Citreoviridin: Difference between revisions
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== Application in [[ | == Application in [[HRFR]] == | ||
::: '''Citreoviridin''' - Cayman Chemical Company: item number 11319. | ::: '''Citreoviridin''' - Cayman Chemical Company: item number 11319. | ||
::: Citreoviridin was tested as an alternative to oligomycin and has been used at 20 µM concentration to inhibit respiration in intact human glioma T98G cells to the same extent as oligomycin ([[Ruas_2016_PLOS_ONE |Ruas 2016 PLOS_ONE]].) In isolated mitochonria from rat liver and ox heart it fully inhibited ADP-stimulated respiration at sub-micromolar concentrations ([http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1183925/pdf/biochemj00490-0062.pdf Linnett 1978 Biochem J]]). | ::: Citreoviridin was tested as an alternative to oligomycin and has been used at 20 µM concentration to inhibit respiration in intact human glioma T98G cells to the same extent as oligomycin ([[Ruas_2016_PLOS_ONE |Ruas 2016 PLOS_ONE]].) In isolated mitochonria from rat liver and ox heart it fully inhibited ADP-stimulated respiration at sub-micromolar concentrations ([http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1183925/pdf/biochemj00490-0062.pdf Linnett 1978 Biochem J]]). | ||
Revision as of 14:30, 29 August 2017
- high-resolution terminology - matching measurements at high-resolution
Citreoviridin
Description
Citreoviridin is an inhibitor of the ATP synthase which, differently from the FO subunit binding inhibitor oligmycin, binds to the F1 subunit of the ATP synthase.
Reference: Linnett 1978 Biochem J
MitoPedia topics: Inhibitor
Application in HRFR
- Citreoviridin - Cayman Chemical Company: item number 11319.
- Citreoviridin was tested as an alternative to oligomycin and has been used at 20 µM concentration to inhibit respiration in intact human glioma T98G cells to the same extent as oligomycin (Ruas 2016 PLOS_ONE.) In isolated mitochonria from rat liver and ox heart it fully inhibited ADP-stimulated respiration at sub-micromolar concentrations (Linnett 1978 Biochem J]).
