CHEBI:15405 - (−)-endo-fenchol

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name (−)-endo-fenchol
ChEBI ID CHEBI:15405
ChEBI ASCII Name (-)-endo-fenchol
Definition A fenchane monoterpenoid that is bicyclo[2.2.1]heptane substituted by methyl groups at positions 1, 3 and 3 and a hydroxy group at position 2 (the 1S,2S,4R stereoisomer).
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:131, CHEBI:10768, CHEBI:18482
Supplier Information
Download Molfile XML SDF
Formula C10H18O
Net Charge 0
Average Mass 154.24932
Monoisotopic Mass 154.13577
InChI InChI=1S/C10H18O/c1-9(2)7-4-5-10(3,6-7)8(9)11/h7-8,11H,4-6H2,1-3H3/t7-,8-,10+/m1/s1
InChIKey IAIHUHQCLTYTSF-MRTMQBJTSA-N
SMILES CC1(C)[C@@H]2CC[C@@](C)(C2)[C@@H]1O
Roles Classification
Biological Role(s): plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
volatile oil component
Any plant metabolite that is found naturally as a component of a volatile oil.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing (−)-endo-fenchol (CHEBI:15405) has role plant metabolite (CHEBI:76924)
(−)-endo-fenchol (CHEBI:15405) has role volatile oil component (CHEBI:27311)
(−)-endo-fenchol (CHEBI:15405) is a carbobicyclic compound (CHEBI:36785)
(−)-endo-fenchol (CHEBI:15405) is a fenchane monoterpenoid (CHEBI:36739)
IUPAC Name
(1S,2S,4R)-1,3,3-trimethylbicyclo[2.2.1]heptan-2-ol
Synonyms Sources
(-)-endo-Fenchol KEGG COMPOUND
(-)-endo-Fenchol KEGG COMPOUND
(1S,2-endo)-1,3,3-trimethylnorbornan-2-ol JCBN
(1S,2S,4R)-endo-fenchol UniProt
1,3,3-trimethyl-2-norbornanol ChEBI
2-Fenchanol KEGG COMPOUND
α-fenchol NIST Chemistry WebBook
α-fenchyl alcohol NIST Chemistry WebBook
endo-α-fenchol NIST Chemistry WebBook
endo-fenchol NIST Chemistry WebBook
Fenchyl alcohol KEGG COMPOUND
Manual Xrefs Databases
C00035801 KNApSAcK
C02344 KEGG COMPOUND
CPD-685 MetaCyc
HMDB0034932 HMDB
LMPR0102120005 LIPID MAPS
View more database links
Registry Numbers Types Sources
1632-73-1 CAS Registry Number KEGG COMPOUND
2038083 Reaxys Registry Number Reaxys
2038083 Beilstein Registry Number ChemIDplus
2094057 Gmelin Registry Number Gmelin
3648192 Beilstein Registry Number Beilstein
512-13-0 CAS Registry Number ChemIDplus
512-13-0 CAS Registry Number NIST Chemistry WebBook
Citations Waiting for Citations Types Sources
20334144 PubMed citation Europe PMC
22455514 PubMed citation Europe PMC
Last Modified
04 August 2014