| verifiedrevid = 424953216
| ImageFile = Laudanosine.svg
| ImageSize = 220
| ImageName = Skeletal formula
| IUPACName = (1''S'')-1-[(3,4-dimethoxyphenyl)methyl]-6,7-dimethoxy- 2-methyl-3,4-dihydro-1''H''-isoquinoline ▼
| ImageFile1 = Laudanosine molecule spacefill.png
| ImageSize1 = 180
| ImageName1 = Space-filling model
▲| IUPACNamePIN = (1''S'')-1-[(3,4- dimethoxyphenylDimethoxyphenyl)methyl]-6,7-dimethoxy- 2-methyl- 1,2,3,4- dihydro-1''H''-isoquinolinetetrahydroisoquinoline
| OtherNames = ''N''-Methyl-1,2,3,4-tetrahydropapaverine
|Section1={{Chembox Identifiers
| CASNo_Ref = {{cascite|correct|??}}
| CASNo = 2688-77-9
| UNII_Ref = {{fdacite|correct|FDA}}
| UNII = DA7R5WVN48
| PubChem = 73397
| EINECS = 220-253-2
| EINECSCASNO =
| ChemSpiderID_Ref = {{chemspidercite|changed|chemspider}}
| ChemSpiderID = 66114
| StdInChIKey = KGPAYJZAMGEDIQ-KRWDZBQOSA-N }}
|Section2={{Chembox Properties
| C =21 | H=27 | N=1 | O=4
| Appearance =
| Density =
}}
'''Laudanosine''' or '''''N''-methyltetrahydropapaverine''' is a recognized metabolite<ref name=Fodale>{{cite journal |authorvauthors=Fodale V, Santamaria LB |title=Laudanosine, an atracurium and cisatracurium metabolite |journal=Eur J Anaesthesiol |volume=19 |issue=7 |pages=466–73 |date=July 2002 |pmid=12113608 |doi=10.1017/s0265021502000777}}</ref> of [[atracurium]] and [[cisatracurium]]. Laudanosine decreases the seizure threshold, and thus it can induce seizures if present at sufficient threshold concentrations; however such concentrations are unlikely to be produced consequent to chemodegradable metabolism of clinically administered doses of [[cisatracurium]] or [[atracurium]].
[[Image:SlaapbolOpium R0017601pod cut to demonstrate fluid extraction1.JPGjpg|thumb|left|Capsule of ''Papaver somniferum'' showing latex (opium) exuding from incision. Laudanosine occurs naturally in small amounts (0.1%) in opium. ]]
Laudanosine also occurs naturally in minute amounts (0.1%) in [[opium]], from which it was first isolated in 1871.<ref>{{cite book |chapterurlchapter-url=httphttps://books.google.com/books?id=KxTKLlac60wC&pg=PA55&dqq=laudanosine&sigpg=ACfU3U2OZxmvO0Pl8Jnp8KuGXHzMllcnQA#PPA48,M1PA55 |chapter=The Benzylisoquinoline Alkaloids |author=Burger A |title=The Alkaloids: Chemistry and Physiology |origyearorig-year=1954 |year=2005 |volume=4 |editorveditors=Manske RHFRH, Holmes HL (eds.) |pages=48 |location=New York |publisher=Academic Press |isbn=0-12-469504-3}} Retrieved September 18, 2008 through [[Google Book Search]].</ref> Partial [[Dehydration reaction|dehydrogenation]] of laudanosine will lead to [[papaverine]], the alkaloid found in the opium poppy plant (''Papaver somniferum'').
Laudanosine is a [[benzyltetrahydroisoquinoline]] [[alkaloid]]. It has been shown to interact with [[GABA receptor]]s, [[glycine receptor]]s, [[opioid receptor]]s, and [[nicotinic acetylcholine receptor]]s,<ref name=Fodale/><ref>{{cite journal |authorvauthors=Katz Y, Weizman A, Pick CG, Pasternak GW, Liu L, Fonia O, Gavish M |title=Interactions between laudanosine, GABA, and opioid subtype receptors: implication for laudanosine seizure activity |journal= Brain Res |volume=646 |issue=2 |pages=235–241 |date=May 1994 |pmid=8069669 |doi=10.1016/0006-8993(94)90084-1 |s2cid=35031924 }}</ref><ref>{{cite journal |authorvauthors= Exley R, Iturriaga-Vásquez P, Lukas RJ, Sher E, Cassels BK, Bermudez I |title=Evaluation of benzyltetrahydroisoquinolines as ligands for neuronal nicotinic acetylcholine receptors |journal= Br J Pharmacol |volume=146 |issue=1 |pages=15–24 |date=Sep 2005|pmid=15980871 |doi= 10.1038/sj.bjp.0706307 |pmc= 1576253 }}</ref> but not [[benzodiazepine receptor|benzodiazepine]] or [[muscarinic receptor]]s, which are also involved in epilepsy and other types of seizures.<ref>{{cite journal |authorvauthors= Katz Y, Gavish M |title= Laudanosine does not displace receptor-specific ligands from the benzodiazepinergic or muscarinic receptors |journal= Anesthesiol Anesthesiology|volume=70|issue=1 |pages= 109–111 |date=Jan 1989 |pmid= 2536252 |doi= 10.1097/00000542-198901000-00020 }}</ref>
==References==
{{Reflistreflist|230em}}
{{Navboxes
| title = [[Pharmacodynamics]]
{{Cholinergics}}
| titlestyle = background:#ccccff
{{GABAergics}}
| list1 =
{{Glycinergics}}
{{GABA receptor modulators}}
{{Opioidergics}}
{{Glycine receptor modulators}}
{{Nicotinic acetylcholine receptor modulators}}
[[Category:Tetrahydroisoquinolines]]
{{Opioid receptor modulators}}
}}
{{Components of Opium}}
[[Category:Natural opium alkaloids]]
[[Category:PhenolNorsalsolinol ethers]]
[[Category:Convulsants]]
[[Category:GABAA receptor negative allosteric modulators]]
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