Synthesis and Bioactivity Evaluation of N-Arylsulfonylindole Analogs Bearing a Rhodanine Moiety as Antibacterial Agents.
Synthesis and Bioactivity Evaluation of N-Arylsulfonylindole Analogs Bearing a Rhodanine Moiety as Antibacterial Agents.
复制标题
含绕丹宁结构的N-芳基磺酰吲哚类似物抗菌剂的合成及生物活性评价
DOI:
10.3390/molecules22060970
复制
发表时间:
2017-06-14
期刊:
影响因子:
--
通讯作者:
Deng XQ
中科院分区:
文献类型:
--
作者:
Song MX;Li SH;Peng JY;Guo TT;Xu WH;Xiong SF;Deng XQ
Due to the rapidly growing bacterial resistance to antibiotics and the scarcity of novel agents under development, bacterial infections are still a pressing global problem, making new types of antibacterial agents, which are effective both alone and in combination with traditional antibiotics, urgently needed. In this paper, seven series of N-arylsulfonylindole analogs 5–11 bearing rhodanine moieties were synthesized, characterized, and evaluated for antibacterial activity. According to the in vitro antimicrobial results, half of the synthesized compounds showed potent inhibition against four Gram-positive bacteria, with MIC values in the range of 0.5–8 µg/mL. For multidrug-resistant strains, compounds 6a and 6c were the most potent, with MIC values of 0.5 µg/mL, having comparable activity to gatifloxacin, moxiflocaxin and norfloxacin and being 128-fold more potent than oxacillin (MIC = 64 µg/mL) and 64-fold more active than penicillin (MIC = 32 µg/mL) against Staphylococcus aureus ATCC 43300.
登录
查看更多内容
DOI:
10.3390/molecules21081070
发表时间:
2016-08-16
期刊:
Molecules (Basel, Switzerland)
影响因子:
--
作者:
Vera G;Lagos CF;Almendras S;Hebel D;Flores F;Valle-Corvalán G;Pessoa-Mahana CD;Mella-Raipán J;Montecinos R;Recabarren-Gajardo G
通讯作者:
Recabarren-Gajardo G
影响因子:
5.6
作者:
Tay SB;Yew WS
通讯作者:
Yew WS
影响因子:
6.7
作者:
Jin, Xin;Zheng, Chang-Ji;Piao, Hu-Ri
通讯作者:
Piao, Hu-Ri
影响因子:
6.7
作者:
Song, Ming-Xia;Zheng, Chang-Ji;Piao, Hu-Ri
通讯作者:
Piao, Hu-Ri
影响因子:
5.2
作者:
Livermore, David M.
通讯作者:
Livermore, David M.