# Homolycorine

> Mediated Wiki article. Canonical URL: https://mediated.wiki/source/Homolycorine
> Markdown URL: https://mediated.wiki/source/Homolycorine.md
> Source: https://en.wikipedia.org/wiki/Homolycorine
> Source revision: 1294524604
> License: Creative Commons Attribution-ShareAlike 4.0 International (https://creativecommons.org/licenses/by-sa/4.0/)

{{chembox
| Verifiedfields = changed
| verifiedrevid =
| ImageFile=Homolycorine.svg
| ImageSize=200px
| IUPACName = 9,10-Dimethoxy-1-methyllycorenan-7-one
| SystematicName = (5a''R'',11b''S'',11c''S'')-9,10-Dimethoxy-1-methyl-2,3,5,5a,11b,11c-hexahydro[2]benzopyrano[3,4-''g'']indol-7(1''H'')-one
| OtherNames = 
|Section1={{Chembox Identifiers
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| ChemSpiderID =  141017 
| InChI =
| InChIKey =
| StdInChI_Ref = {{stdinchicite|correct|chemspider}}
| StdInChI = InChI=1S/C18H21NO4/c1-19-7-6-10-4-5-13-16(17(10)19)11-8-14(21-2)15(22-3)9-12(11)18(20)23-13/h4,8-9,13,16-17H,5-7H2,1-3H3/t13-,16-,17-/m1/s1
| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}}
| StdInChIKey = WXZAKVLYZHWSNF-KBRIMQKVSA-N
| CASNo_Ref = {{cascite|changed|??}}
| CASNo= 477-20-3 
| UNII_Ref = {{fdacite|correct|FDA}}
| UNII = T95J9AUU63
| ChEMBL_Ref = {{ebicite|correct|EBI}}
| ChEMBL = 1221973
| PubChem=160473
| ChEBI_Ref = {{ebicite|correct|EBI}}
| ChEBI =
| SMILES = COc1cc2[C@@H]3[C@@H](CC=C4CCN(C)[C@@H]34)OC(=O)c2cc1OC}}
|Section2={{Chembox Properties
| C=18 | H=21 | N=1 | O=4
| Appearance=
| Density=
| MeltingPt=
| BoilingPt=
| Solubility=
  }}
|Section3={{Chembox Hazards
| MainHazards=
| FlashPt=
| AutoignitionPt =
  }}
}}

'''Homolycorine''' is one of a number of [toxic](/source/toxic) [alkaloid](/source/alkaloid)s found in various [Amaryllidaceae](/source/Amaryllidaceae) species such as daffodils (''[Narcissus](/source/Narcissus_(genus))'').

== Sources ==
* [http://europepmc.org/abstract/MED/24526460 Four new Amaryllidaceae alkaloids from Zephyranthes candida. Shitara N,  Hirasawa Y,  Hasumi S,  Sasaki T,  Matsumoto M,  Wong CP,  Kaneda T,  Asakawa Y,  Morita H  (2014 Jul) Journal of natural medicines, 68(3):610-4]
* [http://scripts.iucr.org/cgi-bin/paper?cf1288 Acta Crystallographica]
* [http://pubs.rsc.org/en/content/articlelanding/1955/JR/jr9550001066#!divAbstract T. Kitagawa, W. I. Taylor, S. Uyeo and H. Yajima. The constitution of homolycorine and lycorenine J. Chem. Soc., 1955, 1066-1068 DOI:  10.1039/JR9550001066]
* {{Cite book|last1=Bastida|first1=Jaume|last2=Lavilla|first2=Rodolfo|last3=Viladomat|first3=Francesc Viladomat|editor1-last=Cordell|editor1-first=G. A.|title=Chemical and biological aspects of "Narcissus" alkaloids|date=2006|volume=63|pages=87–179|doi=10.1016/S1099-4831(06)63003-4|pmid=17133715|series=The Alkaloids: Chemistry and Biology|pmc=7118783|isbn=9780124695634}}

Category:Lactones
Category:Alkaloids
category:Dihydroisocoumarins
Category:Phenol ethers
Category:Nitrogen heterocycles

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Adapted from the Wikipedia article [Homolycorine](https://en.wikipedia.org/wiki/Homolycorine) by Wikipedia contributors ([contributor history](https://en.wikipedia.org/wiki/Homolycorine?action=history)). Available under [Creative Commons Attribution-ShareAlike 4.0 International](https://creativecommons.org/licenses/by-sa/4.0/). Changes may have been made.