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Results 1 - 10 of 66 > >>
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EC Number Inhibitors Commentary Structure
Show all pathways known for 2.8.1.1Display the word mapDisplay the reaction diagram Show all sequences 2.8.1.12,4-dinitrofluorobenzene - Go to the Ligand Summary Page
Show all pathways known for 2.8.1.1Display the word mapDisplay the reaction diagram Show all sequences 2.8.1.12-mercaptoethanol - Go to the Ligand Summary Page
Show all pathways known for 2.8.1.1Display the word mapDisplay the reaction diagram Show all sequences 2.8.1.12-mercaptoethanol at pH 8.0 Go to the Ligand Summary Page
Show all pathways known for 2.8.1.1Display the word mapDisplay the reaction diagram Show all sequences 2.8.1.12-mercaptoethanol weak Go to the Ligand Summary Page
Show all pathways known for 2.8.1.1Display the word mapDisplay the reaction diagram Show all sequences 2.8.1.12-Naphthalene sulfonate - Go to the Ligand Summary Page
Show all pathways known for 2.8.1.1Display the word mapDisplay the reaction diagram Show all sequences 2.8.1.12-oxoglutarate - Go to the Ligand Summary Page
Show all pathways known for 2.8.1.1Display the word mapDisplay the reaction diagram Show all sequences 2.8.1.12-oxoglutarate incubation of mitochondria with 2-oxoglutarate causes a significant decrease in activity Go to the Ligand Summary Page
Show all pathways known for 2.8.1.1Display the word mapDisplay the reaction diagram Show all sequences 2.8.1.15,5'-dithiobis(2-nitrobenzoic acid) - Go to the Ligand Summary Page
Show all pathways known for 2.8.1.1Display the word mapDisplay the reaction diagram Show all sequences 2.8.1.1anions - Go to the Ligand Summary Page
Show all pathways known for 2.8.1.1Display the word mapDisplay the reaction diagram Show all sequences 2.8.1.1anions inhibited by most anions at rather high concentration, the most active inhibitors are aromatic anions, incubation of mitochondria with sulfate and 2-oxoglutarate causes a significant decrease in activity Go to the Ligand Summary Page
Results 1 - 10 of 66 > >>
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