Aprobarbital

CHEMBL7863 Phase 4 Одобрено Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
210.2 g/mol
LogP
1.1
Phase
4

A barbiturate sedative-hypnotic that enhances the activity of the inhibitory neurotransmitter GABA to produce sedation and sleep. Its use has largely been replaced by safer alternatives such as benzodiazepines.

Молекулярная масса

210,2300 g/mol

LogP

1,10

TPSA

75,30 Ų

Правило пяти Липинского

Соответствует

Механизм действия

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)

Механизм

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.

2D Структура

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SMILES

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

InChI

InChI=1S/C10H14N2O3/c1-4-5-10(6(2)3)7(13)11-9(15)12-8(10)14/h4,6H,1,5H2,2-3H3,(H2,11,12,13,14,15)

Molecular Formula

C10H14N2O3

HBD / HBA

2 / 3

Вращаемые Связи

3

Тяжёлые Атомы

15

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.

Часто задаваемые вопросы

A barbiturate sedative-hypnotic that enhances the activity of the inhibitory neurotransmitter GABA to produce sedation and sleep. Its use has largely been replaced by safer alternatives such as benzodiazepines.

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, Aprobarbital 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). CHEMBL7863. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 6464. Chemical information database.

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

Медицинский отказ от ответственности

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.