Cyclobarbital Calcium
A calcium salt form of cyclobarbital with the same barbiturate sedative properties as the parent compound. It has been used to treat sleep disorders and anxiety.
Moleküler Ağırlık
510,6000 g/mol
TPSA
163,00 Ų
Etki Mekanizması
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 Yapı
Cite this structure
Embed this structure
SMILES
CCC1(C2=CCCCC2)C(=O)[N-]C(=O)NC1=O.CCC1(C2=CCCCC2)C(=O)[N-]C(=O)NC1=O.[Ca+2]
InChI
InChI=1S/2C12H16N2O3.Ca/c2*1-2-12(8-6-4-3-5-7-8)9(15)13-11(17)14-10(12)16;/h2*6H,2-5,7H2,1H3,(H2,13,14,15,16,17);/q;;+2/p-2
Molecular Formula
C24H30CaN4O6
HBD / HBA
2 / 6
Döndürülebilir Bağlar
4
Ağır Atomlar
35
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.
Sıkça Sorulan Sorular
A calcium salt form of cyclobarbital with the same barbiturate sedative properties as the parent compound. It has been used to treat sleep disorders and anxiety.
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 Calcium 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). CHEMBL2106556. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 13293232. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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