Target Validation Information | |||||
---|---|---|---|---|---|
TTD ID | T72335 | ||||
Target Name | Bacterial Lethal factor (Bact lef) | ||||
Type of Target |
Clinical trial |
||||
Drug Potency against Target | Drug Info | IC50 = 2300 nM | [4] | ||
3-(2,5-dimethyl-1H-pyrrol-1-yl)benzoic acid | Drug Info | IC50 = 15000 nM | [3] | ||
Bisindolylmaleimide-I | Drug Info | IC50 = 1500 nM | [4] | ||
GNF-PF-600 | Drug Info | IC50 = 3000 nM | [2] | ||
MMI270 | Drug Info | IC50 = 12000 nM | [1] | ||
N-(3,4,5-trihydroxyphenethyl)oleamide | Drug Info | Ki = 1700 nM | [5] | ||
N-(3,4-dihydroxybenzyl)oleamide | Drug Info | IC50 = 15000 nM | [6] | ||
N-hydroxy-4-(2-oleamidoethyl)benzamide | Drug Info | Ki = 6000 nM | [5] | ||
N-hydroxy-4-(oleamidomethyl)benzamide | Drug Info | Ki = 6200 nM | [6] | ||
N-oleoyl-dopamine | Drug Info | Ki = 3000 nM | [5] | ||
NSC-622445 | Drug Info | Ki = 4900 nM | [3] | ||
References | |||||
REF 1 | The discovery of a potent and selective lethal factor inhibitor for adjunct therapy of anthrax infection. Bioorg Med Chem Lett. 2006 Feb 15;16(4):964-8. | ||||
REF 2 | Anthrax lethal factor protease inhibitors: synthesis, SAR, and structure-based 3D QSAR studies. J Med Chem. 2006 Jan 12;49(1):27-30. | ||||
REF 3 | Novel small-molecule inhibitors of anthrax lethal factor identified by high-throughput screening. J Med Chem. 2006 Aug 24;49(17):5232-44. | ||||
REF 4 | Amiodarone and bepridil inhibit anthrax toxin entry into host cells. Antimicrob Agents Chemother. 2007 Jul;51(7):2403-11. | ||||
REF 5 | Inhibitors of anthrax lethal factor. Bioorg Med Chem Lett. 2007 Aug 15;17(16):4575-8. | ||||
REF 6 | Inhibitors of anthrax lethal factor based upon N-oleoyldopamine. Bioorg Med Chem Lett. 2008 Apr 1;18(7):2467-70. | ||||
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