CHEBI:15397 - (S)-camphor

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ChEBI Name (S)-camphor
ChEBI ID CHEBI:15397
ChEBI ASCII Name (S)-camphor
Definition The S-enantiomer of camphor.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:85, CHEBI:10774, CHEBI:18479
Supplier Information
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Formula C10H16O
Net Charge 0
Average Mass 152.23344
Monoisotopic Mass 152.12012
InChI InChI=1S/C10H16O/c1-9(2)7-4-5-10(9,3)8(11)6-7/h7H,4-6H2,1-3H3/t7-,10+/m0/s1
InChIKey DSSYKIVIOFKYAU-OIBJUYFYSA-N
SMILES CC1(C)[C@H]2CC[C@]1(C)C(=O)C2
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.
(via camphor )
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ChEBI Ontology
Outgoing (S)-camphor (CHEBI:15397) is a camphor (CHEBI:36773)
(S)-camphor (CHEBI:15397) is enantiomer of (R)-camphor (CHEBI:15396)
Incoming (R)-camphor (CHEBI:15396) is enantiomer of (S)-camphor (CHEBI:15397)
IUPAC Name
(1S,4S)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one
Synonyms Sources
(−)-bornan-2-one ChemIDplus
(−)-camphor NIST Chemistry WebBook
(-)-Camphor KEGG COMPOUND
(1S)-(−)-camphor NIST Chemistry WebBook
(1S,4S)-camphor UniProt
l-camphor ChemIDplus
Manual Xref Database
C00809 KEGG COMPOUND
View more database links
Registry Numbers Types Sources
1907612 Reaxys Registry Number Reaxys
1907612 Beilstein Registry Number Beilstein
4291747 Beilstein Registry Number Beilstein
464-48-2 CAS Registry Number KEGG COMPOUND
464-48-2 CAS Registry Number NIST Chemistry WebBook
464-48-2 CAS Registry Number ChemIDplus
874917 Gmelin Registry Number Gmelin
Last Modified
13 November 2017