(10E,12Z)-Octadecadienoic acid (BioCAD00000020520)

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Metabolite Card

Formula: C18H32O2 (280.2402)
SMILES: CCCCC\C=C/C=C/CCCCCCCCC(O)=O

Synonyms [en]

(10E,12Z)-Octadecadienoic acid; 10E,12Z-Octadecadienoic acid; 10-trans-12-cis-conjugated linoleic acid; (e,Z)-Octadeca-10,12-dienoic acid; 10-trans-12-cis-Linoleic acid; (10E,12Z)-octadeca-10,12-dienoic acid

Reviewed

Last reviewed on 2024-06-28.

Cite this Page

(10E,12Z)-Octadecadienoic acid. 数据之源,洞见之始. SMRUCC genomics institute, a synthetic life researcher from China. https://biocad_registry.innovation.ac.cn/s/(-)-arctiin (retrieved 2026-01-03) (CAD Registry RN: BioCAD00000020520). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).

Note

Conjugated linoleic acid (CLA) is a collective term for a mixture of positional and geometric isomers of linoleic acid (18:2) in which the two double bonds are conjugated. CLA has been suggested to have effects on human health, including effects on body composition, blood lipids, liver metabolism, insulin sensitivity and immune function, with mixed results. Some reported data suggest that the effects of the substance may be isomer dependent and that cis-9,trans-11 and trans-10,cis-12 conjugated linoleic acids have opposing effects, the later (trans-10,cis-12 CLA) having a relative detrimental effect on blood lipids. (PMID 16477173).

Entity Information

DBLinks

Other DBLinks
  • CAS Registry Number: 2420-56-6
  • PubChem: 5282800
  • PubChem: 5351472
  • ChEBI: ChEBI:44526
  • HMDB: HMDB0005048
  • HMDB: HMDB05048
  • LipidMaps: LMFA01030125
  • LipidMaps: LMFA02000307
  • NCBI MeSH: trans-10,cis-12-conjugated linoleic acid
  • DrugBank: DB04746
  • RefMet: RM0202138
  • MoNA: MetaboBASE1003
  • MoNA: MetaboBASE1004
  • MoNA: MetaboBASE1005
  • MoNA: MetaboBASE1006
  • MoNA: MetaboBASE1007
  • Metlin: METLIN_34801
  • Metlin: METLIN_73836

Class / Ontology

Metabolic Network
ID EC Number Name
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Organism Source

Taxonomy Source

Pathway Synthetic

pathway id name
WikiPathways:WP5324 Octadecanoid formation from linoleic acid
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