| Literature DB >> 28092858 |
Jing Wang1, Teng Yang2, Huang Chen3, Yun-Nan Xu1, Li-Fang Yu1, Ting Liu1, Jie Tang4, Zhengfang Yi3, Cai-Guang Yang5, Wei Xue6, Fan Yang7.
Abstract
A series of novel 9, 13-disubstituted berberine derivatives have been synthesized and evaluated for the antibacterial activities against Staphylococcus aureus, including Newman strain and multidrug-resistant strains (NRS-1, NRS-70, NRS-100, NRS-108, and NRS-271). Compound 20 shows the most potent activity against the growth of Newman strain, with a MIC value of 0.78 μg/mL, which is comparable with the positive control vancomycin. In addition, compound 20, 21, and 33 are highly antistaphylococcal active against five strains of multidrug-resistant S. aureus, with MIC values of 0.78-1.56 μg/mL. Of note, theses antibacterial active compounds have no obvious toxicity to the viability of human fibroblast (HAF) cells at the MIC concentration.Entities:
Keywords: Antistaphylococcal activity; Berberine derivatives; Cytotoxicity; Multidrug-resistant
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Year: 2017 PMID: 28092858 DOI: 10.1016/j.ejmech.2017.01.012
Source DB: PubMed Journal: Eur J Med Chem ISSN: 0223-5234 Impact factor: 6.514