Cyclobarbital

CHEMBL268164 Phase 4 معتمد Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
236.3 g/mol
LogP
1.8
Phase
4

A barbiturate sedative used historically to treat insomnia and anxiety. It works by enhancing the effects of a calming brain chemical called GABA, producing sedation.

الوزن الجزيئي

236,2700 g/mol

LogP

1,80

TPSA

75,30 Ų

قاعدة ليبينسكي للخمسة

ناجح

آلية العمل

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)

الآلية

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.

البنية ثنائية الأبعاد

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SMILES

CCC1(C2=CCCCC2)C(=O)NC(=O)NC1=O

InChI

InChI=1S/C12H16N2O3/c1-2-12(8-6-4-3-5-7-8)9(15)13-11(17)14-10(12)16/h6H,2-5,7H2,1H3,(H2,13,14,15,16,17)

Molecular Formula

C12H16N2O3

HBD / HBA

2 / 3

الروابط القابلة للدوران

2

الذرات الثقيلة

17

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.

الأسئلة الشائعة

A barbiturate sedative used historically to treat insomnia and anxiety. It works by enhancing the effects of a calming brain chemical called GABA, producing sedation.

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, Cyclobarbital 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). CHEMBL268164. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 5838. Chemical information database.

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

إخلاء المسؤولية الطبية

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.