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:
metabolite  Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
volatile oil component  Any plant metabolite that is found naturally as a component of a volatile oil.
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
(+)-BorneolKEGG COMPOUND
d-BorneolKEGG COMPOUND
BorneocamphorKEGG COMPOUND
endo-2-BornanolKEGG COMPOUND
Sumatra camphorKEGG COMPOUND
(1R,2S,4R)-(+)-BorneolKEGG COMPOUND
UniProt Name  Source
(1R,2S,4R)-borneolUniProt
Manual XrefsDatabases
C01765KEGG COMPOUND
C01765KEGG COMPOUND
C00011023KNApSAcK
Registry NumbersSources
Beilstein:2038056Beilstein
CAS:464-43-7KEGG COMPOUND
CAS:464-43-7ChemIDplus