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Results 1 - 10 of 85 > >>
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EC Number IC50 Value IC50 Value Maximum Inhibitor Commentary Reference
Show all pathways known for 2.7.1.33Display the word mapDisplay the reaction diagram Show all sequences 2.7.1.330.0004 0.0016 pantothenamide, N-substituted IC50 about 0.0004-0.0016 mM 641398
Show all pathways known for 2.7.1.33Display the word mapDisplay the reaction diagram Show all sequences 2.7.1.330.0035 - N-pentylpantothenamide IC50 is 0.0035 mM, has antimicrobial activity against Staphylococcus aureus 662408
Show all pathways known for 2.7.1.33Display the word mapDisplay the reaction diagram Show all sequences 2.7.1.330.0048 - N-heptylpantothenamide IC50 is 0.0048 mM, potent growth inhibitory anti-metabolite 662408
Show all pathways known for 2.7.1.33Display the word mapDisplay the reaction diagram Show all sequences 2.7.1.330.05 0.15 4-(2,4-dihydroxy-3,3-dimethylbutylamido)butyric acid competitive inhibitor, IC50: 0.05-0.15 mM 673027
Show all pathways known for 2.7.1.33Display the word mapDisplay the reaction diagram Show all sequences 2.7.1.330.2 - CoA IC50: 0.2 mM 674852
Show all pathways known for 2.7.1.33Display the word mapDisplay the reaction diagram Show all sequences 2.7.1.330.00006 - acetyl-CoA IC50: 60 nM, competitive inhibitor with respect to ATP 676884
Show all pathways known for 2.7.1.33Display the word mapDisplay the reaction diagram Show all sequences 2.7.1.330.0000625 - acetyl-CoA - 686741
Show all pathways known for 2.7.1.33Display the word mapDisplay the reaction diagram Show all sequences 2.7.1.330.000125 - acetyl-CoA - 686741
Show all pathways known for 2.7.1.33Display the word mapDisplay the reaction diagram Show all sequences 2.7.1.330.0001 - Fusidic acid isoform PanK3, at pH 7.5 and 37°C 722018
Show all pathways known for 2.7.1.33Display the word mapDisplay the reaction diagram Show all sequences 2.7.1.330.0004 - 1,4-phenylene-bis(1,2-ethanediyl)bis-isothiourea dihydrobromide isoform PanK3, at pH 7.5 and 37°C 722018
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