Erlotinib

CHEMBL553 Phase 4 Disetujui Small molecule
Half-Life
36 hours
Bioavailability
Protein Binding
Molecular Weight
393.4 g/mol
LogP
3.3
Phase
4

This oral targeted therapy blocks the EGFR protein that drives the growth of cancer cells in certain lung cancers and pancreatic cancers. It is most effective in patients whose tumors have specific EGFR mutations.

Berat Molekul

393,4380 g/mol

LogP

3,30

TPSA

74,70 Ų

Lipinski RO5

Lulus

Area Terapeutik

Kelas Obat

Mekanisme Kerja

Reversible inhibitor of EGFR (HER1) tyrosine kinase, blocking autophosphorylation.

Pharmacokinetics (PK)

Half-Life 36 hours

Pharmacodynamics (PD)

Mekanisme

Reversible inhibitor of EGFR (HER1) tyrosine kinase, blocking autophosphorylation.

Struktur 2D

SVG PNG

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SMILES

C#Cc1cccc(Nc2ncnc3cc(OCCOC)c(OCCOC)cc23)c1

InChI

InChI=1S/C22H23N3O4/c1-4-16-6-5-7-17(12-16)25-22-18-13-20(28-10-8-26-2)21(29-11-9-27-3)14-19(18)23-15-24-22/h1,5-7,12-15H,8-11H2,2-3H3,(H,23,24,25)

Molecular Formula

C22H23N3O4

HBD / HBA

1 / 7

Ikatan yang Dapat Dirotasi

11

Atom Berat

29

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

This oral targeted therapy blocks the EGFR protein that drives the growth of cancer cells in certain lung cancers and pancreatic cancers. It is most effective in patients whose tumors have specific EGFR mutations.

Reversible inhibitor of EGFR (HER1) tyrosine kinase, blocking autophosphorylation.

Key pharmacokinetic parameters for Erlotinib: Half-life: 36 hours.

Yes, Erlotinib is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.

Related Drugs

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References & Data Sources

  • ChEMBL — European Bioinformatics Institute (EBI). CHEMBL553. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 176870. Chemical information database.

Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.

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.