CHEBI:61699 - (−)-α-gurjunene

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ChEBI Name (−)-α-gurjunene
ChEBI ASCII Name (-)-alpha-gurjunene
Definition A carbotricyclic compound and sesquiterpene that is 1a,2,3,4,4a,5,6,7b-octahydro-1H-cyclopropa[e]azulene which is substituted by methyl groups at positions 1, 1, 4 and 7 (the 1aR,4R,4aR,7bS- diastereoisomer). It has been isolated from several plant species such as Anaphalis nubigena and Jatropha ribifolia.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C15H24
Net Charge 0
Average Mass 204.35110
Monoisotopic Mass 204.18780
InChI InChI=1S/C15H24/c1-9-6-8-12-14(15(12,3)4)13-10(2)5-7-11(9)13/h9,11-12,14H,5-8H2,1-4H3/t9-,11-,12-,14-/m1/s1
SMILES [H][C@]12CCC(C)=C1[C@@]1([H])[C@@]([H])(CC[C@H]2C)C1(C)C
Metabolite of Species Details
Anaphalis nubigena (NCBI:txid595329) See: PubMed
Roles Classification
Biological Role(s): volatile oil component
Any plant metabolite that is found naturally as a component of a volatile oil.
plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
antibacterial agent
A substance (or active part thereof) that kills or slows the growth of bacteria.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing (−)-α-gurjunene (CHEBI:61699) has role antibacterial agent (CHEBI:33282)
(−)-α-gurjunene (CHEBI:61699) has role plant metabolite (CHEBI:76924)
(−)-α-gurjunene (CHEBI:61699) has role volatile oil component (CHEBI:27311)
(−)-α-gurjunene (CHEBI:61699) is a carbotricyclic compound (CHEBI:38032)
(−)-α-gurjunene (CHEBI:61699) is a sesquiterpene (CHEBI:35189)
(−)-α-gurjunene (CHEBI:61699) is enantiomer of (+)-α-gurjunene (CHEBI:132832)
Incoming 5-hydroxy-α-gurjunene (CHEBI:138167) has functional parent (−)-α-gurjunene (CHEBI:61699)
(+)-α-gurjunene (CHEBI:132832) is enantiomer of (−)-α-gurjunene (CHEBI:61699)
Synonym Source
(−)-α-gurjunene UniProt
Manual Xrefs Databases
CPD-12891 MetaCyc
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Registry Numbers Types Sources
1939514 Reaxys Registry Number Reaxys
489-40-7 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
10190971 PubMed citation Europe PMC
19731610 PubMed citation Europe PMC
23365607 PubMed citation Europe PMC
24371539 PubMed citation Europe PMC
Last Modified
24 October 2017