Antimicrobial Activities and In silico Analysis of Methoxy Amino Chalcone Derivatives

被引:11
|
作者
Suwito, Hery [1 ]
Ni'matuzahroh [2 ]
Kristanti, Alfinda Novi [1 ]
Hayati, Salwa [2 ]
Dewi, Selva Rosyta [2 ]
Amalina, Ilma [3 ]
Puspaningsih, Ni Nyoman Tri [1 ,4 ]
机构
[1] Univ Airlangga, Dept Chem, Fac Sci & Technol, Surabaya, Indonesia
[2] Univ Airlangga, Dept Biol, Fac Sci & Technol, Surabaya, Indonesia
[3] Univ Maarif Hasyim Latif, Fac Med Sci, Sidoarjo, Indonesia
[4] Univ Airlangga, Inst Trop Dis, Prote Study Grp, Surabaya, Indonesia
关键词
Methoxy amino chalcones; antimicrobial; dihydropteroate synthase; INHIBITION; DESIGN;
D O I
10.1016/j.proche.2016.01.017
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A series of methoxy-4'-amino chalcone derivatives were tested for their antimicrobial activities against Escherichia coli ATCC 25923, Staphylococcus aureus ATCC 25922 and Candida albicans ATCC 10231. Furthermore, their molecular interactions with dihydropteroate synthase (DHPS) of E. coli and S. aureus were studied with a docking experiment. Compound 4 ((E)-1-(4-aminophenyl)-3-(2,3-dimethoxyphenyl)prop-2-en-1-one) exhibited the strongest activity, in which its activity was equal to sulfamerazine and sulfadiazine used as positive controls. In addition, it showed a good potential to be used as a wide spectrum antimicrobial agent. The in silico experiment showed that the prepared compounds had higher affinity to DHPS of S. aureus than to DHPS of E. coli. The tested compounds showed high similarity interaction with hydroxymethylpterin pyrophosphate (natural substrate of DHPS) in building intermolecular interactions. (C) 2016 The Authors. Published by Elsevier B.V.
引用
收藏
页码:103 / 111
页数:9
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