Amobarbital Sodium
The sodium salt form of amobarbital, a barbiturate that acts on GABA receptors in the brain to produce sedation and sleep. Like other barbiturates, it carries risks of tolerance, dependence, and overdose.
分子量
248.2500 g/mol
TPSA
81.60 Ų
作用機序
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)
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構造
Cite this structure
Embed this structure
SMILES
CCC1(CCC(C)C)C(=O)N=C([O-])NC1=O.[Na+]
InChI
InChI=1S/C11H18N2O3.Na/c1-4-11(6-5-7(2)3)8(14)12-10(16)13-9(11)15;/h7H,4-6H2,1-3H3,(H2,12,13,14,15,16);/q;+1/p-1
Molecular Formula
C11H17N2NaO3
HBD / HBA
1 / 3
回転可能結合数
4
重原子数
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.
よくある質問
The sodium salt form of amobarbital, a barbiturate that acts on GABA receptors in the brain to produce sedation and sleep. Like other barbiturates, it carries risks of tolerance, dependence, and overdose.
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, Amobarbital Sodium is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.
References & Data Sources
- ChEMBL — European Bioinformatics Institute (EBI). CHEMBL2105941. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 23689390. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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