CHEBI:15394 - (−)-borneol

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name (−)-borneol
ChEBI ID CHEBI:15394
ChEBI ASCII Name (-)-borneol
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:83, CHEBI:18478, CHEBI:10773
Supplier Information
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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+/m0/s1
InChIKey DTGKSKDOIYIVQL-QXFUBDJGSA-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:15394) is a borneol (CHEBI:28093)
(−)-borneol (CHEBI:15394) is enantiomer of (+)-borneol (CHEBI:15393)
Incoming (−)-bornyl diphosphate (CHEBI:64298) has functional parent (−)-borneol (CHEBI:15394)
(+)-borneol (CHEBI:15393) is enantiomer of (−)-borneol (CHEBI:15394)
IUPAC Name
(1S,2R,4S)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol
Synonyms Sources
(-)-Borneol KEGG COMPOUND
(1S,2R,4S)-(−)-borneol NIST Chemistry WebBook
(1S,2R,4S)-(-)-Borneol KEGG COMPOUND
(1S,2R,4S)-borneol UniProt
(1S-endo)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol NIST Chemistry WebBook
L-Borneol KEGG COMPOUND
l-borneol ChemIDplus
L-borneol NIST Chemistry WebBook
Linderol KEGG COMPOUND
Database Links Databases
C00011024 KNApSAcK
C01766 KEGG COMPOUND
View more database links
Registry Numbers Types Sources
2038053 Beilstein Registry Number Beilstein
3587558 Beilstein Registry Number Beilstein
464-45-9 CAS Registry Number KEGG COMPOUND
464-45-9 CAS Registry Number NIST Chemistry WebBook
464-45-9 CAS Registry Number ChemIDplus
Last Modified
23 October 2015