fbpx
Wikipedia

Stearidonic acid

Stearidonic acid (SDA: C18H28O2; 18:4, n-3) is an ω-3 fatty acid, sometimes called moroctic acid. It is biosynthesized from alpha-linolenic acid (ALA: C18H30O2; 18:3, n-3) by the enzyme delta-6-desaturase, that removes two hydrogen (H) atoms from a fatty acid, creating a carbon/carbon double bonding, via an oxygen requiring unsaturation. SDA also act as precursor for the rapid synthesis of longer chain fatty acids, called N-acylethanolamine (NAEs), involved in many important biological processes.[1][2] Natural sources of this fatty acid are the seed oils of hemp, blackcurrant, corn gromwell,[3] and Echium plantagineum, and the cyanobacterium Spirulina. SDA can also be synthesized in a lab. A GMO soybean source is approved by the European Food Safety Authority.[4]

Stearidonic acid
Names
Preferred IUPAC name
(6Z,9Z,12Z,15Z)-Octadeca-6,9,12,15-tetraenoic acid
Identifiers
  • 20290-75-9 Y
3D model (JSmol)
  • Interactive image
ChEBI
  • CHEBI:32389 Y
ChEMBL
  • ChEMBL484430 Y
ChemSpider
  • 4471933 Y
ECHA InfoCard 100.127.224
  • 5312508
UNII
  • P4CEK3495O Y
  • DTXSID20920493
  • InChI=1S/C18H28O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18(19)20/h3-4,6-7,9-10,12-13H,2,5,8,11,14-17H2,1H3,(H,19,20)/b4-3-,7-6-,10-9-,13-12- Y
    Key: JIWBIWFOSCKQMA-LTKCOYKYSA-N Y
  • InChI=1/C18H28O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18(19)20/h3-4,6-7,9-10,12-13H,2,5,8,11,14-17H2,1H3,(H,19,20)/b4-3-,7-6-,10-9-,13-12-
    Key: JIWBIWFOSCKQMA-LTKCOYKYBT
  • O=C(O)CCCC\C=C/C\C=C/C\C=C/C\C=C/CC
Properties
C18H28O2
Molar mass 276.420 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YN ?)

See also

References

  1. ^ Galasso, Incoronata; Russo, Roberto; Mapelli, Sergio; Ponzoni, Elena; Brambilla, Ida M.; Battelli, Giovanna; Reggiani, Remo (2016-05-20). "Variability in Seed Traits in a Collection of Cannabis sativa L. Genotypes". Frontiers in Plant Science. 7: 688. doi:10.3389/fpls.2016.00688. ISSN 1664-462X. PMC 4873519. PMID 27242881.
  2. ^ PubChem. "Stearidonic acid". pubchem.ncbi.nlm.nih.gov. Retrieved 2022-11-22.
  3. ^ "Corn Gromwell". NIAB.
  4. ^ "Scientific Opinion on genetically modified soybean MON 87769". European Food Safety Authority. 2014-05-16. Retrieved 2019-02-18.

stearidonic, acid, c18h28o2, fatty, acid, sometimes, called, moroctic, acid, biosynthesized, from, alpha, linolenic, acid, c18h30o2, enzyme, delta, desaturase, that, removes, hydrogen, atoms, from, fatty, acid, creating, carbon, carbon, double, bonding, oxygen. Stearidonic acid SDA C18H28O2 18 4 n 3 is an w 3 fatty acid sometimes called moroctic acid It is biosynthesized from alpha linolenic acid ALA C18H30O2 18 3 n 3 by the enzyme delta 6 desaturase that removes two hydrogen H atoms from a fatty acid creating a carbon carbon double bonding via an oxygen requiring unsaturation SDA also act as precursor for the rapid synthesis of longer chain fatty acids called N acylethanolamine NAEs involved in many important biological processes 1 2 Natural sources of this fatty acid are the seed oils of hemp blackcurrant corn gromwell 3 and Echium plantagineum and the cyanobacterium Spirulina SDA can also be synthesized in a lab A GMO soybean source is approved by the European Food Safety Authority 4 Stearidonic acid NamesPreferred IUPAC name 6Z 9Z 12Z 15Z Octadeca 6 9 12 15 tetraenoic acidIdentifiersCAS Number 20290 75 9 Y3D model JSmol Interactive imageChEBI CHEBI 32389 YChEMBL ChEMBL484430 YChemSpider 4471933 YECHA InfoCard 100 127 224PubChem CID 5312508UNII P4CEK3495O YCompTox Dashboard EPA DTXSID20920493InChI InChI 1S C18H28O2 c1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 h3 4 6 7 9 10 12 13H 2 5 8 11 14 17H2 1H3 H 19 20 b4 3 7 6 10 9 13 12 YKey JIWBIWFOSCKQMA LTKCOYKYSA N YInChI 1 C18H28O2 c1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 h3 4 6 7 9 10 12 13H 2 5 8 11 14 17H2 1H3 H 19 20 b4 3 7 6 10 9 13 12 Key JIWBIWFOSCKQMA LTKCOYKYBTSMILES O C O CCCC C C C C C C C C C C C CCPropertiesChemical formula C 18H 28O 2Molar mass 276 420 g mol 1Except where otherwise noted data are given for materials in their standard state at 25 C 77 F 100 kPa N verify what is Y N Infobox referencesSee also EditList of omega 3 fatty acids Omega 3 fatty acids Essential fatty acidsReferences EditThis article needs additional citations for verification Please help improve this article by adding citations to reliable sources Unsourced material may be challenged and removed Find sources Stearidonic acid news newspapers books scholar JSTOR September 2007 Learn how and when to remove this template message Galasso Incoronata Russo Roberto Mapelli Sergio Ponzoni Elena Brambilla Ida M Battelli Giovanna Reggiani Remo 2016 05 20 Variability in Seed Traits in a Collection of Cannabis sativa L Genotypes Frontiers in Plant Science 7 688 doi 10 3389 fpls 2016 00688 ISSN 1664 462X PMC 4873519 PMID 27242881 PubChem Stearidonic acid pubchem ncbi nlm nih gov Retrieved 2022 11 22 Corn Gromwell NIAB Scientific Opinion on genetically modified soybean MON 87769 European Food Safety Authority 2014 05 16 Retrieved 2019 02 18 This article about an organic compound is a stub You can help Wikipedia by expanding it vte Retrieved from https en wikipedia org w index php title Stearidonic acid amp oldid 1125480975, wikipedia, wiki, book, books, library,

article

, read, download, free, free download, mp3, video, mp4, 3gp, jpg, jpeg, gif, png, picture, music, song, movie, book, game, games.