Jump to content

Indolepropionamide

From Wikipedia, the free encyclopedia

This is an old revision of this page, as edited by Citation bot (talk | contribs) at 14:48, 25 August 2016 (Add: bibcode, year, pages, issue, volume, journal, title, pmid, author pars. 1-6. You can use this bot yourself. Report bugs here.). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

Indolepropionamide
Names
IUPAC name
3-(1H-Indol-3-yl)propanamide
Other names
3-Indolepropionamide; Indole-3-propanamide
Identifiers
3D model (JSmol)
  • InChI=1S/C11H12N2O/c12-11(14)6-5-8-7-13-10-4-2-1-3-9(8)10/h1-4,7,13H,5-6H2,(H2,12,14)
    Key: OTVHXWFANORBAK-UHFFFAOYSA-N
  • c1ccc2c(c1)c(c[nH]2)CCC(=O)N
Properties
C11H12N2O
Molar mass 188.230 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Indolepropionamide (IPAM) is a chemical compound with the molecular formula C11H12N2O. In vitro, IPAM reduces reactive oxygen species by inhibiting oxidative phosphorylation in complex I of the electron transport chain.[1]

See also

References

  1. ^ Poeggeler, Burkhard; Sambamurti, Kumar; Siedlak, Sandra L.; Perry, George; Smith, Mark A.; Pappolla, Miguel A. (2010). "A Novel Endogenous Indole Protects Rodent Mitochondria and Extends Rotifer Lifespan". PLoS ONE. 5 (4): e10206. Bibcode:2010PLoSO...510206P. doi:10.1371/journal.pone.0010206. PMID 20421998.{{cite journal}}: CS1 maint: unflagged free DOI (link)