CHEBI:132900 - (+)-homalomenol A

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ChEBI Name (+)-homalomenol A
ChEBI ID CHEBI:132900
Definition A sesquiterpenoid that is perhydroindane which is substituted by a (2-methylprop-1-en-1-yl) group at position 1, methyl groups at positions 3a and 7, and hydroxy groups at positions 4 and 7 (the 1R,3aR,4R,7S,7aR stereoisomer).
Stars This entity has been manually annotated by the ChEBI Team.
Submitter qingping liu
Supplier Information
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Formula C15H26O2
Net Charge 0
Average Mass 238.366
Monoisotopic Mass 238.19328
InChI InChI=1S/C15H26O2/c1-10(2)9-11-5-7-14(3)12(16)6-8-15(4,17)13(11)14/h9,11-13,16-17H,5-8H2,1-4H3/t11-,12-,13-,14+,15+/m1/s1
InChIKey FKMCEEHVCIIPLE-ZSAUSMIDSA-N
SMILES [C@@]12([C@@H](CC[C@@]([C@@]1([C@H](CC2)C=C(C)C)[H])(O)C)O)C
Metabolite of Species Details
Chimonanthus praecox (NCBI:txid13419) Found in fruit (BTO:0000486). See: Phytochem Lett., 2011, 4(3), 271-274
Chimonanthus praecox (NCBI:txid13419) Found in leaf (BTO:0000713). See: Phytochem Lett., 2011, 4(3), 271-274
Homalomena aromatica (NCBI:txid1804071) Found in root (BTO:0001188). See: PubMed
Homalomena occulta (NCBI:txid714477) Found in aerial part (BTO:0001658). See: PubMed
Roles Classification
Biological Role(s): 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 (+)-homalomenol A (CHEBI:132900) has role plant metabolite (CHEBI:76924)
(+)-homalomenol A (CHEBI:132900) is a carbobicyclic compound (CHEBI:36785)
(+)-homalomenol A (CHEBI:132900) is a diol (CHEBI:23824)
(+)-homalomenol A (CHEBI:132900) is a olefinic compound (CHEBI:78840)
(+)-homalomenol A (CHEBI:132900) is a secondary alcohol (CHEBI:35681)
(+)-homalomenol A (CHEBI:132900) is a sesquiterpenoid (CHEBI:26658)
(+)-homalomenol A (CHEBI:132900) is a tertiary alcohol (CHEBI:26878)
IUPAC Name
(1R,3aR,4R,7S,7aR)-3a,7-dimethyl-1-(2-methylprop-1-en-1-yl)octahydro-1H-indene-4,7-diol
Synonym Source
homalomenol A ChEBI
Registry Numbers Types Sources
145400-03-9 CAS Registry Number ChemIDplus
5810527 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
1368861 PubMed citation Europe PMC
17511005 PubMed citation Europe PMC
18975180 PubMed citation Europe PMC
Last Modified
15 August 2016