Product Name | Apomorphine HCl Hydrate |
Description |
Dopamine Agonist |
Purity | >98% (TLC); NMR (Conforms) |
CAS No. | 41372-20-7 |
Molecular Formula | C17H17NO2 • HCl ½H2O |
Molecular Weight | 312.8 |
Field of Use | Not for use in humans. Not for use in diagnostics or therapeutics. For in vitro research use only. |
Storage Temperature | -20ºC |
Shipping Temperature | Shipped Ambient |
Product Type | Agonist |
Solubility | May be dissolved in water (20 mg/ml) |
Source | Synthetic |
Appearance | Gray Powder |
SMILES | CN1CCC2=C3C1CC4=C(C3=CC=C2)C(=C(C=C4)O)O.Cl |
InChI | InChI=1S/C17H17NO2.ClH/c1-18-8-7-10-3-2-4-12-15(10)13(18)9-11-5-6-14(19)17(20)16(11)12;/h2-6,13,19-20H,7-9H2,1H3;1H/t13-;/m1./s1 |
InChIKey | SKYZYDSNJIOXRL-BTQNPOSSSA-N |
Safety Phrases |
Classification: Danger. Hazard Statements: H301 Precautionary Statements: P301 + P310 + P330 |
Cite This Product | Apomorphine HCl Hydrate (StressMarq Biosciences Inc., Victoria BC CANADA, Catalog # SIH-619) |
Alternative Names | Hemihydrate; R-(-)-6ab-aporphine-10,11-diol, hydrochloride; (R)-5,6,6a,7-Tetrahydro-6-methyl-4H-dibenzo[de,g]quinoline-10,11-diol, hydrochloride |
Research Areas | Neurodegeneration, Neuroscience, Parkinson's Disease |
PubChem ID | 9410 |
Scientific Background | Archetypal dopamine pan-receptor agonist. Displays anti-Parkinsons activity in vivo (1,2). Protects against MPTP-induced neurotoxicity in a mouse model (3). In clinical use for Parkinson’s disease (4,5). |
References |
1. Merck Index 14:746 2.Millan M.J., et al. (2002) J. Pharmacol. Exp. Ther. 303:791. 3. Grunblatt E., et al. (1999) Mov. Disord. 1999 14:612. 4. Auffret M., et al.( 2017) J. Neurol. Sci. 372:279. 5. Jenner P.and R Katzenschlager ( 2016) Parkinsonism. Relat. Disord. 33 Suppl 1:S13. |
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