Vinyl Chloride

CHEMBL2311071 Phase 4 Approuvé Small molecule

Half-Life

—

Bioavailability

—

Protein Binding

—

Molecular Weight

62.5 g/mol

LogP

1.5

Phase

4

Vinyl chloride (chloroethylene) is an industrial chemical and known human carcinogen classified as a Group 1 carcinogen by IARC, primarily associated with hepatic angiosarcoma and other liver cancers upon chronic occupational exposure. It is metabolized to reactive epoxide intermediates that form DNA adducts, causing mutations in oncogenes and tumor suppressor genes. In medical contexts, it is studied as an occupational toxicant and chemical carcinogen model rather than as a therapeutic agent.

Masse moléculaire

62,5000 g/mol

LogP

1,50

TPSA

0,00 Å²

Règle des 5 de Lipinski

Conforme

Aires thérapeutiques

Infectious Disease Age-Related Macular Degeneration Pain Management Chronic Pain

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Structure 2D

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SMILES

C=CCl

InChI

InChI=1S/C2H3Cl/c1-2-3/h2H,1H2

Molecular Formula

C2H3Cl

HBD / HBA

- / -

Liaisons Rotatives

0

Atomes Lourds

3

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

Vinyl chloride (chloroethylene) is an industrial chemical and known human carcinogen classified as a Group 1 carcinogen by IARC, primarily associated with hepatic angiosarcoma and other liver cancers upon chronic occupational exposure. It is metabolized to reactive epoxide intermediates that form DNA adducts, causing mutations in oncogenes and tumor suppressor genes. In medical contexts, it is studied as an occupational toxicant and chemical carcinogen model rather than as a therapeutic agent.

Yes, Vinyl Chloride 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). CHEMBL2311071. Open-access bioactivity database.
PubChem — National Center for Biotechnology Information (NCBI). CID 6338. Chemical information database.

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

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Structure

Données Clés

Formule: C2H3Cl

Liens externes

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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.