CHEBI:74299 - geranyllinalool

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ChEBI Name geranyllinalool
ChEBI ID CHEBI:74299
Definition A diterpenoid that is linalool in which one of the terminal methyl hydrogens is substituted by a geranyl group (the 6E,10E-geoisomer)
Stars This entity has been manually annotated by the ChEBI Team.
Submitter Anonymous
Supplier Information
Download Molfile XML SDF
Formula C20H34O
Net Charge 0
Average Mass 290.48340
Monoisotopic Mass 290.26097
InChI InChI=1S/C20H34O/c1-7-20(6,21)16-10-15-19(5)14-9-13-18(4)12-8-11-17(2)3/h7,11,13,15,21H,1,8-10,12,14,16H2,2-6H3/b18-13+,19-15+
InChIKey IQDXAJNQKSIPGB-HQSZAHFGSA-N
SMILES CC(C)=CCC\C(C)=C\CC\C(C)=C\CCC(C)(O)C=C
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.
EC 2.3.1.50 (serine C-palmitoyltransferase) inhibitor
An EC 2.3.1.* (acyltransferase transferring other than amino-acyl group) inhibitor that interferes with the action of serine palmitoyltransferase (EC 2.3.1.50).
Application(s): fragrance
A substance, extract, or preparation for diffusing or imparting an agreeable or attractive smell.
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ChEBI Ontology
Outgoing geranyllinalool (CHEBI:74299) has role EC 2.3.1.50 (serine C-palmitoyltransferase) inhibitor (CHEBI:59647)
geranyllinalool (CHEBI:74299) has role fragrance (CHEBI:48318)
geranyllinalool (CHEBI:74299) has role metabolite (CHEBI:25212)
geranyllinalool (CHEBI:74299) is a diterpenoid (CHEBI:23849)
geranyllinalool (CHEBI:74299) is a tertiary alcohol (CHEBI:26878)
Incoming lyciumoside II (CHEBI:133834) has functional parent geranyllinalool (CHEBI:74299)
IUPAC Name
(6E,10E)-3,7,11,15-tetramethylhexadeca-1,6,10,14-tetraen-3-ol
Synonyms Sources
(6E,10E)-geranyllinalool UniProt
(E,E)-3,7,11,15-tetramethylhexadeca-1,6,10,14-tetraen-3-ol NIST Chemistry WebBook
(E,E)-geranyllinalool MetaCyc
3,7,11,15-Tetramethyl-1,6,10,14-hexadecatetraen-3-ol ChemIDplus
Geranyl linalool ChemIDplus
Manual Xrefs Databases
CN101070270 Patent
CPD-8848 MetaCyc
View more database links
Registry Numbers Types Sources
1113-21-9 CAS Registry Number NIST Chemistry WebBook
1113-21-9 CAS Registry Number ChemIDplus
1912323 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
1556904 PubMed citation Europe PMC
18398052 PubMed citation Europe PMC
18640234 PubMed citation Europe PMC
21334702 PubMed citation Europe PMC
22040000 PubMed citation Europe PMC
22274813 PubMed citation Europe PMC
Last Modified
07 November 2017