CHEBI:15393 - (+)-borneol

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
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
Download Molfile XML SDF
Formula C10H18O
Net Charge 0
Average Mass 154.24932
Monoisotopic Mass 154.136
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 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 diphosphate (CHEBI:15395) has functional parent (+)-borneol (CHEBI:15393)
(−)-borneol (CHEBI:15394) is enantiomer of (+)-borneol (CHEBI:15393)
IUPAC Name
(1R,2S,4R)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol
Synonyms Sources
(+)-Borneol KEGG COMPOUND
(+)-borneol UniProt
(1R,2S,4R)-(+)-Borneol KEGG COMPOUND
(1R,2S,4R)-borneol ChemIDplus
(1R-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
Database Links 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
13 November 2017