Synthesis of 3-Methoxy-6-[(2, 4, 6-trimethyl-phenylamino)-methyl]-phenol Schiff base characterized by spectral, in-silco and in-vitro studies

被引:0
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作者
Murugan, Suganya [1 ]
Nehru, Jayasudha [1 ]
Arputharaj, David Stephen [2 ]
Paul, Anaglit Catherine [1 ]
Gunasekaran, Prasanth [3 ]
Dege, Necmi [4 ]
cinar, Emine Berrin [4 ]
Balasubramani, Kasthuri [5 ]
Savaridasson, Jose Kavitha [1 ]
Al-Sehemi, Abdullah G. [6 ]
Rajakannan, Venkatachalam [3 ]
Hemamalini, Madhukar [1 ]
机构
[1] Mother Teresa Womens Univ, Dept Chem, Kodaikanal, India
[2] PSG Coll Arts & Sci, Dept Phys, Coimbatore, India
[3] Univ Madras, Ctr Adv Study Crystallog & Biophys, Chennai, India
[4] Ondoku Mayis Univ, Dept Phys, Samsun, Turkey
[5] Govt Arts Coll Autonomous, Dept Chem, Karur, India
[6] King Khalid Univ, Res Ctr Adv Mat Sci, Abha 61413, Saudi Arabia
关键词
Crystal structure; DFT; Molecular docking; Swiss ADME studies; NCI index; Anti -bacterial activity and MTT-assay; Crystal data; Data collection; CRYSTAL-STRUCTURE; PROTEIN; COMPLEXES; DFT;
D O I
10.1016/j.heliyon.2022.e10070
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The structure of the title compound (I) (C17H19NO2)2 the Schiff base, {3-Methoxy-6-[(2,4,6-trimethyl-phenylamino)-methyl]-phenol} was characterized by 1H, 13C NMR, UV-VIS and IR spectroscopic techniques. The crystal structure was determined by X-ray analysis. The compound (I) was crystallized in the Monoclinic space group P21/c, with a = 25.9845 (12), b = 7.3318 (4), c = 16.3543 (8) angstrom, beta = 100.713(degrees) (4), and Z = 8. The intermolecular interactions of the compound (I) was analyzed using Hirshfeld surface and Fingerprint analysis. Based on the crystal-void calculation, the volume of the void and surface area of the Schiff base compound (I) was described. The frontier molecular orbital energy gap reveals charge transfer interactions involving donors and acceptors. The invitro studies on antibacterial property of the title compound shows best MIC value for Staphylococcus aureus and the compound effect on MTT assay on A549 lung cancer cell line. The molecular docking result shows that the compound has good molecular-level interaction with anticancer drug target having good interactions with active site residues. The non-covalent interactions in the protein-ligand complex were well established from NCI analysis.
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页数:14
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