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> Main
CHEBI:36773 - camphor
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ChEBI Ontology
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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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Wikipedia
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Read full article at Wikipedia
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.
View more via ChEBI Ontology
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
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