Synthesis, crystal structure, computational investigation, molecular docking analysis and anti-lung cancer activity of novel (Z)-3-amino-2-(cyclohexylidenehydrazono)thiazolidin-4-one

被引:2
|
作者
Ghous, Faraz [1 ]
Shukla, Soni [1 ]
Singh, Ramesh [2 ]
Parveen, Shama [3 ]
Banerjee, Monisha [3 ]
Bishnoi, Abha [1 ]
机构
[1] Univ Lucknow, Dept Chem, Lucknow 226007, Uttar Pradesh, India
[2] Indian Inst Technol, Kanpur 208016, Uttar Pradesh, India
[3] Univ Lucknow, Dept Zool, Lucknow 226007, Uttar Pradesh, India
关键词
Thiazolidin-4-one; X-ray diffraction analysis; Hirshfeld surface; ADMET; A549 cell line; HIRSHFELD SURFACE-ANALYSIS; THIAZOLIDINONE DERIVATIVES; ANTIBACTERIAL ACTIVITY; THIAZOLIDINE-2,4-DIONES; ACID;
D O I
10.1016/j.molstruc.2023.135462
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
Ever since the disease of cancer was discovered, man has been mystified by both its mysterious origin and the even more mystifying mechanisms by which it spreads. Although advances in surgery and ra-diotherapy have significantly impacted cancer treatment, the idea of systemic chemotherapy which is targeted specifically at cancer cells and has minimal side effects remains a strategic goal for the future. A novel thiazolidin-4-one analogue was synthesized by the reaction of 1,2,4,5-tetraazaspiro[5.5]undecane-3-thione with chloroacetic acid. The newly synthesized compound was investigated theoretically as well as experimentally by FT-IR, 1H, 13C NMR and UV-Vis spectra and biologically screened in vitro for its anti-lung cancer activity against A549 cancer cell line. The crystal structure of (Z)-3-amino-2-(cyclohexylidenehydrazono)thiazolidin-4-one has been determined by single crystal X-ray diffraction and revealed that it belongs to monoclinic system with cell dimensions: a = 18.9393 (16) A, b = 5.2747 (4) A, c = 10.9518 (9) A, alpha = 90 degrees, beta = 90.214 (3), gamma = 90 degrees and V = 1082.85 (15) A3. Hirshfeld sur-face analysis was performed to study the nature of intermolecular interactions within the crystal struc-ture via 3D and 2D fingerprint surfaces and to demonstrate H-bonding with close contacts in crys-tal via dnorm surface. A descriptive study of (Z)-3-amino-2-(cyclohexylidenehydrazono)thiazolidin-4-one was done by using density functional theory at DFT/B3LYP/6-311 ++ G (d,p) basis set. Results of NLO analysis, ELF, LOL, NCI, AIM, HOMO-LUMO, first hyperpolarizability and molecular electrostatic potential were reported. Theoretical calculation of ADMET properties suggested that the synthesized compounds have a good pharmacokinetic profile. The results of cytotoxic evaluation indicated that (Z)-3-amino-2-(cyclohexylidenehydrazono)thiazolidin-4-one has broad-spectrum cytotoxic activity with IC50 values of 240 mu M against Human lung carcinoma cell line (A549).(c) 2023 Elsevier B.V. All rights reserved.
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页数:16
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