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{{distinguish|cephalin}} {{distinguish|cephalin}}
{{Chembox {{Chembox
| verifiedrevid = 708748834 | verifiedrevid = 708897244
| ImageFile = Cephaeline.svg | ImageFile = Cephaeline.svg
| IUPACName = (1''R'')-1-<nowiki>isoquinolin-2-yl]methyl]-7-methoxy-1,2,3,4-tetrahydroisoquinolin-6-ol | IUPACName = 7′,10,11-Trimethoxyemetan-6′-ol
| SystematicName = (1''R'')-1-{isoquinolin-2-yl]methyl}-7-methoxy-1,2,3,4-tetrahydroisoquinolin-6-ol
| OtherNames = Cepheline; Desmethylemetine; Dihydropsychotrine | OtherNames = Cepheline; Desmethylemetine; Dihydropsychotrine
|Section1={{Chembox Identifiers |Section1={{Chembox Identifiers
| CASNo = 483-17-0 | CASNo = 483-17-0
| CASNo_Ref = {{cascite|correct|CAS}} | CASNo_Ref = {{cascite|correct|CAS}}
⚫ | PubChem = 442195
| ChEMBL = 255708 | ChEMBL = 255708
| ChEMBL_Ref = {{ebicite|correct|EBI}} | ChEMBL_Ref = {{ebicite|correct|EBI}}
⚫ | PubChem = 442195
| KEGG_Ref = {{keggcite|correct|kegg}}
| KEGG = C09390
| UNII = QA971541A1 | UNII = QA971541A1
| UNII_Ref = {{fdacite|correct|FDA}} | UNII_Ref = {{fdacite|correct|FDA}}
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}} }}


'''Cephaeline''' is an ] that is found in '']'' and other plant species including '']''.<ref>{{cite news|url=http://www.accessmylibrary.com/article-1G1-119570434/micropropagaci195179n-de-la-planta.html|title=Micropropagacion de la planta medicinal psychotria acuminata|last=Lara, Alfonso; Valverde, Roberto; Gomez, Luis; Hidalgo, Nancy| date=July 1, 2003 |work=Agronomía Costarricense| accessdate=26 December 2009}}</ref> Cephaeline induces vomiting by stimulating the stomach lining and is found in commercial products such as ].<ref>{{cite news|url=http://www.accessmylibrary.com/article-1G1-72449957/pharma-japan-approval-4.html|title=Pharma Japan: Approval of 4 drugs including Seroquel recommended: CPAC panel.|date=November 14, 2000 |work=Chemical Business Newsbase |accessdate=26 December 2009}}</ref> Chemically, it is closely related to ]. '''Cephaeline''' is an ] that is found in '']'' and other plant species including '']''.<ref>{{cite news|url=http://www.accessmylibrary.com/article-1G1-119570434/micropropagaci195179n-de-la-planta.html|title=Micropropagacion de la planta medicinal psychotria acuminata|author1=Lara, Alfonso |author2=Valverde, Roberto |author3=Gomez, Luis |author4=Hidalgo, Nancy | date=July 1, 2003 |work=Agronomía Costarricense| accessdate=26 December 2009}}</ref> Cephaeline induces vomiting by stimulating the stomach lining and is found in commercial products such as ].<ref>{{cite news|url=http://www.accessmylibrary.com/article-1G1-72449957/pharma-japan-approval-4.html|title=Pharma Japan: Approval of 4 drugs including Seroquel recommended: CPAC panel.|date=November 14, 2000 |work=Chemical Business Newsbase |accessdate=26 December 2009}}</ref> Chemically, it is closely related to ].


==Poison treatment== ==Poison treatment==
Cephaeline in the form of syrup of ipecac was once commonly recommended as an emergency treatment for accidental poisoning, but its use has been phased out due to its ineffectiveness.<ref>{{cite journal |journal=Pediatrics |volume=112 |issue=5 |date=November 2003 |pages=1182–1185 |title=Policy statement: Poison treatment in the home |url=http://aappolicy.aappublications.org/cgi/content/full/pediatrics;112/5/1182 |doi=10.1542/peds.112.5.1182 |pmid=14595067| accessdate=31 December 2009}}</ref> Cephaeline in the form of syrup of ipecac was once commonly recommended as an emergency treatment for accidental poisoning, but its use has been phased out due to its ineffectiveness.<ref>{{cite journal |journal=Pediatrics |volume=112 |issue=5 |date=November 2003 |pages=1182–1185 |title=Policy statement: Poison treatment in the home |doi=10.1542/peds.112.5.1182 |pmid=14595067 |doi-access=free |last1=American Academy Of Pediatrics Committee On Injury |first1=Violence }}</ref>


== References == == References ==
{{Reflist}} {{Reflist}}

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