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InChI=1S/CH4O/c1-2/h2H,1H3
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ChEBI
> Main
CHEBI:15393 - (+)-borneol
Main
ChEBI Ontology
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ChEBI Name
(+)-borneol
ChEBI ID
CHEBI:15393
Stars
This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs
CHEBI:14, CHEBI:10756, CHEBI:18440
Supplier Information
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Formula
C10H18O
Net Charge
0
Average Mass
154.24932
Monoisotopic Mass
154.13577
InChI
InChI=1S/C10H18O/c1-9(2)7-4-5-10(9,3)8(11)6-7/h7-8,11H,4-6H2,1-3H3/t7-,8+,10+/m1/s1
InChIKey
DTGKSKDOIYIVQL-WEDXCCLWSA-N
SMILES
CC1(C)[C@@H]2CC[C@@]1(C)[C@@H](O)C2
Roles Classification
Biological Role
(s):
metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
(via
borneol
)
volatile oil component
Any plant metabolite that is found naturally as a component of a volatile oil.
(via
borneol
)
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
(+)-borneol (
CHEBI:15393
)
is a
borneol (
CHEBI:28093
)
(+)-borneol (
CHEBI:15393
)
is enantiomer of
(−)-borneol (
CHEBI:15394
)
Incoming
(+)-bornyl acetate (
CHEBI:3151
)
has functional parent
(+)-borneol (
CHEBI:15393
)
(+)-bornyl diphosphate (
CHEBI:15395
)
has functional parent
(+)-borneol (
CHEBI:15393
)
(−)-borneol (
CHEBI:15394
)
is enantiomer of
(+)-borneol (
CHEBI:15393
)
IUPAC Name
(1
R
,2
S
,4
R
)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol
Synonyms
Sources
(+)-Borneol
KEGG COMPOUND
(1R,2S,4R)-(+)-Borneol
KEGG COMPOUND
(1
R
,2
S
,4
R
)-borneol
UniProt
(1
R
,2
S
,4
R
)-borneol
ChemIDplus
(1
R
-
endo
)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol
ChemIDplus
Borneocamphor
KEGG COMPOUND
d-Borneol
KEGG COMPOUND
d
-borneol
ChemIDplus
D
-borneol
ChemIDplus
endo-2-Bornanol
KEGG COMPOUND
Sumatra camphor
KEGG COMPOUND
Manual Xrefs
Databases
C00011023
KNApSAcK
C01765
KEGG COMPOUND
View more database links
Registry Numbers
Types
Sources
2038056
Beilstein Registry Number
Beilstein
464-43-7
CAS Registry Number
KEGG COMPOUND
464-43-7
CAS Registry Number
ChemIDplus
Last Modified
19 April 2018