Spectroscopic, quantum chemical, molecular docking and in vitro anticancer activity studies on 5-Methoxyindole-3-carboxaldehyde

被引:42
作者
Jeyaseelan, S. Christopher [1 ]
Premkumar, R. [1 ]
Kaviyarasu, K. [2 ,3 ]
Benial, A. Milton Franklin [1 ]
机构
[1] NMSSVN Coll, PG & Res Dept Phys, Madurai 625019, Tamil Nadu, India
[2] Univ South Africa UNISA, Coll Grad Studies, UNESCO UNISA Africa Chair Nanosci Nanotechnol Lab, POB 392, Pretoria, South Africa
[3] Natl Res Fdn, MRD, Nanosci African Network NANOAFNET, iThemba LABS, 1 Old Faure Rd,POB 722, ZA-7129 Somerset West, Western Cape Pr, South Africa
关键词
5-Methoxyindole-3-carboxaldehyde; DFT; Molecular docking; In vitro cytotoxicity; A549 lung cancer cell lines; Anticancer activity; RECEPTOR TYROSINE KINASE; GROWTH-FACTOR RECEPTOR; DENSITY-FUNCTIONAL THEORY; FT-RAMAN; VIBRATIONAL-SPECTRA; ANTITUMOR-ACTIVITY; LUNG-CANCER; AB-INITIO; INDOLE; IR;
D O I
10.1016/j.molstruc.2019.07.042
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
The FT-IR and FT-Raman spectra of 5-Methoxyindole-3-carboxaldehyde (MICA) molecule were recorded. The experimental and theoretical vibrational wavenumbers were assigned and compared. The non-linear optical (NLO) activity of the molecule was confirmed using second harmonic generation test and compared with theoretical result. The natural bond orbital (NBO) analysis was carried out to evaluate the intramolecular stabilization interactions of the molecule, which are responsible for the bio-activity of the molecule. The molecular electrostatic potential surface, frontier molecular orbitals and Fukui function analysis reveal the charge transfer interactions in the molecule. The total density of states (TDOS), partial density of states (PDOS), and overlap population density of states (OPDOS) studies were performed in order to visualize the molecular orbital contributions of the molecule. The molecular docking analysis was carried out to explore the inhibitory nature of the molecule, which indicates that molecule can acts as a novel inhibitor of lung cancer causing VEGF receptor. In addition, the in vitro cytotoxicity of the molecule confirms the anticancer activity against the human pulmonary epithelial lung cancer cell lines (A549). Hence, the present investigations pave the way for the development of lung cancer drugs. (C) 2019 Elsevier B.V. All rights reserved.
引用
收藏
页码:134 / 146
页数:13
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