The effect of 2‐phenylisatogen on oxidative phosphorylation in rat liver mitochondria

@article{Sweetman1971TheEO,
  title={The effect of 2‐phenylisatogen on oxidative phosphorylation in rat liver mitochondria},
  author={A. J. Sweetman and A. P. Green and M. Hooper},
  journal={FEBS Letters},
  year={1971},
  volume={14}
}
  • A. J. Sweetman, A. P. Green, M. Hooper
  • Published 1971
  • Medicine, Biology
  • FEBS Letters
    • Oligomycin A, N&V’-dicyclohexylcarbodiimide (DCCD) and aurovertin are examples of compounds that have been shown to inhibit ATP synthesis in mitochondria [ 1,2] . These compounds have proved to be useful in the elucidation of the mechanism of reactions associated with electron transport and oxidative phosphorylation such as the ATP-dependent reduction of NAD+ by succinate and the ATP-dependent reduction of NADP+ by NADH [3]. We have examined the effect of the novel heterocyclic compound 2… CONTINUE READING
    View on Wiley
    febs.onlinelibrary.wiley.com
    9 Citations
    Background Citations
    1

    Topics from this paper

    Explore Further: Topics Discussed in This Paper

      9 Citations
      Citation Type

      Citation Type

      2‐Phenylisatogen as an electron acceptor for mitochondrial NADH dehydrogenase
      • 1
      The interaction of 2-phenylisatogen and menadione with rat liver mitochondrial NADH dehydrogenase.
      • 5
      The mechanism of inhibition by 2,2'-pyridylisatogen tosylate of NADPH-linked enzyme activities in microsomes isolated from rat liver.
      2-phenylcarbamoylisatogen, a novel uncoupler of mitochondrial oxidative phosphorylation.
      • 2
      Energy-linked reactions in mitochondria: the effects of some inhibitors and their use in the location of the transhydrogenase enzyme.
      • 6
      ANTAGONISM OF THE INHIBITORY EFFECTS OF ADENOSINE 5′‐TRIPHOSPHATE ON THE ISOLATED TAENIA OF THE GUINEA‐PIG CAECUM: STRUCTURE‐ACTIVITY RELATIONSHIPS WITHIN A SERIES OF ISATOGEN DERIVATIVES
      • 20
      Isatogens and Indolones
      • 8
      Mitochondrial coupling factors.
      • 8
      Discovery and evaluation of inhibitors to the immunosuppressive enzyme indoleamine 2,3-dioxygenase 1 (IDO1): Probing the active site-inhibitor interactions.
      • 13