Synthesis and in Silico Studies of a Benzenesulfonyl Curcumin Analogue as a New Anti Dengue Virus Type 2 (DEN2) NS2B/NS3

被引:14
|
作者
Zamri, Adel [1 ]
Teruna, Hilwan Yuda [1 ]
Rahmawati, Eni Nur [1 ]
Frimayanti, Neni [2 ]
Ikhtiarudin, Ihsan [2 ]
机构
[1] Univ Riau, Fac Math & Nat Sci, Dept Chem, Jalan HR Subrantas KM 12-5, Pekanbaru 28293, Indonesia
[2] Sekolah Tinggi Ilmu Farmasi Riau, Dept Pharm, Jalan Kamboja, Pekanbaru 28293, Indonesia
来源
INDONESIAN JOURNAL OF PHARMACY | 2019年 / 30卷 / 02期
关键词
Curcumin; Dengue virus; Molecular docking; Molecular dynamic; FEVER;
D O I
10.14499/indonesianjpharm30iss2pp84
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Curcumin has been reported can interact with multiple molecular targets involved in a large variety of diseases. Accumulated evidence indicated curcumin plays an inhibitory role against infection of numerous viruses. Some studies have been reported that curcumin can interfere the infection processes of dengue virus. In this work, a benzenesulfonyl curcumin, (3E, 5E)-3,5-bis(4-methoxybenzylidene)-1-(phenylsulfonyl) piperidin-4-one (compound 2) has been synthesized by two steps of reactions. The structure of compound 2 has been established based on the interpretation of spectral data include UV, FT-IR, MS/MS, H-1 and C-13 NMR. Then, the in silico studies have been also performed to predict the potency of compound 2 as inhibitor for dengue virus Type 2 (DEN 2) NS2B/NS3 protease. The in silico studies showed that compound 2 has hydrogen bonding with His51 residue, and amazingly that the other catalytic triad such as Asp75 and Ser135 were also showed interactions with the ligand. It is presumably that this compound showed very good activity against DEN2 and can be developed as a new inhibitor for dengue viruses.
引用
收藏
页码:84 / 90
页数:7
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