Erlotinib Hydrochloride

CHEMBL1079742 Phase 4 Approuvé Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
429.9 g/mol
LogP
Phase
4

Reversible inhibition of the epidermal growth factor receptor tyrosine kinase is the pharmacology of erlotinib hydrochloride, which prevents receptor autophosphorylation and thereby interrupts downstream proliferative signalling. Tumours carrying activating EGFR mutations depend on that pathway, and it is in such tumours that the agent slows growth. The hydrochloride salt is the form presented in standard oral capsules, chosen for pharmaceutical rather than pharmacological reasons. Reversibility of binding distinguishes this generation of EGFR inhibitors from the covalent agents developed subsequently. The salt has the formula C22H24ClN3O4 and a molecular weight of approximately 429.9 g/mol, and it is approved with development completed through the final phase.

The hydrochloride salt form of erlotinib, this targeted cancer drug blocks the EGFR signaling pathway to slow the growth of EGFR-mutated tumors. The hydrochloride salt formulation is used in standard oral capsules.

Masse moléculaire

429,9000 g/mol

TPSA

74,70 Ų

Aires thérapeutiques

Mécanisme d'action

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

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Mécanisme

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

Structure 2D

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SMILES

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

InChI

InChI=1S/C22H23N3O4.ClH/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);1H

Molecular Formula

C22H24ClN3O4

HBD / HBA

2 / 7

Liaisons Rotatives

11

Atomes Lourds

30

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.

Foire aux questions

The hydrochloride salt form of erlotinib, this targeted cancer drug blocks the EGFR signaling pathway to slow the growth of EGFR-mutated tumors. The hydrochloride salt formulation is used in standard oral capsules.

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

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

{# 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). CHEMBL1079742. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 176871. Chemical information database.

Data aggregated from publicly available pharmacological databases. Last updated 2026-08-20.

Avertissement médical

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.