Lithium Citrate Anhydrous
A anhydrous salt form of lithium with the same therapeutic properties. A mood-stabilizing element used as lithium salts to treat and prevent episodes of mania, depression, and bipolar disorder, and studied for potential neuroprotective effects in Alzheimer's disease.
Moleküler Ağırlık
210,0000 g/mol
TPSA
141,00 Ų
Terapötik Alanlar
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
O=C([O-])CC(O)(CC(=O)[O-])C(=O)[O-].[Li+].[Li+].[Li+]
InChI
InChI=1S/C6H8O7.3Li/c7-3(8)1-6(13,5(11)12)2-4(9)10;;;/h13H,1-2H2,(H,7,8)(H,9,10)(H,11,12);;;/q;3*+1/p-3
Molecular Formula
C6H5Li3O7
HBD / HBA
1 / 7
Döndürülebilir Bağlar
2
Ağır Atomlar
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.
Sıkça Sorulan Sorular
A anhydrous salt form of lithium with the same therapeutic properties. A mood-stabilizing element used as lithium salts to treat and prevent episodes of mania, depression, and bipolar disorder, and studied for potential neuroprotective effects in Alzheimer's disease.
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, Lithium Citrate Anhydrous 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). CHEMBL1201170. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 13520. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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