CHEBI:44247 - (15Z)-tetracosenoic acid

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name (15Z)-tetracosenoic acid
ChEBI ID CHEBI:44247
ChEBI ASCII Name (15Z)-tetracosenoic acid
Definition A tetracosenoic acid having a cis-double bond at position 15.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:44244, CHEBI:7526
Supplier Information
Download Molfile XML SDF
Formulae C24H46O2
C24H46O2
Net Charge 0
Average Mass 366.622
Monoisotopic Mass 366.350
InChI InChI=1S/C24H46O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24(25)26/h9-10H,2-8,11-23H2,1H3,(H,25,26)/b10-9-
InChIKey GWHCXVQVJPWHRF-KTKRTIGZSA-N
SMILES OC(CCCCCCCCCCCCC/C=C\CCCCCCCC)=O
Roles Classification
Chemical Role(s): Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Bronsted base).
(via oxoacid )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing (15Z)-tetracosenoic acid (CHEBI:44247) is a tetracosenoic acid (CHEBI:36032)
(15Z)-tetracosenoic acid (CHEBI:44247) is conjugate acid of (15Z)-tetracosenoate (CHEBI:32392)
Incoming α-Neu5Ac-(2→3)-β-D-Gal-(1→4)-β-D-Glc-(1↔1')-Cer(d18:1/24:1(15Z)) (CHEBI:84989) has functional parent (15Z)-tetracosenoic acid (CHEBI:44247)
β-D-galactosyl-(1→4)-β-D-glucosyl-(1↔1)-N-[(15Z)-tetracosenoyl]sphingosine (CHEBI:84765) has functional parent (15Z)-tetracosenoic acid (CHEBI:44247)
β-D-galactosyl-(1↔1ʼ)-N-[(15Z)-tetracosenoyl]sphinganine (CHEBI:90500) has functional parent (15Z)-tetracosenoic acid (CHEBI:44247)
β-D-galactosyl-N-[(15Z)-tetracosenoyl]sphingosine (CHEBI:84747) has functional parent (15Z)-tetracosenoic acid (CHEBI:44247)
β-D-glucosyl-(1↔1ʼ)-N-[(15Z)-tetracosenoyl]sphinganine (CHEBI:84699) has functional parent (15Z)-tetracosenoic acid (CHEBI:44247)
β-D-glucosyl-N-[(15Z)-tetracosenoyl]sphingosine (CHEBI:84746) has functional parent (15Z)-tetracosenoic acid (CHEBI:44247)
(15Z)-tetracosenoyl-CoA (CHEBI:74142) has functional parent (15Z)-tetracosenoic acid (CHEBI:44247)
1-[(6Z,9Z,12Z)-octadecatrienoyl]-2-[(15Z)-tetracosenoyl]-sn-glycero-3-phosphocholine (CHEBI:86422) has functional parent (15Z)-tetracosenoic acid (CHEBI:44247)
1-hexadecanoyl-2-[(15Z)-tetracosenoyl]-sn-glycero-3-phosphocholine (CHEBI:86197) has functional parent (15Z)-tetracosenoic acid (CHEBI:44247)
1-octadecanoyl-2-[(15Z)-tetracosenoyl]-sn-glycero-3-phosphocholine (CHEBI:86219) has functional parent (15Z)-tetracosenoic acid (CHEBI:44247)
1-tetradecanoyl-2-[(15Z)-tetracosenoyl]-sn-glycero-3-phosphocholine (CHEBI:86175) has functional parent (15Z)-tetracosenoic acid (CHEBI:44247)
2-hydroxynervonic acid (CHEBI:85341) has functional parent (15Z)-tetracosenoic acid (CHEBI:44247)
N-(15Z)-tetracosenoylsphingosine (CHEBI:74450) has functional parent (15Z)-tetracosenoic acid (CHEBI:44247)
N-[(15Z)-tetracosenoyl]-tetradecasphing-4-enine-1-phosphoethanolamine (CHEBI:86970) has functional parent (15Z)-tetracosenoic acid (CHEBI:44247)
N-[(15Z)-tetracosenoyl]sphing-4-enine-1-phosphocholine (CHEBI:74535) has functional parent (15Z)-tetracosenoic acid (CHEBI:44247)
N-[(15Z)-tetracosenoyl]sphinganine (CHEBI:74130) has functional parent (15Z)-tetracosenoic acid (CHEBI:44247)
N-[(15Z)-tetracosenoyl]sphinganine-1-phosphocholine (CHEBI:91146) has functional parent (15Z)-tetracosenoic acid (CHEBI:44247)
N-[(15Z)-tetracosenoyl]sphingosine 1-phosphate (CHEBI:134454) has functional parent (15Z)-tetracosenoic acid (CHEBI:44247)
(15Z)-tetracosenoate (CHEBI:32392) is conjugate base of (15Z)-tetracosenoic acid (CHEBI:44247)
IUPAC Name
(15Z)-tetracos-15-enoic acid
Synonyms Sources
(15Z)-Tetracosenoic acid KEGG COMPOUND
(Z)-15-Tetracosenoic acid KEGG COMPOUND
(Z)-tetracos-15-enoic acid ChEBI
15cis-tetracosenoic acid ChEBI
cis-15-tetracosenoic acid CBN
cis15-tetracosenoic acid ChEBI
Nervonic acid KEGG COMPOUND
Nervonic acid KEGG COMPOUND
Nervonsäure ChEBI
selacholeic acid ChEBI
Database Links Databases
C00001230 KNApSAcK
C08323 KEGG COMPOUND
LMFA01030092 LIPID MAPS
View more database links
Registry Numbers Types Sources
1728551 Beilstein Registry Number Beilstein
1728551 Reaxys Registry Number Reaxys
506-37-6 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
12742544 PubMed citation Europe PMC
16394593 PubMed citation Europe PMC
21147856 PubMed citation Europe PMC
8072429 PubMed citation Europe PMC
9075193 PubMed citation Europe PMC
Last Modified
30 June 2017