CHEBI:2443 - actinidine

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ChEBI Name actinidine
ChEBI ID CHEBI:2443
Definition A member of the class of cyclopentapyridines that is 6,7-dihydrocyclopenta[c]pyridine bearing two methyl substituents at positions 4 and 7.
Stars This entity has been manually annotated by the ChEBI Team.
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Formula C10H13N
Net Charge 0
Average Mass 147.21696
Monoisotopic Mass 147.10480
InChI InChI=1S/C10H13N/c1-7-3-4-9-8(2)5-11-6-10(7)9/h5-7H,3-4H2,1-2H3/t7-/m0/s1
InChIKey ZHQQRIUYLMXDPP-ZETCQYMHSA-N
SMILES C[C@H]1CCc2c(C)cncc12
Metabolite of Species Details
Valeriana officinalis (NCBI:txid19953) Found in root (BTO:0001188). See: PubMed
Actinidia polygama (NCBI:txid64480) See: PubMed
Roles Classification
Biological Role(s): pheromone
A semiochemical used in olfactory communication between organisms of the same species eliciting a change in sexual or social behaviour.
plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
(via alkaloid )
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ChEBI Ontology
Outgoing actinidine (CHEBI:2443) has role pheromone (CHEBI:26013)
actinidine (CHEBI:2443) has role plant metabolite (CHEBI:76924)
actinidine (CHEBI:2443) is a cyclopentapyridine (CHEBI:37940)
actinidine (CHEBI:2443) is a pyridine alkaloid (CHEBI:26416)
IUPAC Name
(7S)-4,7-dimethyl-6,7-dihydro-5H-cyclopenta[c]pyridine
Synonyms Sources
(S)-(−)-actidine ChEBI
Actinidine KEGG COMPOUND
Manual Xrefs Databases
Actinidine Wikipedia
C00001961 KNApSAcK
C09910 KEGG COMPOUND
HMDB0030346 HMDB
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Registry Numbers Types Sources
524-03-8 CAS Registry Number KEGG COMPOUND
524-03-8 CAS Registry Number ChemIDplus
81308 Reaxys Registry Number Reaxys
81308 Beilstein Registry Number Beilstein
Citations Waiting for Citations Types Sources
24233898 PubMed citation Europe PMC
547813 PubMed citation Europe PMC
6061704 PubMed citation Europe PMC
Last Modified
30 January 2015