key: cord-0023738-d1wweiz9
authors: Shreevatsa, Bhargav; Dharmashekara, Chandan; Swamy, Vikas Halasumane; Gowda, Meghana V.; Achar, Raghu Ram; Kameshwar, Vivek Hamse; Thimmulappa, Rajesh Kumar; Syed, Asad; Elgorban, Abdallah M.; Al-Rejaie, Salim S.; Ortega-Castro, Joaquín; Frau, Juan; Flores-Holguín, Norma; Shivamallu, Chandan; Kollur, Shiva Prasad; Glossman-Mitnik, Daniel
title: Virtual Screening for Potential Phytobioactives as Therapeutic Leads to Inhibit NQO1 for Selective Anticancer Therapy
date: 2021-11-14
journal: Molecules
DOI: 10.3390/molecules26226863
sha: 5c4d0639df87f3ddce9d911b3c1b27eabba71fbd
doc_id: 23738
cord_uid: d1wweiz9

NAD(P)H:quinone acceptor oxidoreductase-1 (NQO1) is a ubiquitous flavin adenine dinucleotide-dependent flavoprotein that promotes obligatory two-electron reductions of quinones, quinonimines, nitroaromatics, and azo dyes. NQO1 is a multifunctional antioxidant enzyme whose expression and deletion are linked to reduced and increased oxidative stress susceptibilities. NQO1 acts as both a tumor suppressor and tumor promoter; thus, the inhibition of NQO1 results in less tumor burden. In addition, the high expression of NQO1 is associated with a shorter survival time of cancer patients. Inhibiting NQO1 also enables certain anticancer agents to evade the detoxification process. In this study, a series of phytobioactives were screened based on their chemical classes such as coumarins, flavonoids, and triterpenoids for their action on NQO1. The in silico evaluations were conducted using PyRx virtual screening tools, where the flavone compound, Orientin showed a better binding affinity score of −8.18 when compared with standard inhibitor Dicumarol with favorable ADME properties. An MD simulation study found that the Orientin binding to NQO1 away from the substrate-binding site induces a potential conformational change in the substrate-binding site, thereby inhibiting substrate accessibility towards the FAD-binding domain. Furthermore, with this computational approach we are offering a scope for validation of the new therapeutic components for their in vitro and in vivo efficacy against NQO1.

NQO1 is one of the two main quinone reductases in the mammalian system. The paralog of cytosolic protein NQO1 is NQO2. NQO1 was isolated in the late 1950s, identified in rat liver, and named DT-diaphorase (DTD) by Lars Ernster. It is highly inducible in rat liver by azo dyes and polycyclic aromatic hydrocarbons regulated by the Keap1/Nrf2/ARE pathway and plays various roles in cellular stress response, including oxidative stress [1] . Under stress conditions, the NQO1 levels can increase rapidly, presumably as a cellular protective system [2] . NQO1 is a ubiquitous soluble enzyme found in almost all animal species. A wide range of inducers, including oxidants and phenolic compounds, are highly effective in inducing NQO1 [3] . Utilizing NAD(P)H as an electron donor catalyzes two-electron reduction of quinones to hydroquinone. NQO1 binds and stabilizes several short-lived proteins, including the tumor suppressors p53 and p73 and the enzyme ornithine decarboxylase (ODC) [4] . NQO1 is present in almost all normal human tissues at different levels of expression. In general, adipocytes, vascular endothelium, and epithelial cells express it at high levels. Human hepatocytes and miocardia have lower levels of NQO1 expression [5, 6] . The NQO1 enzyme is a 273-amino-acid protein regulated by Nrf2 and the aryl hydrocarbon receptor and encoded by the NQO1 gene (AhR) [7] . Its function has been extensively researched. NQO1 has been studied extensively for its quinone reduction, significant antioxidant activity, reduction of ubiquinone and vitamin E derivatives to antioxidant forms, and superoxide scavenging [2] . Apart from its functions in disease models, NQO1 has also been linked to human cardiovascular diseases [8] . The multifunctionality of the NQO1 is represented in Figure 1 . NQO1 is a promising target for cancer detection, selective anticancer therapy, and provides multiple layers of protection to cells against carcinogenesis. NQO1 is involved in shielding cells from a range of harmful compounds, including quinones and other reactive oxygen species (ROS). Apart from this, it also plays a significant role in p53 stabilization [9] . This enzyme is bound to protect the cell's internal molecules and prevent detrimental changes that disturb the cell's homeostasis. NQO1 can provide several layers of protection to normal cells, allowing them to resist carcinogens [10] .

In cancer cells, it is over expressed, encouraging cell proliferation, malignant transformation, and drug resistance. Hence NQO1 acts as both a cancer suppressor and tumor promoter ( Figure 2 ) [11] . The high amount of NQO1 in cancer cells is thought to help them cope up with oxidative stress, just as they do in healthy cells. Studies of transcription factor Nrf2, which controls NQO1 expression, have partially supported this hypothesis. Gain-offunction mutations in Nrf2 or loss-of-function mutations in Keep over-activate Nrf2 in many cancers, including lung, pancreas, liver, gall bladder, and ovarian cancers [12] . Nrf2 gene hyperactivation helps malignant or transformed cells escape severe oxidative stress like over expression of NQO1. The mechanism by which NQO1 is over expressed via Nrf2 may vary between solid tumor types. For example, in gall bladder cancer, mutations in Keap1 cause the lowest binding with Nrf2 and drive the expression of NQO1. In contrast, in pancreatic cancer, K-ras mutations cause the lowest binding with Nrf2 and drive the expression of NQO1 [13] . Furthermore, Nrf2-induced over expression of NQO1 can play a significant role in chemotherapy failures, where it may be an adaptive response to oxidative stress and cytotoxicity and provide cancer cells with defense [14] . Therefore, as depicted in Figure 3 , inhibiting NQO1 would enable selective anticancer therapy for chemotherapy failures caused due to detoxification catalyzed by NQO1 [14] . Ayurveda, the Indian system of medicine, is one of the earliest systems of medical practice in health management and has played a vital role in providing health care service to human civilization from its inception. Medicinal plants are still the essential source of modern medicine. Additionally, the literature reveals that Indian traditional plants have high potent phytobioactive compounds for developing new drugs [15, 16] . The medical substances causing "a state of non-specifically increased resistance" of the organism (SNIR) were named "adaptogens". A plant-origin substance increases non-specific resistance [17, 18] . Development of phytobioactives that can move from the state of immune deficiency to normal condition would likely have a significant impact [19] .

The proposed study was primarily focused on quinones, but the chemical classes like flavones, curcumin, and coumarins were previously reported as the potent inhibitors for NQO1. The flavonoids are identified as a potent inhibitor for NQO1 through competitive inhibition of NAD(P)H [20] [21] [22] . The quinones and related molecules like flavones, terpenoids, coumarins from tulsi, garlic, turmeric, punarnava, and other various medicinal plants which have been potential anti-cancerous effects were short-listed for studying their plausible interaction with NQO1. Furthermore, the study was extended towards the selective phytobioactives with high specificity for cancer biology, and they are efficiently targeted to tumor tissues enhancing NQO1 [23] .

The inhibitors of NQO1 have shown promising outcomes in certain aspects where dicoumarol, a competitive inhibitor of NQO1, potentiates cisplatin-induced apoptosis in p53 wild-type urogenital cancer cell lines [24] . Meanwhile, a study has also revealed that β-lapachone from the bark of the lapacho tree affects the expression of NQO1 by mediating the inactivation of the Akt/mTOR pathway, resulting in significant anti-proliferation and anti-metastasis effects in breast cancer cell lines [25] . Based on this evidence, we hypothesize that inhibition of NQO1 will sensitize cancer cells to chemotherapeutic drugs. The proposed in silico work is geared towards screening, identification, and biological characterization of phytochemical inhibitors of NQO1 for enhancing the anticancer activity of chemotherapeutics. In the current study, we have identified the interactions of several Indian medicinal plants containing phytobioactives, including quinones with the different residues of NQO1, and the conformational changes imposed upon their binding by using the Molecular Docking technique. The potency of the phytobioactives was evaluated by MD simulation studies.

Medicinal plants rich in quinones, flavones, and terpenoids were noted and their phytoconstituents were shortlisted accordingly. A list of biologically phytobioactives is depicted in Table 1 . 

The selected ligands were downloaded from the NCBI, USA-PubChem chemistry database in three-dimensional form. The molecular docking software Argus Lab version 4.0.1 (http://www.arguslab.com/, (accessed on 11 August 2021)) was used to improve the geometric augmentation of the ligands. The two-dimensional and three-dimensional structures of prepared ligands are shown in Figure 4 and Table 2 . 

The three-dimensional Structure of the protein NQO1(PDB ID:2F1O) was retrieved from the Protein Data Bank (PDB). Furthermore, the non-standard amino acids bound to the downloaded NQO1 PDB file protein were removed or modified using Pymol software ( Figure 5 ). 

The binding pockets of NQO1(2F1O) protein-ligand binding were predicted using the in silico tool CASTp (http://sts.bioe.uic.edu/in, (accessed on 11 August 2021)).

The NQO1 (2F1O) protein structure was refined using the Mod Refiner server for protein refinement (https://zhanglab.ccmb.med.umich.edu/ModRefiner/, (accessed on 11 August 2021)). The Ramachandran plot was used to validate and evaluate the refined protein structures of NQO1, revealing that the energetically allowed protein structure of 2F1O regions for backbone dihedral angles toward amino acid residues were found. RAMPAGE was used to build the plots. The PROCHECK RAMPAGE results for the NQO1 revealed that its structure is stable, and the results are shown in Figure 6 and Table 3 . 

The prix version 0.8 open access docking program was used for the better understanding of molecular interaction and the docking between the NQO1 protein and phytobioactives (ligands) were uploaded. The PDB format NQO1 protein was selected, the ligands were uploaded, and the grid box was marked to shield the active site residues, ready to be preferred binding residues to achieve the maximum orientation with the lowest binding affinity (Kcal/mol) values.

The Ligplot+2.2 and the BIOVIA Discovery Studio Visualizer were used to visualize the docked conformation of the ligand against the NQO1 protein. The interactions like hydrogen bonds, hydrophobic interaction, and bond length were visualized using this program, including the NQO1 protein and a variety of plant-derived compounds with some naturally occurring quinones. The 3D Visualization was done with the BIOVIA Discovery Studio Visualizer, while the 2D interaction was done with Ligplot+2.2 [26] [27] [28] [29] .

In the present study, a molecular dynamics simulation was carried out on a 64-bit Ubuntu 20.04 platform, in a Dell Precision 7820 equipped with Intel Xeon Gold (20 core), 512 GB RAM, and 24 GB Quadro RTX-6000 Nvidia GPU. MDSs for Orientin were carried out against NQO1 proteins. The water model was inserted in the docked protein-ligand complex in an orthorhombic periodic border of the box under solvated conditions using a system-builder such as TIP3P (transferable intermolecular potential with three points). To neutralize the system, Na + ion (51.216 mM, with the charge of +31) and Cl − (56.173 mM, with a charge of −34) for NQO1 was used. This step automatically neutralizes the charge of the system during the study of the protein dynamics when the ligand is competing at the binding site [30, 31] . Furthermore, a molecular dynamics simulation was carried out under some periodic boundary conditions in the atom numbers, pressure, and temperature (NPT) ensemble, with the temperature set to 300 K and 1 atmospheric pressure, then relaxed using the Desmond program's default relaxation methodology. The simulation job took 50 nanoseconds to complete. RMSD (Root-mean-square deviation), RMSF (Rootmean-square fluctuation) and the total energy of complexes were analyzed by using event analysis and simulations-interaction diagrams [32] .

Pharmacokinetic and Toxicity (ADMET) profiles of identified phytobioactives from various medicinal plants were undertaken. It is generally established that poor ADMET (absorption, distribution, metabolism, excretion, and toxicity) qualities can degrade pharmacological activity. Furthermore, ADMET characteristics were examined using in silico methods to determine whether the screened phytobioactives would be good candidates for suitable medication. Unwanted pharmacokinetics and toxicity are practical causes of drug failure. This is expensive to discover at the clinical phase. The toxicity profile of all screened phytobioactives from various medicinal plants is based on AMES toxicity. Based on the bioavailability and drug-likeness of these three compounds, the results of more potent phytobioactives suitable for drug discovery are shown in Figure 7 and Table 4 . 

The molecular energy, electronic density, and orbital energies of a particular system, including the Highest Occupied Molecular Orbital (HOMO) and the Lowest Unoccupied Molecular Orbital (LUMO) were determined using the Kohn-Sham (KS) approach [33] [34] [35] [36] considering the CDFT or conceptual density functional theory variant of DFT [37] [38] [39] [40] [41] [42] [43] . The conformers of the compounds studied in this work were determined using MarvinView 17.15 from ChemAxon [http://www.chemaxon.com], (accessed on 15 August 2021) by using the entire MMFF94 force field to perform molecular mechanics calculations [44] [45] [46] [47] [48] . The Density Functional Tight Binding (DFTBA) methodology [49] was considered for geometry preoptimization and frequency calculation. This step was required to ensure that there were no imaginary frequencies, which is a usual test for the optimized structures' stability as a minimum within the energy surface. The estimation of the chemical reactivity descriptors of the studied ligands was accomplished using the MN12SX/Def2TZVP/H2O model chemistry [50] [51] [52] on the optimized at the same level molecular structures, as it has been shown that it fulfils the 'Koopmans in DFT' (KID) protocol [53] [54] [55] [56] [57] [58] [59] [60] [61] [62] [63] [64] [65] [66] [67] . Gaussian 16 [49] and the SMD solvent model [68] were considered for the determinations. This model chemistry is based on the application of the MN12SX density function [50] in connection to the Def2TZVP basis set [51, 52] being that the charge of the molecules is equal to zero and considering the corresponding negative and positive ions in the doublet spin state.

The NQO1 protein structure validation was examined using RAMPAGE. The initial validation was 92.4% of residues in a favorable region, and thus the protein could be subjected to further docking.

The consequences of this study can be deciphered from Figures 8 and 9 and, the bestdocked posture of the multitude of sub-atomic docked compounds was thought about, and the most reduced relating restricting liking was marked. These docked molecules were visualized and analyzed utilizing Ligplot+ V 2.2 and BIOVIA Discovery studio Visualizer software, highlighting the nearby labeled binding residues [69] . The NQO1 protein (2F1O) is seen sharing the hydrogen bonds, which are lower than 2.75 long, with semi-surrounded hydrophobic associations with the chosen molecules. 

Molecular docking is a commonly used approach in drug discovery for drug discovery with little or no adverse effects. It is a two-step process that begins with geometrical optimization of the ligand and target biomolecule. The conformations in the receptor-identified active region are then ranked according to their score, which varies from one software to the next depending on the algorithms used to develop them. Among the selected compounds, Orientin was found to be more potent against NQO1. All the listed compounds in Table 1 interacted with NQO1, but Orientin bound away from the coenzyme such as FAD binding to NQO1 (Figure 10) , resulting in the non-competitive type of inhibition. Orientin interacts with NQO1 via hydrogen bond with Arg272, Lys141, and plenty of water molecules present at Orientin's non-competitive bind site (Figures 10a,b) . These results implicate that Orientin binding with NQO1 is very strong as compared to other compounds (see Table S2 of the Supplementary Materials). Figure 11 shows that the two-Dimensional and three-Dimensional visualisation of the phytobioactives docked against the NQO1 (2F1O) protein exhibits an interaction, i.e., hydrogen bonding and other lower interactions like Van der Waals force, π − π stacked, π − π T-shaped, π-alkyl and carbon-hydrogen bond.

Using the Molecular Docking (in silico) technique, we analyzed the interaction between the NQO1 protein and a ligand molecule. Dicumarol is known as a potent (standard) inhibitory molecule for NQO1. The Dicumarol ( Figure 11A ) molecule (ligand) exhibits a binding affinity of −6.9 Kcal/mol and two hydrogen bonds with Phe 106 and Val 108 binding residues NQO1 protein, respectively. It also forms other interactions with the NQO1 protein. Similarly, melatonin ( Figure 11B ) exhibits a binding affinity of −5.6 Kcal/mol and forms two hydrogens bonding with Lue157 and Asp 266, respectively. Orientin ( Figure 11C ) shows the binding affinity of −6.6 Kcal/mol and forms two hydrogen bonds with the binding residues Gly52 and Tyr190. Trimethadione ( Figure 11D ) exhibits a binding affinity of −6 Kcal/mol and forms four hydrogen bonds with the binding residues Trp105, Trp105, Gly149, and Gly150. The binding to Gly150 is in accordance with previous results [27] . Also, in a recent study of the dual inhibitors NQO1 and GSTP1 (glutathione-S.transferase Pi1), MNPC was in alignment with our findings as far as some of the major amino acid residues are concerned [70] . 

To study the protein dynamics when the Orientin binds to NQO1, MDS studies were carried out to analyze the changes in protein during simulation for the docked proteinligand complex. The Desmond equilibrates the system to achieve a stable conformation if the initial structure was energetically unstable. Hence in the present study, we performed MDS for docked complexes of Orientin and NQO1 (Figure 12 ). The protein RMSD overlaps with ligand RMSD (orientin) in the initial stage and goes up to 50 ns. It shows that it forms multiple interactions with the amino acid residues at the active site (Figure 12b ). The type of interaction and number of the contact point is summarized in the pictorial diagram ( Figure 13 ). The critical amino acids which aid in forming interactions are Leu220, Val183, and Pro219, and they play a prominent role at the non-competitive binding site. The twodimensional binding geometry of Orientin with NQO1after MDSs shows that the Orientin interacts with the putative binding site of NQO1 with various interactions (Figures 13a-c) . The protein secondary structure elements (SSE) for orientin binding to NQO1 induces the fluctuation in protein structure, which causes 28.25%, and 11.63% changes in α-helix and β-strands throughout the simulation up to 50ns ( Figure 14) . The graph below summarizes the SSE composition for each orbital frame during simulation, and the graph at the bottom monitors each residue and its SSE assignment over time ( Figure 14) . Thus, MDS studies suggest that Orientin binding to NQO1 away from the substrate-binding site induces a potential conformational change in the substrate-binding site, thereby inhibiting substrate accessibility towards the FAD binding domain. 

The calculated global reactivity descriptors [37] [38] [39] [40] [41] [42] [43] , which were estimated following the methodology presented in the Section 2.10 together with the in-house developed CDFT software tool, are displayed in Table 5 . Because global hardness is a direct measure of electron density deformation and chemical reactivity, which is related to the HOMO-LUMO gap, it can be seen that Orientin will be the most reactive ligand, with Dicumarol and Melatonin being very similar in reactivity, and Trimethadione will be the least reactive of all the ligands considered. The electrodonating power EDP is more important than its electroaccepting EAP counterpart for all the ligands, which can be explained in terms of their molecular structures. However, when the values of EDP and EAP for each molecule are compared, it can be deduced that the Orientin and Dicumarol ligands will have considerably different reactivity than the other ligands. The electrophilicity ω index encompasses the equilibrium between an electrophile's tendency to acquire extra electron density and a molecule's resistance to exchanging electron density with the environment [71] . According to an electrophilicity ω scale for classifying organic molecules as strong, moderate, or marginal electrophiles (>1.5 eV for the first case, between 0.8 and 1.5 eV for the second case, and 0.8 eV for the last case) [72] [73] [74] and a review of Table 5 , all ligands can be classified as strong electrophiles with the exception of Trimethadione.

Local reactivity descriptors have been developed in addition to global reactivity descriptors to gain a sense of the changes in chemical reactivity across the atoms inside the molecule. The Fukui functions [37] [38] [39] and the dual descriptor [41, [75] [76] [77] [78] [79] are the most commonly used local reactivity descriptors. The NFF and the EFF are associated with the sites within a molecular system which are prone to nucleophilic or electrophilic attacks, respectively. Although the NFF and EFF have proven to be beneficial in identifying reactive sites, the dual descriptor DD is thought to describe the nucleophilic and electrophilic sites in a molecule clearly [79] . Graphical representations of the DD for the five studied ligands is displayed in Figure 15 showing the zones where DD > 0 and DD < 0. Although there is some overlap between the different sections inside the ligands, these graphical representations allow for a clear distinction between the locations within the molecules where the Dual Descriptor will be bigger or smaller than zero, signaling chemical reactivity differences.

In summary, the phytoactive compounds such as Orientin, Trimethadione, Alliin, and some other potent plant-derived molecules from a range of chemical classes has shown better interaction towards the NQO1 protein when compared to the standard NQO1 inhibitor Dicumarol. Understanding the complex mechanism and functioning of NQO1 in cancer studies reveals that this protein exhibits as both tumor suppressor and tumor promoter under different tools. The molecular docking and molecular dynamics studies revealed that the phytobioactive, Orientin, exhibited higher interaction with NQO1. The Orientin is a flavone molecule with an anticancer property that also includes anti-inflammation, neuroprotective, radiation protective, vasodilation, cardioprotective, antiviral, antibacterial, antidepressant-like antiadipogenesis, antinociceptive, and various antioxidant properties [80] . The results obtained from the current study conclude that the critical amino acids which aid in forming interactions are Leu220, Val183, and Pro219, which play a prominent role at the non-competitive binding site. The studies on flavonoids have implicated their potency as an antitumor agent. From this, we can hypothesize that using these phytobioactives can affect the expression of NQO1 in cancer cells. The biochemical properties and the mechanism of these phytochemical constituents can be studied and analyzed by in vitro and in vivo studies. In conclusion, the Indian Ayurvedic plants consist of various types of quinone molecules, which have a potency towards NQO1 inhibition. Furthermore, it would be interesting in the future to analyze the biological data through pharmacophore modeling and 3D QSAR studies to elucidate and substantiate the mechanism of action in comparison with the results of molecular docking and molecular dynamic studies considering the standard inhibitor, Dicumarol.

Supplementary Materials: The following are available online, Table S1 : List of some synthetic and semi-synthetic compounds screened against NQO1; Table S2 . Binding affinity and hydrogen bonding interaction of molecular docking analysis of phytobioactives against NQO1 (2F1O) Protein. Acknowledgments: The authors BS, CD, MVG, RRA and CS acknowledge the support and infrastructure provided by JSS AHER. SPK thank Amrita Vishwa Vidyapeetham for support extended towards the collaborations. NFH and DGM are researchers of CIMAV and CONACYT and want to thank both institutions for partial support. The authors extend their appreciation to the Researchers Supporting Project number RSP-2021/120, King Saud University, Riyadh, Saudi Arabia.

The authors declare no conflicts of interest.

NAD(P)H:quinone Acceptor Oxidoreductase 1 (NQO1), a Multifunctional Antioxidant Enzyme and Exceptionally Versatile Cytoprotector

Functions of NQO1 in Cellular Protection and CoQ10 Metabolism and its Potential Role as a Redox Sensitive Molecular Switch

Implications of NQO1 in Cancer Therapy

The Crystal Structure of NAD(P)H Quinone Oxidoreductase 1 in Complex with Its Potent Inhibitor Dicoumarol

Immunodetection of NAD(P)H:quinone Oxidoreductase 1 (NQO1) in Human Tissues. Free Radic

Immunohistochemical Detection of NAD(P)H:quinone Oxidoreductase in Human Lung and Lung Tumors

Antioxidant-induced Phosphorylation of Tyrosine 486 Leads to Rapid Nuclear Export of Bach1 That Allows Nrf2 to Bind to the Antioxidant Response Element and Activate Defensive Gene Expression

NAD(P)H:Quinone Oxidoreductase 1 and its Potential Protective Role in Cardiovascular Diseases and Related Conditions

Pro-and Anti-Apoptotic Effects of p53 in Cisplatin-treated Human Testicular Cancer are Cell Context-Dependent

Retraction Note: Disruption of NAD(P)H:quinone Oxidoreductase 1 Gene in Mice Leads to 20S Proteosomal Degradation of p63 Resulting in Thinning of Epithelium and Chemical-induced Skin Cancer

Roles of NAD (P) H-Quinone Oxidoreductase 1 (NQO1) On Cancer Progression and Chemoresistance

NAD(P)H:quinone oxidoreductase 1 (NQO1) in the Sensitivity and Resistance to Antitumor Quinones

Keap1 Loss Promotes Kras-driven Lung Cancer and Results in Dependence on Glutaminolysis

NAD(P)H:Quinone Oxidoreductase 1 (NQO1) as a Therapeutic and Diagnostic Target in Cancer

Potency of Extracts from Selected Egyptian Plants as Inducers of the Nrf2-dependent Chemopreventive Enzyme NQO1

Plant Adaptogens III. Earlier and More Recent Aspects and Concepts on their Mode of Action

New Substances of Plant Origin which Increase Nonspecific Resistance

Reconstitution of Immune Function in AIDS/ARC

Synthesis and Evaluation of 3-Aryloxymethyl-1, 2-dimethylindole-4, 7-diones as Mechanism-Based Inhibitors of NAD(P)H:Quinone Oxidoreductase 1 (NQO1) Activity

Coumarin-Based Inhibitors of Human NAD(P)H:Quinone Oxidoreductase-1. Identification, Structure-Activity, Off-Target Effects and In Vitro Human Pancreatic Cancer Toxicity

Inhibition of NAD(P)H:quinone Oxidoreductase 1 Activity and Induction of p53 Degradation by the Natural Phenolic Compound Curcumin

Immunoprotection by Botanical Drugs in Cancer Chemotherapy

Dicoumarol Potentiates Cisplatin-induced Apoptosis Mediated by c-Jun N-terminal Kinase in p53 Wild-type Urogenital Cancer Cell Lines

Effects of ES936, a Mechanism-Based Inhibitor of NAD(P)H:quinone Oxidoreductase 1, in Cellular Systems

Combined Molecular Modelling and 3D-QSAR Study for Understanding the Inhibition of NQO1 by Heterocyclic Quinone Derivatives

Negative Cooperativity in NAD(P)H Quinone Oxidoreductase 1 (NQO1)

NAD(P)H Quinone Oxidoreductase (NQO1): An Enzyme Which Needs Just Enough Mobility, in Just the Right Places

Functionalized Aurones as Inducers of NAD(P)H:Quinone Oxidoreductase 1 that Activate AhR/XRE and Nrf2/ARE Signaling Pathways: Synthesis, Evaluation and SAR

Elucidating the Role of Interacting Residues of the MSH2-MSH6 Complex in DNA Repair Mechanism: A Computational Approach

Molecular Dynamics Simulation (MDS) Analysis of Vibrio Cholerae ToxT Virulence Factor Complexed Docked Potential Inhib

In silico Prediction, Characterization, Molecular Docking, and Dynamic Studies on Fungal SDRs as Novel Targets for Searching Potential Fungicides Against Fusarium Wilt in Tomato

Computational Chemistry-Introduction to the Theory and Applications of Molecular and Quantum Mechanics

Computational Chemistry-A Practical Guide for Applying Techniques to Real-World Problems

Introduction to Computational Chemistry

Essentials of Computational Chemistry-Theories and Models

Density-Functional Theory of Atoms and Molecules

Chemical Reactivity Indexes in Density Functional Theory

Conceptual Density Functional Theory

Conceptual Density Functional Theory: Status, Prospects

Chemical Reactivity Theory-A Density Functional View

Conceptual Density Functional Theory Based Electronic Structure Principles

Merck Molecular Force Field. I. Basis, Form, Scope, Parameterization, and Performance of MMFF94

Merck Molecular Force Field. II. MMFF94 van der Waals and Electrostatic Parameters for Intermolecular Interactions

MMFF94s Option for Energy Minimization Studies

Merck Molecular Force Field. IV. Conformational Energies and Geometries for MMFF94

Merck Molecular Force field. V. Extension of MMFF94 Using Experimental Data, Additional Computational Data, and Empirical Rules

Screened-Exchange Density Functionals with Broad Accuracy for Chemistry and Solid-State Physics

Balanced Basis Sets of Split Valence, Triple Zeta Valence and Quadruple Zeta Valence Quality for H to Rn: Design and Assessment of Accuracy

Accurate Coulomb-fitting Basis Sets for H to R

Computational Peptidology Assisted by Conceptual Density Functional Theory for the Study of Five New Antifungal Tripeptides

Conceptual DFT as a Helpful Chemoinformatics Tool for the Study of the Clavanin Family of Antimicrobial Marine Peptides

Molecular Reactivity and Absorption Properties of Melanoidin Blue-G1 through Conceptual DFT

Conceptual DFT Study of the Local Chemical Reactivity of the Dilysyldipyrrolones A and B Intermediate Melanoidins

Conceptual DFT Study of the Local Chemical Reactivity of the Colored BISARG Melanoidin and Its Protonated Derivative

Computational Study of the Chemical Reactivity of the Blue-M1 Intermediate Melanoidin

Chemical Reactivity Theory Applied to the Calculation of the Local Reactivity Descriptors of a Colored Maillard Reaction Product

Blue M2: An Intermediate Melanoidin Studied via Conceptual DFT

Chemical-Reactivity Properties, Drug Likeness, and Bioactivity Scores of Seragamides A-F Anticancer Marine Peptides: Conceptual Density Functional Theory Viewpoint

Chemical Reactivity Theory and Empirical Bioactivity Scores as Computational Peptidology Alternative Tools for the Study of Two Anticancer Peptides of Marine Origin

Computational Prediction of Bioactivity Scores and Chemical Reactivity Properties of the Parasin I Therapeutic Peptide of Marine Origin Through the Calculation of Global and Local Conceptual DFT Descriptors

A Fast and Simple Evaluation of the Chemical Reactivity Properties of the Pristinamycin Family of Antimicrobial Peptides

Glossman-Mitnik, D. Conceptual DFT-Based Computational Peptidology of Marine Natural Compounds: Discodermins A-H

Virtual Screening of Marine Natural Compounds by Means of Chemoinformatics and CDFT-Based Computational Peptidology

Conceptual DFT as a Helpful Chemoinformatics Tool for the Study of the Clavanin Family of Antimicrobial Marine Peptides

Universal Solvation Model Based on Solute Electron Density and a Continuum Model of the Solvent Defined by the Bulk Dielectric Constant and Atomic Surface Tensions

Virtual Screening of Potential Phyto-Candidates as Therapeutic Leads Against SARS-CoV-2 Infection

Discovery of a Dual Inhibitor of NQO1 and GSTP1 for Treating Glioblastoma

Applications of the Conceptual Density Functional Theory Indices to Organic Chemistry Reactivity

Quantitative Characterization of the Global Electrophilicity Power of Common diene/Dienophile Pairs in Diels-Alder Reactions

Understanding the Mechanism of Polar Diels-Alder Reactions

Quantitative Characterization of the Global Electrophilicity Pattern of Some Reagents Involved in 1,3-Dipolar Cycloaddition Reactions

New Dual Descriptor for Chemical Reactivity

Theoretical Support for Using the ∆ f (r) Descriptor

Revisiting Caffeate's Capabilities as a Complexation Agent to Silver Cation in Mining Processes by means of the Dual Descriptor -A Conceptual DFT Approach

Explaining Reaction Mechanisms Using the Dual Descriptor: A Complementary Tool to the Molecular Electrostatic Potential

Why is the Dual Descriptor a More Accurate Local Reactivity Descriptor than Fukui Functions?

A Review on Medicinal Properties of Orientin