CHEBI:15393 - (+)-borneol

ChEBI IDCHEBI:15393
ChEBI Name(+)-borneol
Stars
Secondary ChEBI IDsCHEBI:14, CHEBI:10756, CHEBI:18440
Last Modified19 April 2018
SubmitterMarcus Ennis
DownloadsMolfile
FormulaC10H18O
Net Charge0
Average Mass154.253
Monoisotopic Mass154.13577
SMILESCC1(C)[C@@H]2CC[C@@]1(C)[C@@H](O)C2
InChIInChI=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
InChIKeyDTGKSKDOIYIVQL-WEDXCCLWSA-N
Roles Classification
Biological Roles:
volatile oil component  Any plant metabolite that is found naturally as a component of a volatile oil.
metabolite  Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
ChEBI Ontology
Outgoing Relation(s)
(+)-borneol (CHEBI:15393) is a borneol (CHEBI:28093)
(+)-borneol (CHEBI:15393) is enantiomer of (−)-borneol (CHEBI:15394)
Incoming Relation(s)
(+)-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 
(1R,2S,4R)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol
Synonyms  Source
(1R,2S,4R)-borneolChemIDplus
(1R-endo)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-olChemIDplus
(1R,2S,4R)-(+)-BorneolKEGG COMPOUND
BorneocamphorKEGG COMPOUND
(+)-BorneolKEGG COMPOUND
d-BorneolKEGG COMPOUND
UniProt Name  Source
(1R,2S,4R)-borneolUniProt
Manual XrefsDatabases
C00011023KNApSAcK
C01765KEGG COMPOUND
C01765KEGG COMPOUND
Registry NumbersSources
Beilstein:2038056Beilstein
CAS:464-43-7KEGG COMPOUND
CAS:464-43-7ChemIDplus