CHEBI:67479 - lamesticumin F

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name lamesticumin F
ChEBI ID CHEBI:67479
Definition A triterpenoid of the class of onoceranoid-type terpenoids isolated from the twigs of Lansium domesticum.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C30H50O3
Net Charge 0
Average Mass 458.71620
Monoisotopic Mass 458.37600
InChI InChI=1S/C30H50O3/c1-21(11-9-12-22(2)15-18-27(32)29(6,7)33)13-10-14-24-23(3)16-17-25-28(4,5)26(31)19-20-30(24,25)8/h12-13,16,24-25,27,32-33H,9-11,14-15,17-20H2,1-8H3/b21-13+,22-12+/t24-,25-,27+,30+/m0/s1
InChIKey RYDUWPYFQUMUJP-JAKYJIPASA-N
SMILES C\C(CC\C=C(/C)CC[C@@H](O)C(C)(C)O)=C/CC[C@H]1C(C)=CC[C@H]2C(C)(C)C(=O)CC[C@]12C
Metabolite of Species Details
Lansium domesticum (NCBI:txid201017) Found in twig (BTO:0001411). 95% ethanolic extract of air-dried and powdered twigs See: PubMed
Roles Classification
Biological Role(s): metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
antibacterial agent
A substance (or active part thereof) that kills or slows the growth of bacteria.
plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing lamesticumin F (CHEBI:67479) has role antibacterial agent (CHEBI:33282)
lamesticumin F (CHEBI:67479) has role metabolite (CHEBI:25212)
lamesticumin F (CHEBI:67479) has role plant metabolite (CHEBI:76924)
lamesticumin F (CHEBI:67479) is a cyclic terpene ketone (CHEBI:36130)
lamesticumin F (CHEBI:67479) is a diol (CHEBI:23824)
lamesticumin F (CHEBI:67479) is a hexahydronaphthalenes (CHEBI:142348)
lamesticumin F (CHEBI:67479) is a triterpenoid (CHEBI:36615)
IUPAC Name
(4aR,5S,8aR)-5-[(3E,7E,11R)-11,12-dihydroxy-4,8,12-trimethyltrideca-3,7-dien-1-yl]-1,1,4a,6-tetramethyl-3,4,4a,5,8,8a-hexahydronaphthalen-2(1H)-one
Registry Number Type Source
21534276 Reaxys Registry Number Reaxys
Citation Waiting for Citations Type Source
21401117 PubMed citation Europe PMC
Last Modified
23 September 2018