Dorzolamide Hydrochloride
A hydrochloride salt form of dorzolamide used as an eye drop to treat glaucoma and elevated eye pressure. Like the base form, it lowers intraocular pressure by reducing aqueous humor production.
Moleküler Ağırlık
360,9000 g/mol
TPSA
151,00 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
CCN[C@H]1C[C@H](C)S(=O)(=O)c2sc(S(N)(=O)=O)cc21.Cl
InChI
InChI=1S/C10H16N2O4S3.ClH/c1-3-12-8-4-6(2)18(13,14)10-7(8)5-9(17-10)19(11,15)16;/h5-6,8,12H,3-4H2,1-2H3,(H2,11,15,16);1H/t6-,8-;/m0./s1
Molecular Formula
C10H17ClN2O4S3
HBD / HBA
3 / 7
Döndürülebilir Bağlar
3
Ağır Atomlar
20
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 hydrochloride salt form of dorzolamide used as an eye drop to treat glaucoma and elevated eye pressure. Like the base form, it lowers intraocular pressure by reducing aqueous humor production.
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, Dorzolamide Hydrochloride 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). CHEMBL1201162. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 6918132. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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