CHEBI:132831 - β-maaliene

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ChEBI Name β-maaliene
ChEBI ID CHEBI:132831
ChEBI ASCII Name beta-maaliene
Definition A sesquiterpene that is 1a,2,3,3a,4,5,6,7b-octahydro-1H-cyclopropa[a]naphthalene carrying foru methyl substituents at positions 1, 1, 3a and 7.
Stars This entity has been manually annotated by the ChEBI Team.
Submitter qingping liu
Supplier Information
Download Molfile XML SDF
Formula C15H24
Net Charge 0
Average Mass 204.352
Monoisotopic Mass 204.18780
InChI InChI=1S/C15H24/c1-10-6-5-8-15(4)9-7-11-13(12(10)15)14(11,2)3/h11,13H,5-9H2,1-4H3/t11-,13-,15+/m1/s1
InChIKey UPGLJTCDRBIZKP-KYOSRNDESA-N
SMILES [C@@]12([C@](C1(C)C)(CC[C@]3(C2=C(CCC3)C)C)[H])[H]
Metabolite of Species Details
Cyperus articulatus (NCBI:txid1352543) Found in rhizome (BTO:0001181). See: DOI
Nardostachys chinensis (NCBI:txid179860) Also known as Nardostachys jatamansi and Nardostachys grandiflora See: PubMed
Angelica dahurica (NCBI:txid48101) Found in root (BTO:0001188). See: PubMed
Artemisia monosperma (NCBI:txid72348) Found in leaf (BTO:0000713). See: PubMed
Artemisia monosperma (NCBI:txid72348) Found in stem (BTO:0001300). 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.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing β-maaliene (CHEBI:132831) has role plant metabolite (CHEBI:76924)
β-maaliene (CHEBI:132831) has role volatile oil component (CHEBI:27311)
β-maaliene (CHEBI:132831) is a carbotricyclic compound (CHEBI:38032)
β-maaliene (CHEBI:132831) is a polycyclic olefin (CHEBI:35714)
β-maaliene (CHEBI:132831) is a sesquiterpene (CHEBI:35189)
IUPAC Name
(1aR,3aS,7bS)-1,1,3a,7-tetramethyl-1a,2,3,3a,4,5,6,7b-octahydro-1H-cyclopropa[a]naphthalene
Synonym Source
beta-Maaliene KNApSAcK
Manual Xref Database
C00029818 KNApSAcK
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Registry Numbers Types Sources
2554764 Reaxys Registry Number Reaxys
489-29-2 CAS Registry Number NIST Chemistry WebBook
489-29-2 CAS Registry Number KNApSAcK
Citations Waiting for Citations Types Sources
18404355 PubMed citation Europe PMC
19452246 PubMed citation Europe PMC
21657081 PubMed citation Europe PMC
22978234 PubMed citation Europe PMC
IND43854459 Agricola citation Europe PMC
Last Modified
27 January 2017