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使用量子计算方法对β-咔啉进行结构活性分析、光谱研究、生物学和化学性质解释。

Structural activity analysis, spectroscopic investigation, biological and chemical properties interpretation on Beta Carboline using quantum computational methods.

作者信息

Hemachandran K, Anbusrinivasan P, Ramalingam S, Aarthi R, Nithya C K

机构信息

Department of Chemistry, A.V.C. College, Mayiladuthurai, Tamilnadu, India.

Department of Physics, A.V.C. College, Mayiladuthurai, Tamilnadu, India.

出版信息

Heliyon. 2019 Nov 20;5(11):e02788. doi: 10.1016/j.heliyon.2019.e02788. eCollection 2019 Nov.

Abstract

In this methodological work, the structural activity analysis have been carried out on β-Carboline to study the anti cancer activity and the way of improving the biological activity. The molecular spectroscopic tools were used to evaluate all the experimental data like spectral results and data were validated by the computational, HyperChem and Osiris tools. The structural, biological and physico-chemical related analyses have been performed to interpret the properties. The GPCR ligand calculated to be 0.11 for generating pharmacokinetic process, Specified drug information for the compound, was congregated from all types of structural activity which was drawn by spectral and HyperChem data. The σ and π interaction band gap (6.18 eV) ensured the drug consistency. The Mulliken charge process distribution was mapped, the charge orientation assignment was checked; the acquired negative charge potential consignment for the cause of antibiotic impact was verified. The molecular orbital interaction study was carried out to identify the origination of degeneracy of interaction causing drug mechanism. Using NMR spectral pattern, the chemical reaction path was recognized and the nodal region dislocation was distinguished on chemical shift. The Electronegativity (χ) and Electrophilicity charge transfer found to be 3.83 and 0.215, confirmed charge complex transfer for activating drug process in the compound. The molecular nonbonding section was thoroughly observed in order to find the occupancy energy, was the key process to initiate drug activity. The bathochromic electronic shift was observed and the existence of CT complex was discussed. The hindering of toxicity was inspected on inevitable chirality of the compound by specifying VCD spectrum.

摘要

在这项方法学研究工作中,对β-咔啉进行了结构活性分析,以研究其抗癌活性及提高生物活性的方法。使用分子光谱工具评估所有实验数据,如光谱结果,并且数据通过计算工具HyperChem和Osiris进行了验证。进行了与结构、生物学和物理化学相关的分析以解释其性质。计算得出产生药代动力学过程的GPCR配体为0.11,从由光谱和HyperChem数据得出的所有类型的结构活性中汇总了该化合物的特定药物信息。σ和π相互作用带隙(6.18 eV)确保了药物的一致性。绘制了Mulliken电荷过程分布,检查了电荷取向分配;验证了因抗生素作用而获得的负电荷电位分配。进行了分子轨道相互作用研究以确定导致药物作用机制的相互作用简并的起源。利用NMR光谱模式识别了化学反应路径,并在化学位移上区分了节点区域的错位。发现电负性(χ)和亲电电荷转移分别为3.83和0.215,证实了化合物中激活药物过程的电荷络合物转移。对分子非键合部分进行了全面观察以找到占据能,这是启动药物活性的关键过程。观察到了红移电子位移并讨论了CT络合物的存在。通过指定VCD光谱检查了化合物不可避免的手性对毒性的阻碍。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc00/6895699/ef60e3abe1e0/gr1.jpg

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