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Osimertinib

CHEMBL3353410 Phase 4 Disetujui Small molecule
Half-Life
48 hours
Bioavailability
—
Protein Binding
—
Molecular Weight
499.6 g/mol
LogP
3.7
Phase
4

A third-generation EGFR inhibitor targeting specific mutations including T790M resistance in lung cancer.

Berat Molekul

499,6050 g/mol

LogP

3,70

TPSA

87,60 Ų

Lipinski RO5

Lulus

Area Terapeutik

Ovarian Cancer Pancreatic Cancer Bladder Cancer Thyroid Cancer Non-Small Cell Lung Cancer Melanoma Oncology Lymphoma Breast Cancer Prostate Cancer Colorectal Cancer

Kelas Obat

L — L - Antineoplastic and Immunomodulating Agents

Mekanisme Kerja

Third-generation irreversible EGFR TKI targeting T790M resistance mutation and activating mutations.

Pharmacokinetics (PK)

Half-Life 48 hours

Pharmacodynamics (PD)

Mekanisme

Third-generation irreversible EGFR TKI targeting T790M resistance mutation and activating mutations.

Struktur 2D

SVG PNG

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

                    

                    
                    

                        
Ikatan yang Dapat Dirotasi

                        
10

                    

                    
                    
                    

                        
Atom Berat

                        
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.

    



                
            


            
            
            

                
Pertanyaan yang Sering Diajukan

                

                    
                    

                        
                        

                            
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.

                        

                    

                

            

            

            
            
            

                
                
                    ADME Journey →
                
                
                
            

            

            
            
            

                
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{# References & Data Sources section for drug detail pages.
   Renders standard pharmacological database links plus the drug's data_sources field. #}


    
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.




        


        
        
    


    



    
Penyangkalan Medis

    

        This content is for educational and informational purposes only. It is not a substitute for professional medical advice, diagnosis, or treatment. Always consult a qualified healthcare provider before making medication decisions.
    

    

        Data sources:
        ChEMBL,
        PubChem,
        DailyMed.