine kinase inhibitor primarily used in the treatment of certain types of cancers, particularly those associated with mutations in the KIT gene, such as gastrointestinal stromal tumors (GISTs). It selectively inhibits the activity of mutant forms of the KIT protein, which plays a crucial role in cell signaling pathways that regulate cell growth and survival. Avapritinib is characterized by its high specificity for the mutant forms of the target, which helps minimize off-target effects and enhances its therapeutic efficacy. The compound is administered orally and has a favorable pharmacokinetic profile, allowing for effective systemic exposure. Its development was driven by the need for targeted therapies in oncology, and it has been evaluated in clinical trials for its safety and efficacy. As with many targeted therapies, potential side effects may include hematologic abnormalities, gastrointestinal disturbances, and fatigue, necessitating careful monitoring during treatment. Overall, Avapritinib represents a significant advancement in personalized cancer therapy.
- (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
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Found 6 products.
Ref: IN-DA01DQAS
2gTo inquire5gTo inquire1mg105.00€2mg124.00€5mg148.00€10mg177.00€25mg190.00€50mg218.00€100mg347.00€250mg555.00€Avapritinib
CAS:Avapritinib (BLU-285) is a selective, highly potent, and orally active inhibitor of KIT and PDGFRA activation loop mutant kinases.Cost-effective and quality-assured.Formula:C26H27FN10Purity:96.59% - 99.7%Color and Shape:SolidMolecular weight:498.56BLU 285
CAS:<p>Inhibitor of exon 17 mutant KIT and PDGFRA D842V</p>Formula:C26H27FN10Purity:Min. 95%Color and Shape:PowderMolecular weight:498.56 g/mol




