Chloroform

CHEMBL44618 Phase 4 ได้รับการอนุมัติ Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
119.4 g/mol
LogP
2.3
Phase
4

A halogenated hydrocarbon historically used as a general anesthetic and sedative that produces CNS depression through mechanisms affecting chloride channels and other neuronal targets. Its use in medicine has been entirely abandoned due to its narrow therapeutic index, hepatotoxicity, nephrotoxicity, and potential carcinogenicity. It now has only research and industrial chemical applications.

น้ำหนักโมเลกุล

119.3700 g/mol

LogP

2.30

TPSA

0.00 Ų

Lipinski RO5

ผ่าน

ด้านการรักษา

กลไกการออกฤทธิ์

Selectively blocks angiotensin II type 1 (AT1) receptors, preventing the vasoconstrictive and aldosterone-secreting effects of angiotensin II. This results in vasodilation, reduced sodium retention, and decreased blood pressure.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

กลไก

Selectively blocks angiotensin II type 1 (AT1) receptors, preventing the vasoconstrictive and aldosterone-secreting effects of angiotensin II. This results in vasodilation, reduced sodium retention, and decreased blood pressure.

โครงสร้าง 2 มิติ

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SMILES

ClC(Cl)Cl

InChI

InChI=1S/CHCl3/c2-1(3)4/h1H

Molecular Formula

CHCl3

HBD / HBA

- / -

พันธะที่หมุนได้

0

อะตอมหนัก

4

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.

คำถามที่พบบ่อย

A halogenated hydrocarbon historically used as a general anesthetic and sedative that produces CNS depression through mechanisms affecting chloride channels and other neuronal targets. Its use in medicine has been entirely abandoned due to its narrow therapeutic index, hepatotoxicity, nephrotoxicity, and potential carcinogenicity. It now has only research and industrial chemical applications.

Selectively blocks angiotensin II type 1 (AT1) receptors, preventing the vasoconstrictive and aldosterone-secreting effects of angiotensin II. This results in vasodilation, reduced sodium retention, and decreased blood pressure.

Yes, Chloroform 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). CHEMBL44618. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 6212. Chemical information database.

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

ข้อจำกัดความรับผิดชอบทางการแพทย์

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.