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Results 1 - 10 of 61 > >>
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EC Number Inhibitors Commentary Structure
Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.2521,3,8-Trihydroxynaphthalene competitive to 1,3,6,8-tetrahydroxynaphthalene Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.2521-[(Z)-2-bromo-2-nitroethenyl]-3-fluorobenzene high in vivo activities against Magnaporthe oryzae, EC50 9.5 ppm Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.2521-[(Z)-2-bromo-2-nitroethenyl]-4-ethylbenzene beta-nitrostyrene compound highest inhibitory activity among compounds analyzed Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.2521H-indene-1,3(2H)-dione - Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.2522,3,4,5,6-Pentachlorobenzyl alcohol - Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.2522,3-Dihydro-2,5-dihydroxy-4H-benzopyran-4-one DDBO, an artificial substrate, chemical synthesis method development, overview Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.2522,3-Dihydro-2,5-dihydroxy-4H-benzopyran-4-one activity of the holoenzyme is inhibited by high substrate concentrations. Apigenin prevents the substrate inhibition at high substrate concentrations Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.2523,7-dihydroxyflavone inhibits by 24% Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.2523,7-dihydroxyflavone - Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.2523-hydroxyflavone inhibits by 22% Go to the Ligand Summary Page
Results 1 - 10 of 61 > >>
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