Spectroscopic investigations and molecular docking analysis of ML115: A potential molecular probe of the signal transducer and activator of transcription

被引:5
|
作者
Wu, Chengjun [1 ]
Xie, Weibin [1 ]
Li, Linwei [1 ]
Li, Wei [2 ]
Wang, Jian [1 ]
Sun, Tiemin [1 ]
机构
[1] Shenyang Pharmaceut Univ, Minist Educ, Key Lab Struct Based Drug Design & Discovery, Shenyang 110016, Liaoning, Peoples R China
[2] Shenyang Univ Chem Technol, Dept Pharmaceut Engn, Shenyang 110042, Liaoning, Peoples R China
关键词
Isoxazoles carboxamide; X-ray diffraction; IR; DFT; Vibrational assignment; EXPERIMENTAL FT-IR; AB-INITIO HF; VIBRATIONAL SPECTROSCOPY; DFT; RAMAN; DERIVATIVES; INHIBITORS; SPECTRA; NMR; UV;
D O I
10.1016/j.molstruc.2018.08.035
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
Herein, we described the investigation of ML115 as molecular probe of the signal transducer and activator of transcription (STAT3), through organic synthesis, X-ray diffraction and theoretical calculation. Firstly, ML115 was prepared and the single crystal was obtained by slow evaporation method. Single crystal X-ray diffraction study revealed that ML115 possesses monoclinic crystal system having P 21/n space group. Then the conformations were optimized and vibrational spectrum were predicted through density functional theory (DFT), and compared with the crystal structure and experimental results. The vibrational modes were interpreted in terms of potential energy distribution, and molecular electrostatic potentials analysis was carried out to predict the reactive sites of ML115 for electrophilic and nucleophilic attack. Accordingly, the stabilization of the molecular structure was revealed by the frontier orbitals analysis. Furthermore, ML115 was docked into STAT3 pocket to elucidate the mechanism of the agonistic activity. The work would be helpful for understanding the feature of ML115 as molecular probe of STAT3, and thus provide hint for discover more STAT3 probes. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:638 / 647
页数:10
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