1. Antimycobacterial Activity of New 1,4-Benzoxazine-2-One Derivatives and Its 2-(Arylamino)-4-Oxobut-2-Enoate, Ring-Open Analogues
- Author
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Maria Grazia Mamolo, Alessandro De Logu, A Sanna, Marco Bernecich, Daniele Zampieri, ND, Diego Muñoz-Torrero, Zampieri, Daniele, Bernecich, Marco, Mamolo, MARIA GRAZIA, Sanna, Adriana, and De Logu, Alessandro
- Subjects
chemistry.chemical_classification ,biology ,Chemistry ,Stereochemistry ,medicine.drug_class ,lcsh:A ,Mycobacterium tuberculosi ,Menaquinone (MenB) ,Mycobacterium tuberculosis ,Ring (chemistry) ,Antimycobacterial ,biology.organism_classification ,Electron transport chain ,chemistry.chemical_compound ,Enzyme ,n/a ,Biosynthesis ,MIC ,medicine ,lcsh:General Works - Abstract
Menaquinone is one of the essential components of the electron transport chain in many pathogens and consequently enzymes in its biosynthesis pathway are potential drug targets for the development of novel antibacterial agents. Few years ago, Li et al.1 identified several 1,4-benzoxazine-2-one derivatives, targeting MenB (1,4-dihydroxy-2-naphtoyl-CoA synthase), endowed with high antibacterial activity against Mycobacteria tuberculosis H37Rv with MIC values of 0.6 μg/ml. By these assumptions, we designed and synthesized some analogous compounds in order to investigate the SAR and to discover new potent antimycobacterial derivatives. First of all, we tried to check the activity of several benzoxazine-3-one isosters and, in our case, the derivative showed low antimycobacterial activity (32->64 μg/ml) contradicting the bioisosterism principle. Then, we tried to modify the substituents on the original 1,4-benzoxazin-2-one core and we found some interesting data that will be presented. Moreover, we synthesized some 2-(arylamino)-4-oxobut-2-enoate derivatives as analogues of O-Succinyllbenzoate (OSB), a precursor in the menaquinone biosynthetic pathway. Details on antitubercular activity will be presented.
- Published
- 2017