Avapritinib
A potent and selective kinase inhibitor targeting KIT and PDGFRA mutations, used for unresectable or metastatic gastrointestinal stromal tumors. It offers a treatment option for a form of GIST that did not previously respond to available therapies.
Khối lượng phân tử
498,6000 g/mol
LogP
1,90
TPSA
106,00 Ų
Lipinski RO5
Đạt
Lĩnh vực điều trị
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Cấu trúc 2D
Cite this structure
Embed this structure
SMILES
Cn1cc(-c2cc3c(N4CCN(c5ncc([C@@](C)(N)c6ccc(F)cc6)cn5)CC4)ncnn3c2)cn1
InChI
InChI=1S/C26H27FN10/c1-26(28,20-3-5-22(27)6-4-20)21-13-29-25(30-14-21)36-9-7-35(8-10-36)24-23-11-18(16-37(23)33-17-31-24)19-12-32-34(2)15-19/h3-6,11-17H,7-10,28H2,1-2H3/t26-/m0/s1
Molecular Formula
C26H27FN10
HBD / HBA
1 / 9
Liên kết có thể quay
5
Nguyên tử nặng
37
No targets recorded
Target interaction data is not yet available for this drug.
No interactions recorded
Drug interaction data is not yet available for this compound.
No side effects recorded
Side effect data is not yet available for this drug.
Câu hỏi thường gặp
A potent and selective kinase inhibitor targeting KIT and PDGFRA mutations, used for unresectable or metastatic gastrointestinal stromal tumors. It offers a treatment option for a form of GIST that did not previously respond to available therapies.
Yes, Avapritinib is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.
References & Data Sources
- ChEMBL — European Bioinformatics Institute (EBI). CHEMBL4204794. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 118023034. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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