Vemurafenib

CHEMBL1229517 Phase 4 Aprovado Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
489.9 g/mol
LogP
5.0
Phase
4

This targeted therapy is used to treat melanoma that has spread to other parts of the body and carries a specific mutation in the BRAF gene (V600E). It works by blocking the mutated BRAF protein that tells cancer cells to grow uncontrollably. Resistance often develops within months of starting treatment, so it is sometimes combined with MEK inhibitors to prolong effectiveness.

Peso Molecular

489,9000 g/mol

LogP

5,00

TPSA

100,00 Ų

Regra dos 5 de Lipinski

Aprovado

Áreas Terapêuticas

Mecanismo de Ação

Inhibits BRAF kinase, a key component of the RAS/MAPK signaling pathway, blocking constitutive activation that drives cancer cell proliferation in tumors harboring BRAF mutations.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Mecanismo

Inhibits BRAF kinase, a key component of the RAS/MAPK signaling pathway, blocking constitutive activation that drives cancer cell proliferation in tumors harboring BRAF mutations.

Estrutura 2D

SVG PNG

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SMILES

CCCS(=O)(=O)Nc1ccc(F)c(C(=O)c2c[nH]c3ncc(-c4ccc(Cl)cc4)cc23)c1F

InChI

InChI=1S/C23H18ClF2N3O3S/c1-2-9-33(31,32)29-19-8-7-18(25)20(21(19)26)22(30)17-12-28-23-16(17)10-14(11-27-23)13-3-5-15(24)6-4-13/h3-8,10-12,29H,2,9H2,1H3,(H,27,28)

Molecular Formula

C23H18ClF2N3O3S

HBD / HBA

2 / 7

Ligações Rotacionáveis

7

Átomos Pesados

33

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.

Perguntas frequentes

This targeted therapy is used to treat melanoma that has spread to other parts of the body and carries a specific mutation in the BRAF gene (V600E). It works by blocking the mutated BRAF protein that tells cancer cells to grow uncontrollably. Resistance often develops within months of starting treatment, so it is sometimes combined with MEK inhibitors to prolong effectiveness.

Inhibits BRAF kinase, a key component of the RAS/MAPK signaling pathway, blocking constitutive activation that drives cancer cell proliferation in tumors harboring BRAF mutations.

Yes, Vemurafenib 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). CHEMBL1229517. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 42611257. Chemical information database.

Data aggregated from publicly available pharmacological databases. Last updated 2026-03-28.

Aviso Médico

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.