CHEBI:15384 - limonene

Main

ChEBI Ontology

Automatic Xrefs

Reactions

Pathways

Models

ChEBI Name limonene ChEBI ID CHEBI:15384 Definition A monoterpene that is cyclohex-1-ene substituted by a methyl group at position 1 and a prop-1-en-2-yl group at position 4 respectively. Stars This entity has been manually annotated by the ChEBI Team. Secondary ChEBI IDs CHEBI:6463, CHEBI:18466, CHEBI:14506 Supplier Information eMolecules:498518 Download Molfile XML SDF Find compounds which contain this structure Find compounds which resemble this structure Take structure to the Advanced Search Formula C10H16 Net Charge 0 Average Mass 136.23404 Monoisotopic Mass 136.12520 InChI InChI=1S/C10H16/c1-8(2)10-6-4-9(3)5-7-10/h4,10H,1,5-7H2,2-3H3 InChIKey XMGQYMWWDOXHJM-UHFFFAOYSA-N SMILES CC(=C)C1CCC(C)=CC1 Metabolite of Species Details Homo sapiens (NCBI:txid9606) See: DOI Roles Classification Biological Role(s): human metabolite Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens). View more via ChEBI Ontology ChEBI Ontology Outgoing limonene (CHEBI:15384) has role human metabolite (CHEBI:77746) limonene (CHEBI:15384) is a p-menthadiene (CHEBI:50073) limonene (CHEBI:15384) is a cycloalkene (CHEBI:33643) Incoming limonene monoterpenoid (CHEBI:25040) has parent hydride limonene (CHEBI:15384) limonene-1,2-diol (CHEBI:17219) has parent hydride limonene (CHEBI:15384) (4R)-limonene (CHEBI:15382) is a limonene (CHEBI:15384) (4S)-limonene (CHEBI:15383) is a limonene (CHEBI:15384) IUPAC Names 1-methyl-4-(prop-1-en-2-yl)cyclohex-1-ene p-mentha-1,8-diene Synonyms Sources (±)-(RS)-limonene IUBMB (+/-)-limonene ChEBI 1,8-p-menthadiene ChemIDplus 1-methyl-4-(1-methylethenyl)cyclohexene ChemIDplus 4-isopropenyl-1-methylcyclohexene NIST Chemistry WebBook Cajeputene KEGG COMPOUND Dipentene KEGG COMPOUND dl-Limonene KEGG COMPOUND Kautschin KEGG COMPOUND limonene UniProt Limonene KEGG COMPOUND Manual Xrefs Databases C00000823 KNApSAcK C00003043 KNApSAcK C06078 KEGG COMPOUND c0626 UM-BBD View more database links Registry Numbers Types Sources 138-86-3 CAS Registry Number ChemIDplus 138-86-3 CAS Registry Number NIST Chemistry WebBook 7705-14-8 CAS Registry Number KEGG COMPOUND 774123 Reaxys Registry Number Reaxys Last Modified 10 May 2022