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Infections caused by nontuberculous mycobacteria have increased more than 50% in the past two decades and more than doubled in the elderly population. (Mab), one of the most prevalent of these rapidly growing species, is intrinsically resistant to numerous antibiotics. Current standard-of-care treatments are not satisfactory, with high failure rate and notable adverse effects. We report here a potent anti-Mab compound from the flexible molecular framework afforded by conjugated oligoelectrolytes (COEs). A screen of structurally diverse, noncytotoxic COEs identified a lead compound, COE-PNH, which was bactericidal against replicating, nonreplicating persisters and intracellular Mab.COE-PNH had low propensity for resistance development, with a frequency of resistance below 1.25 × 10 and showed no detectable resistance upon serial passaging. Mechanism of action studies were in line with COE-PNH affecting the physical and functional integrity of the bacterial envelope and disrupting the mycomembrane and associated essential bioenergetic pathways. Moreover, COE-PNH was well-tolerated and efficacious in a mouse model of Mab lung infection. This study highlights desirable in vitro and in vivo potency and safety index of this COE structure, which represents a promising anti-mycobacterial to tackle an unmet medical need.
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http://dx.doi.org/10.1126/scitranslmed.adi7558 | DOI Listing |
Microb Pathog
November 2024
Theevanam Additives Nutraceuts Pvt Ltd, IITM Bioincubator, Department of Biotechnology, IIT Madras, Chennai, 600036, India; Saveetha Dental College and Hospitals, SIMATS, Chennai, 600077, India. Electronic address:
Sci Transl Med
February 2024
Department of Chemistry, National University of Singapore, 4 Science Drive 2, 117543 Singapore, Singapore.
Molecules
December 2022
Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Egyptian Russian University, Badr City 11829, Egypt.
We describe the design and synthesis of two isatin-tethered quinolines series (- and -), in connection with our research interest in developing novel isatin-bearing anti-tubercular candidates. In a previous study, a series of small molecules bearing a quinoline-3-carbohydrazone moiety was developed as anti-tubercular agents, and compound disclosed the highest potency with MIC value equal to 6.24 µg/mL.
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February 2023
Leicester School of Pharmacy, De Montfort University, Leicester, UK.
Mol Divers
October 2022
Combi-Chem Bio-Resource Centre, Organic Chemistry Division, CSIR-National Chemical Laboratory, Pune, Maharashtra, 411 008, India.
Herein, we identified a potent lead compound RRA2, within a series of 54 derivatives of 1,2,4-triazolethiols (exhibit good potency as an anti-mycobacterial agents) against intracellular Mycobacterium tuberculosis (Mtb). Compound RRA2 showed significant mycobactericidal activity against active stage Mycobacterium bovis BCG and Mtb with minimum inhibitory concentration (MIC) values of 2.3 and 2.
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