CHEBI:36773 - camphor

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ChEBI Name camphor
ChEBI ID CHEBI:36773
Definition A cyclic monoterpene ketone that is bornane bearing an oxo substituent at position 2. A naturally occurring monoterpenoid.
Stars This entity has been manually annotated by the ChEBI Team.
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Formula C10H16O
Net Charge 0
Average Mass 152.23340
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
InChIKey DSSYKIVIOFKYAU-UHFFFAOYSA-N
SMILES CC1(C)C2CCC1(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.
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ChEBI Ontology
Outgoing camphor (CHEBI:36773) has role plant metabolite (CHEBI:76924)
camphor (CHEBI:36773) is a bornane monoterpenoid (CHEBI:22912)
camphor (CHEBI:36773) is a cyclic monoterpene ketone (CHEBI:23446)
Incoming 5-hydroxycamphor (CHEBI:20570) has functional parent camphor (CHEBI:36773)
6-hydroxycamphor (CHEBI:64814) has functional parent camphor (CHEBI:36773)
camphorsulfonic acid (CHEBI:55379) has functional parent camphor (CHEBI:36773)
(R)-camphor (CHEBI:15396) is a camphor (CHEBI:36773)
(S)-camphor (CHEBI:15397) is a camphor (CHEBI:36773)
IUPAC Names
1,7,7-trimethylbicyclo[2.2.1]heptan-2-one
bornan-2-one
Synonyms Sources
2-bornanone NIST Chemistry WebBook
2-camphanone NIST Chemistry WebBook
2-keto-1,7,7-trimethylnorcamphane ChemIDplus
camphor UniProt
Camphor KEGG COMPOUND
camphor ChemIDplus
Formosa camphor NIST Chemistry WebBook
gum camphor ChemIDplus
Japan camphor NIST Chemistry WebBook
Kampfer NIST Chemistry WebBook
laurel camphor NIST Chemistry WebBook
root bark oil ChemIDplus
spirit of camphor ChemIDplus
Manual Xrefs Databases
470 DrugCentral
C00000135 KNApSAcK
C00809 KEGG COMPOUND
C18369 KEGG COMPOUND
Camphor Wikipedia
Camphor MetaCyc
D00098 KEGG DRUG
DB01744 DrugBank
LMPR0102120001 LIPID MAPS
View more database links
Registry Numbers Types Sources
1907611 Beilstein Registry Number ChemIDplus
3196099 Reaxys Registry Number Reaxys
3196099 Beilstein Registry Number ChemIDplus
464-48-2 CAS Registry Number KEGG COMPOUND
6475830 Beilstein Registry Number Beilstein
76-22-2 CAS Registry Number NIST Chemistry WebBook
76-22-2 CAS Registry Number ChemIDplus
83275 Gmelin Registry Number Gmelin
Citations Waiting for Citations Types Sources
17488023 PubMed citation Europe PMC
19384733 PubMed citation Europe PMC
20950270 PubMed citation Europe PMC
21562741 PubMed citation Europe PMC
21620923 PubMed citation Europe PMC
21777420 PubMed citation Europe PMC
21906366 PubMed citation Europe PMC
Last Modified
22 September 2021