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Design, synthesis and antistaphylococcal activity of marine pyrrole alkaloid derivatives

机译:海洋吡咯生物碱衍生物的设计,合成及抗葡萄球菌活性

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摘要

A novel set of 16 hybrids of bromopyrrole alkaloids with aroyl hydrazone were designed, synthesized and evaluated for antibacterial and antibiofilm activities against methicillin-resistant Staphylococcus aureus (MRSA; ATCC 43866), methicillin-susceptible Staphylococcus aureus (MSSA; ATCC 35556) and Staphylococcus epidermidis (SE, S. epidermidis ATCC 35984). Of the 16 tested hybrids, 14 exhibited equal or superior antibiofilm activity against MSSA and MRSA relative to standard vancomycin. Compound 4m showed highest potency with antibiofilm activity of 0.39 mu g/mL and 0.78 mu g/mL against MSSA and MRSA, respectively. Thus, this compound could act as a potential lead for further development of new antistaphylococcal drugs.
机译:设计,合成和评估了一组新的16种溴吡咯生物碱与芳酰的杂种,以评估其对耐甲氧西林金黄色葡萄球菌(MRSA; ATCC 43866),耐甲氧西林金黄色葡萄球菌(MSSA; ATCC 35556)的抗菌和抗生物膜活性(SE,表皮葡萄球菌ATCC 35984)。在测试的16个杂种中,相对于标准万古霉素,有14个对MSSA和MRSA具有相同或更高的抗生物膜活性。化合物4m显示出最高的效力,其针对MSSA和MRSA的抗生物膜活性分别为0.39μg/ mL和0.78μg/ mL。因此,该化合物可以作为进一步开发新的抗葡萄球菌药物的潜在先导。

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