CHEBI:15383 - (4S)-limonene

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ChEBI Name (4S)-limonene ChEBI ID CHEBI:15383 ChEBI ASCII Name (4S)-limonene Definition An optically active form of limonene having (4S)-configuration. Stars This entity has been manually annotated by the ChEBI Team. Secondary ChEBI IDs CHEBI:10765, CHEBI:10778, CHEBI:97, CHEBI:10766, CHEBI:18468 Supplier Information 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/t10-/m1/s1 InChIKey XMGQYMWWDOXHJM-SNVBAGLBSA-N SMILES [H][C@@]1(CCC(C)=CC1)C(C)=C Roles Classification Biological Role(s): human metabolite Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens). (via limonene ) View more via ChEBI Ontology ChEBI Ontology Outgoing (4S)-limonene (CHEBI:15383) is a limonene (CHEBI:15384) (4S)-limonene (CHEBI:15383) is enantiomer of (4R)-limonene (CHEBI:15382) Incoming (4S)-4-isopropenyl-1-methyl-2-methylene-7-oxabicyclo[4.1.0]heptane (CHEBI:59103) has parent hydride (4S)-limonene (CHEBI:15383) (7R)-7-isopropenyl-4-methyl-1-oxaspiro[2.5]oct-4-ene (CHEBI:59102) has parent hydride (4S)-limonene (CHEBI:15383) (4R)-limonene (CHEBI:15382) is enantiomer of (4S)-limonene (CHEBI:15383) IUPAC Name (4S)-1-methyl-4-(prop-1-en-2-yl)cyclohex-1-ene Synonyms Sources (−)-(S)-limonene IUBMB (-)-(4S)-Limonene KEGG COMPOUND (-)-(S)-Limonene KEGG COMPOUND (-)-Limonene KEGG COMPOUND (4S)-1-methyl-4-isopropenylcyclohex-1-ene IUBMB (4S)-4-isopropenyl-1-methylcyclohexene ChEBI (4S)-limonene UniProt (S)-(−)-p-mentha-1,8-diene NIST Chemistry WebBook (S)-1-methyl-4-(1-methylethenyl)cyclohexene ChemIDplus (S)-p-mentha-1,8-diene ChemIDplus 4αH-p-mentha-1,8-diene IUPAC L-Limonen ChEBI L-limonene NIST Chemistry WebBook Manual Xrefs Databases C00000803 KNApSAcK C00521 KEGG COMPOUND LMPR0102090002 LIPID MAPS View more database links Registry Numbers Types Sources 2323991 Beilstein Registry Number Beilstein 363574 Gmelin Registry Number Gmelin 5989-54-8 CAS Registry Number ChemIDplus 5989-54-8 CAS Registry Number NIST Chemistry WebBook Last Modified 23 October 2015