Jump to content

8-Oxogeranial

From Wikipedia, the free encyclopedia

This is an old revision of this page, as edited by Citation bot (talk | contribs) at 12:32, 12 December 2019 (Add: pages, pmid. | You can use this bot yourself. Report bugs here.| Activated by User:Nemo bis | via #UCB_webform). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

8-Oxogeranial
Names
IUPAC name
(2E,6E)-2,6-Dimethyl-2,6-octadienedial
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
  • InChI=1S/C10H14O2/c1-9(6-7-11)4-3-5-10(2)8-12/h5-8H,3-4H2,1-2H3/b9-6+,10-5+
    Key: GRHWFPUCRVCMRY-TXFIJWAUSA-N
  • InChI=1/C10H14O2/c1-9(6-7-11)4-3-5-10(2)8-12/h5-8H,3-4H2,1-2H3/b9-6+,10-5+
    Key: GRHWFPUCRVCMRY-TXFIJWAUBP
  • C/C(=C\C=O)/CC/C=C(\C)/C=O
Properties
C10H14O2
Molar mass 166.220 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

8-Oxogeranial, also incorrectly called 10-oxogeranial, is a monoterpene.[1] The terpenoid is produced by 8-hydroxygeraniol dehydrogenase which uses 8-hydroxygeraniol as its substrate. 8-Oxogeranial is itself a substrate for iridoid synthase which synthesizes cis–trans-iridodial and cis–trans-nepetalactol.[2]

References

  1. ^ Dewick (2009) Medicinal Natural Products: A Biosynthetic Approach.
  2. ^ Miettinen, Karel; Dong, Lemeng; Navrot, Nicolas; Schneider, Thomas; Burlat, Vincent; Pollier, Jacob; Woittiez, Lotte; Van Der Krol, Sander; Lugan, Raphaël; Ilc, Tina; Verpoorte, Robert; Oksman-Caldentey, Kirsi-Marja; Martinoia, Enrico; Bouwmeester, Harro; Goossens, Alain; Memelink, Johan; Werck-Reichhart, Danièle (2014). "The seco-iridoid pathway from Catharanthus roseus". Nature Communications. 5: 3606. Bibcode:2014NatCo...5.....M. doi:10.1038/ncomms4606. PMC 3992524. PMID 24710322.