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'''Trideca-7,9,11-trienoic acid''', or '''(7E,9E,11E)-trideca-7,9,11-trienoic acid''', is an ]. It is present in '']''.<ref name="three">{{cite journal |last1=Shri |first1=Richa |last2=Bhutani |first2=K.K. |last3=Sharma |first3=Anupam |year=2010 |title=A new anxiolytic fatty acid from Aethusa cynapium |journal=Fitoterapia |volume=81 |issue=5 |pages=337–340 |doi=10.1016/j.fitote.2010.05.003}}</ref><ref name="four">{{Cite web |title=(7E,9E,11E)-trideca-7,9,11-trienoic acid |publisher=National Library of Medicine |work=PubChem |url=https://pubchem.ncbi.nlm.nih.gov/compound/(7E-9E-11E)-trideca-7-9-11-trienoic-acid}} 3.1.2025.</ref><ref name="five">{{Cite patent |title=Composition for ink vehicles and protective coatings |publication-number=EP0503897A1 |inventor=Gerald Sugarman, Michael W. O'Neill |assignee=Topez Co|url=https://patents.google.com/patent/EP0503897A1}} 16.9.1992.</ref> '''Trideca-7,9,11-trienoic acid''', or '''(7E,9E,11E)-trideca-7,9,11-trienoic acid''', is an ]. It is present in '']''.<ref name="three">{{cite journal |last1=Shri |first1=Richa |last2=Bhutani |first2=K.K. |last3=Sharma |first3=Anupam |year=2010 |title=A new anxiolytic fatty acid from Aethusa cynapium |journal=Fitoterapia |volume=81 |issue=5 |pages=337–340 |doi=10.1016/j.fitote.2010.05.003}}</ref><ref name="four">{{Cite web |title=(7E,9E,11E)-trideca-7,9,11-trienoic acid |publisher=National Library of Medicine |work=PubChem |url=https://pubchem.ncbi.nlm.nih.gov/compound/88499374}} 3.1.2025.</ref><ref name="five">{{Cite patent |title=Composition for ink vehicles and protective coatings |publication-number=EP0503897A1 |inventor=Gerald Sugarman, Michael W. O'Neill |assignee=Topez Co|url=https://patents.google.com/patent/EP0503897A1}} 16.9.1992.</ref>


== Pharmacology == == Pharmacology ==

Revision as of 03:22, 3 January 2025

Trideca-7,9,11-trienoic acid
Names
IUPAC name (7E,9E,11E)-trideca-7,9,11-trienoic acid
Identifiers
3D model (JSmol)
ChemSpider
PubChem CID
InChI
  • InChI=1S/C13H20O2/c1-2-3-4-5-6-7-8-9-10-11-12-13(14)15/h2-7H,8-12H2,1H3,(H,14,15)/b3-2+,5-4+,7-6+¨Key: CMKVWQNTXKWDNT-ICDJNDDTSA-N
SMILES
  • C/C=C/C=C/C=C/CCCCCC(=O)O
Properties
Chemical formula C13H20O2
Molar mass 208.301 g·mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Infobox references
Chemical compound

Trideca-7,9,11-trienoic acid, or (7E,9E,11E)-trideca-7,9,11-trienoic acid, is an polyunsaturated fatty acid. It is present in Aethusa cynapium.

Pharmacology

Trideca-7,9,11-trienoic acid has been shown to have an antianxiety effect in Mus musculus, Rattus norvegicus, and Homo sapiens. It reduces hypolocomotion caused by anxiety, which was psychopharmacologically induced with mCPP, in Mus musculus and Rattus norvegicus. A 2 mg/Kg dose of diazepam has a very similar effect to 20 mg/Kg of trideca-7,9,11-trienoic acid.

Extraction from A. cynapium

Trideca-7,9,11-trienoic acid can be extracted from dried aerial parts of A. cynapium with methanol, followed by chloroform, followed by column chromatography with DCM and methanol (40:60), followed by flash chromatography with DCM and methanol (92.5:7.5), followed by preparative TLC.

References

  1. ^ Shri, Richa; Bhutani, K.K.; Sharma, Anupam (2010). "A new anxiolytic fatty acid from Aethusa cynapium". Fitoterapia. 81 (5): 337–340. doi:10.1016/j.fitote.2010.05.003.
  2. "(7E,9E,11E)-trideca-7,9,11-trienoic acid". PubChem. National Library of Medicine. 3.1.2025.
  3. EP0503897A1, Gerald Sugarman, Michael W. O'Neill, "Composition for ink vehicles and protective coatings", assigned to Topez Co  16.9.1992.
  4. Bilkei-Gorzo A, Gyertyar I, Szabados T (1996). "mCPP-induced anxiety—a potential new method for screening anxiolytic activity". Neurobiology. 4: 253–5.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  5. Bilkei-Gorzo A, Gyertyar I, Levay G (1998). "mCPP-induced anxiety in the light–dark box in rats—a new method for screening anxiolytic activity". Psychopharmacology. 136: 291–8.{{cite journal}}: CS1 maint: multiple names: authors list (link)
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