Cephaeline: Difference between revisions
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{{distinguish|cephalin}} |
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| verifiedrevid = |
| verifiedrevid = 708897244 |
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| ImageFile = Cephaeline.svg |
| ImageFile = Cephaeline.svg |
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| IUPACName = (1''R'')-1- |
| IUPACName = 7′,10,11-Trimethoxyemetan-6′-ol |
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| SystematicName = (1''R'')-1-{[(2''S'',3''R'',11b''S'')-3-Ethyl-9,10-dimethoxy-1,3,4,6,7,11b-hexahydro-2''H''-pyrido[2,1-''a'']isoquinolin-2-yl]methyl}-7-methoxy-1,2,3,4-tetrahydroisoquinolin-6-ol |
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| OtherNames = Cepheline; Desmethylemetine; Dihydropsychotrine |
| OtherNames = Cepheline; Desmethylemetine; Dihydropsychotrine |
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|Section1={{Chembox Identifiers |
|Section1={{Chembox Identifiers |
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| CASNo = 483-17-0 |
| CASNo = 483-17-0 |
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| CASNo_Ref = {{cascite|correct|CAS}} |
| CASNo_Ref = {{cascite|correct|CAS}} |
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| ChEMBL = 255708 |
| ChEMBL = 255708 |
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| ChEMBL_Ref = {{ebicite|correct|EBI}} |
| ChEMBL_Ref = {{ebicite|correct|EBI}} |
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| KEGG_Ref = {{keggcite|correct|kegg}} |
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| KEGG = C09390 |
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| UNII = QA971541A1 |
| UNII = QA971541A1 |
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| UNII_Ref = {{fdacite|correct|FDA}} |
| UNII_Ref = {{fdacite|correct|FDA}} |
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'''Cephaeline''' is an [[alkaloid]] that is found in ''[[Cephaelis ipecacuanha]]'' and other plant species including ''[[cephaelis|Psychotria acuminata]]''.<ref>{{cite news|url=http://www.accessmylibrary.com/article-1G1-119570434/micropropagaci195179n-de-la-planta.html|title=Micropropagacion de la planta medicinal psychotria acuminata| |
'''Cephaeline''' is an [[alkaloid]] that is found in ''[[Cephaelis ipecacuanha]]'' and other plant species including ''[[cephaelis|Psychotria acuminata]]''.<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 [[syrup of ipecac]].<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 [[emetine]]. |
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==Poison treatment== |
==Poison treatment== |
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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 |
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> |
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== References == |
== References == |
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{{Reflist}} |
{{Reflist}} |
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[[Category: |
[[Category:Isoquinoline alkaloids]] |
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[[Category:Phenols]] |
[[Category:Phenols]] |
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[[Category: |
[[Category:Norsalsolinol ethers]] |
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[[Category:Tetrahydroisoquinolines]] |
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[[Category:Pyridoisoquinolines]] |
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[[Category:Emetics]] |
[[Category:Emetics]] |
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[[Category:Drugs with no legal status]] |