Osimertinib
A third-generation EGFR inhibitor targeting specific mutations including T790M resistance in lung cancer.
Peso molecular
499,6050 g/mol
LogP
3,70
TPSA
87,60 Ų
Regla de cinco de Lipinski
Cumple
Áreas terapéuticas
Clases de fármacos
Mecanismo de acción
Third-generation irreversible EGFR TKI targeting T790M resistance mutation and activating mutations.
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Third-generation irreversible EGFR TKI targeting T790M resistance mutation and activating mutations.
Estructura 2D
Cite this structure
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SMILES
C=CC(=O)Nc1cc(Nc2nccc(-c3cn(C)c4ccccc34)n2)c(OC)cc1N(C)CCN(C)C
InChI
InChI=1S/C28H33N7O2/c1-7-27(36)30-22-16-23(26(37-6)17-25(22)34(4)15-14-33(2)3)32-28-29-13-12-21(31-28)20-18-35(5)24-11-9-8-10-19(20)24/h7-13,16-18H,1,14-15H2,2-6H3,(H,30,36)(H,29,31,32)
Molecular Formula
C28H33N7O2
HBD / HBA
2 / 7
Enlaces Rotables
10
Átomos Pesados
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.
Preguntas frecuentes
A third-generation EGFR inhibitor targeting specific mutations including T790M resistance in lung cancer.
Third-generation irreversible EGFR TKI targeting T790M resistance mutation and activating mutations.
Key pharmacokinetic parameters for Osimertinib: Half-life: 48 hours.
Yes, Osimertinib is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.
Related Drugs
References & Data Sources
- ChEMBL — European Bioinformatics Institute (EBI). CHEMBL3353410. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 71496458. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-28.
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