apomorphine

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ap·o·mor·phine

 (ăp′ə-môr′fēn′)
n.
A poisonous alkaloid, C17H17NO2, that is an analog of morphine and is used medicinally to treat Parkinson's disease and to induce vomiting.
American Heritage® Dictionary of the English Language, Fifth Edition. Copyright © 2016 by Houghton Mifflin Harcourt Publishing Company. Published by Houghton Mifflin Harcourt Publishing Company. All rights reserved.

apomorphine

(ˌæpəˈmɔːfiːn; -fɪn) or

apomorphia

n
(Pharmacology) a white crystalline alkaloid, derived from morphine, that is used medicinally as an emetic, as an expectorant, and in Parkinson's disease. Formula: C17H17NO2
Collins English Dictionary – Complete and Unabridged, 12th Edition 2014 © HarperCollins Publishers 1991, 1994, 1998, 2000, 2003, 2006, 2007, 2009, 2011, 2014

ap•o•mor•phine

(ˌæp əˈmɔr fin, -fɪn)

also ap•o•mor•phin

(-fɪn)

n.
an alkaloid, C17H17NO2, derived from morphine and used as a fast-acting emetic.
[1885–90]
Random House Kernerman Webster's College Dictionary, © 2010 K Dictionaries Ltd. Copyright 2005, 1997, 1991 by Random House, Inc. All rights reserved.
ThesaurusAntonymsRelated WordsSynonymsLegend:
Noun1.apomorphine - a morphine derivative that is not as strong as morphine; used as an emetic and in small doses as a sedative
morphia, morphine - an alkaloid narcotic drug extracted from opium; a powerful, habit-forming narcotic used to relieve pain
Based on WordNet 3.0, Farlex clipart collection. © 2003-2012 Princeton University, Farlex Inc.
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References in periodicals archive
Recent reports [2-4] recommend the use of apomorphine, a dopamine receptor agonist, to predict dopaminergic responsiveness.
M2 PHARMA-April 4, 2018-Sunovion Files NDA for Apomorphine Sublingual Film for Treatment of OFF Episodes Associated with Parkinson's Disease
For assessing drug-induced locomotor function, apomorphine (0.25 mg/kgbody weight dissolved in saline) was injected subcutaneously.
He received levodopa-carbidopa-entacapone and then apomorphine. The patient who became 34 years old in 2011 received DBS to STN in September 2011 because his motor complications did not recover despite receiving treatment.
One hour later, apomorphine (2 mg/kg, s.c.) was administered to each rat.
This revelation is not dissimilar to the wake-up call of finding out William Burroughs did not completely give up junk after his apomorphine cure.
Differential neurobehavioral deficits induced by apomorphine and its oxidation product, 8-0 X 0-apomorphine-semiquinone, in rats.
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