Butalbital
A barbiturate with sedative properties, typically found in combination products used to treat tension headaches and migraines, often combined with acetaminophen and caffeine. It works by relaxing muscle contraction and producing central nervous system sedation. It carries a risk of medication-overuse headache and physical dependence with frequent use.
分子量
224.2600 g/mol
LogP
1.70
TPSA
75.30 Ų
リピンスキーの五則
適合
治療領域
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
C=CCC1(CC(C)C)C(=O)NC(=O)NC1=O
InChI
InChI=1S/C11H16N2O3/c1-4-5-11(6-7(2)3)8(14)12-10(16)13-9(11)15/h4,7H,1,5-6H2,2-3H3,(H2,12,13,14,15,16)
Molecular Formula
C11H16N2O3
HBD / HBA
2 / 3
回転可能結合数
4
重原子数
16
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
A barbiturate with sedative properties, typically found in combination products used to treat tension headaches and migraines, often combined with acetaminophen and caffeine. It works by relaxing muscle contraction and producing central nervous system sedation. It carries a risk of medication-overuse headache and physical dependence with frequent use.
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, Butalbital 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). CHEMBL454. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 2481. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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