| Weight | 625.593 g/mol |
|---|---|
| Formula | C34H38Cl2N2O5 |
| Hydrogen Acceptors | 6 |
| Hydrogen Donors | 4 |
| Aromatic Rings | 4 |
| Rotatable Bonds | 0 |
Apomorphine hydrochloride (314-19-2, 41372-20-7)
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- Sigma-Aldrich - Apomorphine hydrochloride42.30 - 846.00 USD
- Fisher Scientific - Search for Apomorphine hydrochloride
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- Apomorphine Hydrochloride-Induced Improvement in Huntington's Chorea: Stimulation of Dopamine Receptor (JAMA Neurology, 1978)
- An open-label, randomized, flexible-dose, crossover study to assess the comparative efficacy and safety of sildenafil citrate and apomorphine hydrochloride in men with erectile dysfunction. (BJUI, 2004)
- Influence of apomorphine hydrochloride, dibutyrylapomorphine and Lysenyl on plasma prolactin concentrations in the rat (Journal of Pharmacy and Pharmacology, 1975)
- The crystal and molecular structure of apomorphine hydrochloride hydrate (Acta Crystallographica Section B Structural Crystallography and Crystal Chemistry, 1973)
- CLINICAL EXPERIENCE WITH APOMORPHINE HYDROCHLORIDE: THE FIRST 107 PATIENTS (The Journal of Urology, 2003)
- Combination therapy for erectile dysfunction: a randomized, double blind, unblinded active-controlled, cross-over study of the pharmacodynamics and safety of combined oral formulations of apomorphine hydrochloride, phentolamine mesylate and papaverine hydrochloride in men with moderate to severe erectile dysfunction. (International Journal of Impotence Research, 2002)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCN1CCC2=CC=CC3=C2C1CC4=C3C(=C(C=C4)O)O.CN1CCC2=CC=CC3=C2C1CC4=C3C(=C(C=C4)O)O.O.Cl.Cl
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InChIKeyCXWQXGNFZLHLHQ-UHFFFAOYSA-N
- Pubchem - Apomorphine hydrochloride
- Wikipedia - apomorphine hydrochloride
Apomorphine (brand names Apokyn, Ixense, Spontane, Uprima) is a type of aporphine having activity as a non-selective dopamine agonist which activates both D2-like and, to a much lesser extent, D1-like receptors. It also acts as an antagonist of 5-HT2 and -adrenergic receptors with high affinity. The compound is historically a morphine decomposition product by boiling with concentrated acid, hence the -morphine suffix.
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