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1.1.98.3
Development of 3,5-dinitrophenyl-containing 1,2,4-triazoles and their trifluoromethyl analogues as highly efficient antitubercular agents inhibiting decaprenylphosphoryl-beta-D-ribofuranose 2'-oxidase
Mycobacterium tuberculosis
1.1.98.3
Development of 3,5-dinitrophenyl-containing 1,2,4-triazoles and their trifluoromethyl analogues as highly efficient antitubercular agents inhibiting decaprenylphosphoryl-beta-D-ribofuranose 2'-oxidase
Mycobacterium tuberculosis H37Rv
1.1.98.3
Identification and profiling of hydantoins-A novel class of potent antimycobacterial DprE1 inhibitors
Mycobacterium tuberculosis
1.1.98.3
Identification and profiling of hydantoins-A novel class of potent antimycobacterial DprE1 inhibitors
Mycobacterium tuberculosis H37Rv
1.1.98.3
4-aminoquinolone piperidine amides: noncovalent inhibitors of DprE1 with long residence time and potent antimycobacterial activity
Mycobacterium tuberculosis
1.1.98.3
Analogous mechanisms of resistance to benzothiazinones and dinitrobenzamides in Mycobacterium smegmatis
Mycolicibacterium smegmatis
1.1.98.3
Benzothiazinones are suicide inhibitors of mycobacterial decaprenylphosphoryl-beta-D-ribofuranose 2'-oxidase DprE1
Mycolicibacterium smegmatis
1.1.98.3
Benzothiazinones: prodrugs that covalently modify the decaprenylphosphoryl-beta-D-ribose 2-epimerase DprE1 of Mycobacterium tuberculosis
Mycobacterium tuberculosis
1.1.98.3
Benzothiazinones: prodrugs that covalently modify the decaprenylphosphoryl-beta-D-ribose 2-epimerase DprE1 of Mycobacterium tuberculosis
Mycobacterium tuberculosis H37Rv
1.1.98.3
Characterization of DprE1-mediated benzothiazinone resistance in Mycobacterium tuberculosis
Mycobacterium tuberculosis
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