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lycorine (CHEBI:6601)

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ChEBI Name lycorine
ChEBI ID CHEBI:6601
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
See structure as:  Image  Applet
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Formula Source
C16H17NO4 ChEBI
Net Charge 0
Average Mass 287.31050
InChI
InChI=1S/C16H17NO4/c18-11-3-8-1-2-17-6-9-4-12-13(21-7-20-12)5-10(9)14(15(8)17)16(11)19/h3-5,11,14-16,18-19H,1-2,6-7H2/t11-,14-,15+,16+/m0/s1
InChIKey
XGVJWXAYKUHDOO-DANNLKNASA-N
SMILES
[H][C@]12[C@H](O)[C@@H](O)C=C3CCN(Cc4cc5OCOc5cc14)[C@@]23[H]
Metabolite of Species Sources
Isolated from Crinum asiaticum var. sinicum (NCBI:223245) found in leaf (BTO:0000713) PubMed
Isolated from Crinum asiaticum var. sinicum (NCBI:223245) found in bulb (BTO:0000159) PubMed
Roles Classification
Chemical Role(s): protein synthesis inhibitor
A compound, usually an anti-bacterial agent or a toxin, which inhibits the synthesis of a protein.
Biological Role(s): protein synthesis inhibitor
A compound, usually an anti-bacterial agent or a toxin, which inhibits the synthesis of a protein.
metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
(via alkaloid )
View more on the ChEBI Ontology
ChEBI Ontology
Outgoing lycorine (CHEBI:6601) has parent hydride galanthan (CHEBI:35646)
lycorine (CHEBI:6601) has role metabolite (CHEBI:25212)
lycorine (CHEBI:6601) has role protein synthesis inhibitor (CHEBI:48001)
lycorine (CHEBI:6601) is a indolizidine alkaloid (CHEBI:38511)
IUPAC Name
9,10-(methylenedioxy)-3,12-didehydrogalanthan-1α,2β-diol
Synonyms Sources
(−)-lycorine ChEBI
Amarylline ChemIDplus
Galanthidine ChemIDplus
Licorine ChemIDplus
Lycorine KEGG COMPOUND
Narcissine ChemIDplus
Database Links Databases
C00001576 KNApSAcK
C08532 KEGG COMPOUND
View more database links
Registry Numbers Types Sources
476-28-8 CAS Registry Number ChemIDplus
93605 Beilstein Registry Number Beilstein
Last Modified
28 juillet 2014

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