Apomorphine Hydrochloride
The hydrochloride salt of apomorphine, used as a fast-acting rescue therapy for off episodes in Parkinson's disease by stimulating dopamine receptors in the brain. Its quick onset makes it particularly valuable for patients experiencing sudden loss of motor control.
الوزن الجزيئي
625,6000 g/mol
TPSA
88,40 Ų
المجالات العلاجية
آلية العمل
Binds to and activates its target receptor, mimicking the action of the endogenous ligand to produce a specific physiological response.
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Binds to and activates its target receptor, mimicking the action of the endogenous ligand to produce a specific physiological response.
البنية ثنائية الأبعاد
Cite this structure
Embed this structure
SMILES
CN1CCc2cccc3c2[C@H]1Cc1ccc(O)c(O)c1-3.CN1CCc2cccc3c2[C@H]1Cc1ccc(O)c(O)c1-3.Cl.Cl.O
InChI
InChI=1S/2C17H17NO2.2ClH.H2O/c2*1-18-8-7-10-3-2-4-12-15(10)13(18)9-11-5-6-14(19)17(20)16(11)12;;;/h2*2-6,13,19-20H,7-9H2,1H3;2*1H;1H2/t2*13-;;;/m11.../s1
Molecular Formula
C34H38Cl2N2O5
HBD / HBA
7 / 7
الروابط القابلة للدوران
0
الذرات الثقيلة
43
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.
الأسئلة الشائعة
The hydrochloride salt of apomorphine, used as a fast-acting rescue therapy for off episodes in Parkinson's disease by stimulating dopamine receptors in the brain. Its quick onset makes it particularly valuable for patients experiencing sudden loss of motor control.
Binds to and activates its target receptor, mimicking the action of the endogenous ligand to produce a specific physiological response.
Yes, Apomorphine 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). CHEMBL3187985. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 107882. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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