Synthesis, spectroscopic investigations, DFT studies, molecular docking and antimicrobial potential of certain new indole-isatin molecular hybrids: Experimental and theoretical approaches

被引:40
作者
Almutairi, Maha S. [1 ]
Zakaria, Azza S. [2 ]
Ignasius, P. Primsa [3 ,4 ]
Al-Wabli, Reem I. [1 ]
Joe, Isaac Hubert [3 ]
Attia, Mohamed I. [1 ,5 ]
机构
[1] King Saud Univ, Dept Pharmaceut Chem, Coll Pharm, Riyadh 11451, Saudi Arabia
[2] Alexandria Univ, Dept Microbiol & Immunol, Fac Pharm, Alexandria 21521, Egypt
[3] Mar Ivanios Coll, Dept Phys, Ctr Mol & Biophys Res, Thiruvananthapuram 695015, Kerala, India
[4] Govt Coll, Dept Phys, Thiruvananthapuram 695541, Kerala, India
[5] Natl Res Ctr, Pharmaceut & Drug Ind Res Div, Med & Pharmaceut Chem Dept, El Bohooth St, Giza 12622, Egypt
关键词
5-Methoxyindole; Isatin; FT-IR; FT-Raman; DFT; Antimicrobial; PHARMACOLOGICAL EVALUATION; FT-RAMAN; DERIVATIVES; RECEPTOR; ANALOGS; ACID; IR; UV;
D O I
10.1016/j.molstruc.2017.10.025
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Indole-isatin molecular hybrids 5a-i have been synthesized and characterized by different spectroscopic methods to be evaluated as new antimicrobial agents against a panel of Gram positive bacteria, Gram negative bacteria, and moulds. Compound 5h was selected as a representative example of the prepared compounds 5a-i to perform computational investigations. Its vibrational properties have been studied using FT-IR and FT-Raman with the aid of density functional theory approach. The natural bond orbital analysis as well as HOMO and LUMO molecular orbitals investigations of compound 5h were carried out to explore its possible intermolecular delocalization or hyperconjugation and its possible interactions with the target protein. Molecular docking of compound 5h predicted its binding mode with the fungal target protein. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:333 / 345
页数:13
相关论文
共 56 条
[1]   Spectroscopic (FT-IR, FT-Raman, UV, 1H and 13C NMR) profiling and computational studies on methyl 5-methoxy-1H-indole-2-carboxylate: A potential precursor to biologically active molecules [J].
Almutairi, Maha S. ;
Xavier, S. ;
Sathish, M. ;
Ghabbour, Hazem A. ;
Sebastian, S. ;
Periandy, S. ;
Al-Wabli, Reem I. ;
Attia, Mohamed I. .
JOURNAL OF MOLECULAR STRUCTURE, 2017, 1133 :199-210
[2]  
[Anonymous], 2008, Reference Method for Broth Dilution Antifungal Susceptibility Testing of Yeasts
[3]  
Third Informational Supplement. CLSI document M27-S3, P28
[4]  
[Anonymous], PERF STAND ANT DISK
[5]  
[Anonymous], 2007, Clinical microbiology procedures handbook
[6]  
[Anonymous], 2011, 21 INFORMATIONAL SUP
[7]  
[Anonymous], CLIN MICROBIOLOGY PR
[8]  
[Anonymous], 2015, Approved standard -M07-A10
[9]  
[Anonymous], MED CHEM
[10]  
[Anonymous], 2008, CLSI document M35-A2