1-(3-Methylthiophene-2-yl)-N-(3,4,5-trimethoxyphenyl)methanimine: Synthesis, Spectroscopic Characterization, Antileishmanial Activity, and DFT and In Silico Studies

被引:0
|
作者
Evecen, M. [1 ]
Celik, F. [2 ]
Guler, H. I. [3 ]
Direkel, S. [4 ]
Unver, Y. [2 ]
机构
[1] Amasya Univ, Fac Arts & Sci, Dept Phys, TR-05100 Amasya, Turkiye
[2] Karadeniz Tech Univ, Fac Sci, Dept Chem, TR-61080 Trabzon, Turkiye
[3] Karadeniz Tech Univ, Fac Sci, Dept Mol Biol & Genet, TR-61080 Trabzon, Turkiye
[4] Giresun Univ, Espiye Vocat Sch, TR-26800 Espiye, Giresun, Turkiye
关键词
thiophene; 3,4,5-trimethoxybenzene; IR and NMR spectroscopy; antileishmanial activity; molecular docking; BIOLOGICAL-ACTIVITY; SCHIFF-BASE; THIOPHENE DERIVATIVES; ANTIOXIDANT; LEISHMANIA; COMPLEXES;
D O I
10.1134/S1070428024090240
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
1-(3-Methylthiophen-2-yl)-N-(3,4,5-trimethoxyphenyl)methanimine (1, MTM) was synthesized from 3-methylthiophene-2-carbaldehyde and 3,4,5-trimethoxyaniline and characterized by FTIR and H-1 and C-13 NMR spectra. The geometric structure of the title compound was optimized, and its electronic (FMO, NLO, MEP, NBO), spectroscopic (NMR, IR, UV), and thermodynamic properties were calculated by quantum chemicial methods. The calculated and experimental geometric parameters were compared with each other. Compound 1 was tested for leishmanicidal activity against Leishmania infantum by the broth microdilution method and was found to be efficient against Leishmania infantum promastigotes in the concentration range studied. Possible interactions responsible for the antileishmanial activity were determined by molecular docking analysis against trypanothione reductase (TRe). The docking results demonstrated high inhibition constant of the title compound and supported its antileishmanial activity.
引用
收藏
页码:1799 / 1809
页数:11
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