|Year : 2020 | Volume
| Issue : 68 | Page : 199-205
A bioinformatics-based investigation to screen and analyze the bioactivity of Piper longum Linn. compounds as a ground-breaking hostile to antidiabetic activity
Bikash Thakuria1, Sorforaj Laskar2, Samrat Adhikari2
1 Bioinformatics Centre, St. Edmund's College, Shillong 793003, Meghalaya, India
2 Department of Biotechnology, St. Edmund's College, Shillong 793003, Meghalaya, India
|Date of Submission||10-Sep-2019|
|Date of Decision||11-Nov-2019|
|Date of Web Publication||31-Mar-2020|
Department of Biotechnology, St. Edmund's College, Shillong - 793 003, Meghalaya
Source of Support: None, Conflict of Interest: None
| Abstract|| |
As of today, the utilization of herbal medicines has taken up the pace in treating diseases. This is due to the fact that they have lower risk of adverse reactions. Numerous plants are being used traditionally to treat various dreadful diseases including diabetes. Piper longum is one of the major and important medicinal plants in various systems of medicine, including the Ayurvedic system of medicine. Among the major bioactive compounds found in this plant, few compounds, viz., piperine, piperlongumine, piperlonguminine, and retrofractamide A, have been selected for studying the effectiveness on antidiabetic activity. An in silico approach was utilized to observe the major phytochemical properties and interaction studies of the constituents of P. longum, and finally, a pharmacophore investigation was carried out. In this study, we have observed the interaction of the four bioactive compounds taken from P. longum with the receptors via molecular docking technique. The binding of the ligands firmly with the receptors confirmed the fact that piperine, piperlongumine, piperlonguminine, and retrofractamide A act as inhibitors for dipeptidyl peptidase-4, GKRP, 11β-hydroxysteroid dehydrogenase type 1, glutamine-fructose-6-phosphate transaminase 1, and protein tyrosine phosphatase 1B, which encourage the glucose digestion and increment insulin affectability. The information acquired from this investigation might be taken further for in vitro examinations, which may, in the long run, be useful in recognizable proof of novel and successful particles. The outcomes acquired from this examination might provide strong understanding in the utility of phytochemicals against diabetes.
Keywords: Antidiabetic, bioactive compounds, molecular docking, pharmacophore, Piper longum
|How to cite this article:|
Thakuria B, Laskar S, Adhikari S. A bioinformatics-based investigation to screen and analyze the bioactivity of Piper longum Linn. compounds as a ground-breaking hostile to antidiabetic activity. Phcog Mag 2020;16, Suppl S1:199-205
|How to cite this URL:|
Thakuria B, Laskar S, Adhikari S. A bioinformatics-based investigation to screen and analyze the bioactivity of Piper longum Linn. compounds as a ground-breaking hostile to antidiabetic activity. Phcog Mag [serial online] 2020 [cited 2022 Sep 29];16, Suppl S1:199-205. Available from: http://www.phcog.com/text.asp?2020/16/68/199/281706
Abbreviations used: DPP-4: Dipeptidyl peptidase inhibitor 4; GKRP: Glucokinase regulatory protein; 11β-HSD1: 11β-Hydroxysteroid dehydrogenase type 1; GFPT1: Glutamine-fructose-6-phosphate transaminase 1; PTB1B: Protein tyrosine phosphatase 1B.
| Introduction|| |
Piper longum Linn., additionally called as long pepper, is one of the regular culinary herbs, which has been widely utilized as a constituent in different indigenous drugs. This long pepper has bioavailability upgrading action for some dietary substances and a few medications. The pharmacological properties of this plant additionally incorporate the antioxidant, mitigating, hostile to hyperlipidemic, against corpulence and hepatoprotective. Piperine, an alkaloid from Piper nigrum and P. longum, is a known inhibitor of different proteins in charge of biotransformation of medications. By restraining the digestion of medications, piperine improves the bioavailability of medications  which are hostile to diabetic action of the roots as likewise has been reported. Piperine in the blend with a sub-remedial portion of metformin has been reported for lowering blood glucose levels when contrasted with control gathering and furthermore demonstrated the more prominent bringing down of blood glucose  by other compounds alone or in a combination of piperine, piperlongumine, piperlonguminine, and retrofractamide A are recognized in P. longum. The detailed pharmacological exercises of piperlongumine incorporate cytotoxic, genotoxic, tumor enhancement, anti-angiogenic, anti-metastatic, anti-platelet conglomeration, antinociceptive, anxiolytic, energizer, prone to atherosclerotic, antidiabetic, antibacterial, hostile to contagious, leishmanicidal, trypanocidal, and schistosomicidal exercises. Piperlonguminine and retrofractamide A which essentially expanded the measure of adiponectin discharged into the medium just as the take-up of 2-deoxyglucose (DG) into the cells.
Diabetes mellitus (DM) is a heterogeneous gathering of metabolic infection described by constant hyperglycemia caused due to diminished insulin emission as well as expanded insulin obstruction. As opposed to type 1 diabetes that displays hyperglycemia and hypoinsulinemia, type 2 diabetes frequently show hyperglycemia and hyperinsulinemia. The mix of decreased glucose digestion and insulin obstruction prompts steady hyperglycemia in the fasting just as in the postprandial state. Patients with type 1 diabetes suffer from insulin insufficiency, inferable from the pancreatic β-cell disappointment, and insulin is an essential and viable treatment to bring down hyperglycemia. The element of type 2 DM (T2DM) is fractional or deficient in utilizing insulin even though synthetic insulin is accessible.
Numerous endeavors to make sense of the compelling medications for T2DM have been expanded. In the present decade, the pervasiveness of diabetes and its repeat and extreme reactions of chemotherapeutic medicines have prompted the resurgence of interests in the utilization of homegrown arrangements as increasingly viable medications with less or no symptoms. At present, inquire about on connection between hostile to diabetic bioactive mixes and T2DM has been very much distributed and archived.
In light of these confirmations, the goal of this examination is to distinguish antidiabetic properties of the selected bioactive compounds piperine, piperlongumine, piperlonguminine, and retrofractamide A recognized in P. longum by utilizing them as ligand against the five focused proteins: 11-β hydroxysteroid dehydrogenase type 1 (11β-HSD1), glutamine-fructose-6-phosphate transaminase 1 (GFPT1), protein-tyrosine phosphatase 1B, dipeptidyl peptidase-4 (DPP-4), and glucokinase administrative protein.
The receptor focuses for T2DM as detailed by numerous researchers to date are glycogen phosphorylase, protein tyrosine phosphate 1-beta, DPP-4, glucokinase, peroxisome proliferator enacted receptor-gamma, aldose reductase, insulin receptor, etc. 11β-HSD1 restraint is an enticing objective for the treatment of glucocorticoid-related infections, particularly T2DM. In fat tissue, inordinate cortisol generation through 11β-HSD1 movement has been linked with pathogenesis of T2DM and heftiness. Glutamine-fructose-6-phosphate amidotransferase (GFAT) or GFPT1 is the first and rate constraining protein of the hexosamine pathway. GFAT controls the motion of glucose into the hexosamine pathway and catalyzes the development of glucosamine-6-phosphate. Expanded GFPT1 or GFAT movement was connected to postprandial hyperglycemia, and this may speak to an early biochemical distortion in the normal history of T2DM. The hexosamine biosynthetic pathway is an elective pathway of glucose digestion that has, as of late, been involved in the pathogenesis of diabetic nephropathy. Therefore, this compound is a helpful objective against T2DM. Protein tyrosine phosphatase 1B (PTP1B) is a key individual from the family, a negative controller in insulin signal transduction, and a potential objective for the treatment of T2DM. DPP-4 inactivates glucagon-like peptide-1 which invigorates insulin emission and stifles glucagon discharge. Hence, DPP-4 inhibitors can go about as potential medication contender for T2DM. DPP-4 inhibitors, which have been generally utilized as remarkable blood glucose-subordinate enemy of diabetic specialists for patients with T2DM, show guarantee. GKRP (glucokinase administrative protein) shapes an inhibitory complex with glucokinase, the catalyst in charge of directing the take-up and capacity of dietary glucose. Along these lines, ligands that can go about as an inhibitor of GKRP will encourage the digestion of glucose in this manner bringing down hyperglycemia.
Docking procedure plans to foresee the exploratory restricting modes and affinities of little particles inside the coupling site of specific receptor targets and is presently utilized a standard computational instrument in medication structure for lead compound advancement and virtual screening concentrates to discover novel naturally available compounds. The docking device utilizes various calculations; the most prominently utilized is a genetic algorithm. Pharmacophore investigation is a clarification venture for docking results: low or high restricting liking of ligand to receptors. The target of this investigation was to distinguish the antidiabetic action of the four bioactive compounds present in P. longum as they have been contemplated in vivo and in vitro to have hostile to diabetic properties where the insulin-flagging and -related falls alongside protein articulation and action or potentially phosphorylation studies were considered yet did not have an in silico approach. Subsequently, the examination concentrates more on the in silico to check the setup certainty all the more absolutely.
| Methodology|| |
Three-dimensional (3D) structure of 11β-HSD1, GFPT1, protein tyrosine phosphatase 1B (PTB1B), DPP-4, and GKRP were taken from Protein Data Bank (PDB) as follows: 11β-HSD1 (PDB code 1XU7), GFPT1 (PDB code 2V4M), PTB1B (PDB code 3SME), DPP-4 (PDB code 1J2E), and GKRP (PDB code 4BBA). UCSF Chimera; Chimera 1.13.1rc  was used for visualization.
Bioactive compound preparation
All the bioactive compounds were downloaded from ChemSpider: Retrofractamide A (CID: 9188045), piperine (CID: 553590), piperlongumine (CID: 553441), and piperlonguminine (CID: 4478660). The 2D representations of all bioactive compounds were copied as SMILES format and converted to PDB format with 3D coordinates using Open Babel. UCSF Chimera 1.13.1rc was used for visualization. Ligands were checked for torsion count to detect currently active bonds with default settings.
The physicochemical properties of the four bioactive compounds had been retrieved from ChemSpider in the form of molecular formula, average mass, boiling point, hydrogen bond donor, hydrogen bond acceptor, freely rotating bonds, polar surface area, molar refractivity, monoisotopic mass, rule of five violations, and ACD/logP. [Table 1] represents the physicochemical properties.
|Table 1: Chemical and physical properties: Piperine, piperlongumine, piperlonguminine, and retrofractamide A|
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The bioactivity scores of all bioactive compounds were also calculated for different parameters, G protein-coupled receptor ligand activity, ion channel modulation, kinase inhibition activity, protease inhibitor, enzyme inhibitor, and nuclear receptor ligand activity. As we know for metal heterocyclic complexes, if the bioactivity score is more than 0.00, then the complex is active; however, if it is between −0.50 and 0.00, then the complex is moderately active, and if the complex has −0.50, then it is inactive. The potential bioactivity scores of all ligands are given in [Table 2], which indicates that all ligands show those properties which are required for the characteristics of ligand for acting as a drug. The data are obtained from the Molinspiration tool (predict bioactivity module).
|Table 2: Bioactivity scores of all bioactive compounds obtained from Molinspiration|
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Virtual screening by Lipinski's rule of five
Lipinski's rule of five  helps in distinguishing between drug-like and nondrug-like molecules. It predicts high probability of success or failure due to drug-likeness for molecules complying with two or more of the rules: molecular mass <500 Dalton, high lipophilicity (expressed as LogP <5), <5 hydrogen bond donors, less than 10 hydrogen bond acceptors, and molar refractivity between 40 and 130. This rule had been verified using the SCFBio drug designing tool named Sanjeevini.
Molecular docking studies were performed using offline AutoDockTools-1.5.6 on Windows platform. The AutoDockTools was used with the help of the MGL tools available. Lamarckian genetic algorithm was used to dock the four bioactive compounds: piperine, piperlongumine, piperlonguminine, and retrofractamide A against 11β-HSD1, GFPT1, protein-tyrosine phosphatase 1B, DPP-4, and glucokinase regulatory protein. The receptors were kept as a macromolecule and have been kept as rigid, and the ligands were kept flexible. The grid was enacted in such a way that the macromolecule and the ligands were submerged within the given grid parameters for all of the four ligands against the macromolecule.
Pharmacophore is an explanation step for the molecular docking result: low or high binding affinity of the ligand to receptors. This part of the process was carried out using the pharmacophore tool included in LigandScout. The program showed us the 2D and 3D structure of position and interaction of ligand in the binding pocket of the receptor. From these 2D figures, some types of the bond were identified by color. Three features namely hydrogen bond donor, hydrogen bond acceptor, aromatic interactions, and hydrophobic interactions were labeled.
| Results|| |
The physiochemical properties of the four bioactive compounds are referenced in [Table 1], which were all recovered from ChemSpider. Among the bioactive compounds, piperlongumine holds the maximum number of hydrogen bond acceptors and also the polar surface area of piperlongumine is the highest among the others. In terms of the monoisotopic mass, retrofractamide A and piperlongumine have higher masses than piperine and piperlonguminine. All the four bioactive compounds, namely piperine, piperlongumine, retrofractamide A, and piperlonguminine, do not violate the rule of five.
The bioactivity scores, which incorporate the GCPR ligand, particle channel modulator, kinase inhibitor, atomic receptor ligand, protease inhibitor, and compound inhibitor, are referenced in [Table 2].
Virtual screening by Lipinski's standard of five
The outcomes demonstrated that each of the four ligands passed Lipinski's standard of five and can go about as medication. The scores of all ligands are given in [Table 3]. All the four ligands taken show subatomic mass under 500 Da, high lipophilicity (communicated as LogP) under 5, under 5 hydrogen security contributors, under 10 hydrogen security acceptors, and molar refractivity between 40 and 130.
Subatomic docking of each of the five objective proteins or receptors 11β-HSD1, GFPT1, protein-tyrosine phosphatase 1B, DPP-4, and glucokinase administrative protein, with every one of the four ligands, piperine, retrofractamide A, piperlongumine, and piperlonguminine, was performed utilizing AutoDockTools, and 10 docking adaptations were created for every ligand. In any case, the conformer with the most astounding restricting vitality and least inhibition constant (Ki) has been accounted for. The parameters which have been accounted for in [Table 4] are restricting vitality, ligand effectiveness, hindrance consistent, intermolecular vitality, van der Waals HB-desolvation vitality, all-out interior vitality, torsional vitality, unbound vitality, clRMS, and refRMS. Therefore, the outcomes got in this examination plainly shows inhibition of receptors by the ligands, piperine, piperlongumine, piperlonguminine, and retrofractamide A (acting as inhibitors), which recommends that these inhibitors can follow up on DPP-4, GKRP, 11β-HSD1, GFPT1, and PTB1B, which will encourage glucose digestion and increment insulin affectability. The most astounding restricting vitality was seen in piperine with −8.96 kcal/mol pursued by retrofractamide A with −7.78 kcal/mol, piperlonguminine with −7.33 kcal/mol, and piperlongumine with −6.57 kcal/mol separately. Piperine additionally demonstrated the least hindrance steady (Ki) 0.429 μM showing the most grounded inhibitor of DPP-4. The docking adaptations which are spoken to in [Figure 1] indicate piperine and retrofractamide A complexed with DPP-4 and GKRP. This may be represented by the way that the bioactive mixes of P. longum have hostile to diabetic potential. Thus, from the coupling energies of all the four bioactive metabolites, piperine demonstrates the most astounding restricting fondness pursued by retrofractamide A, piperlonguminine, and piperlongumine. The chart of restricting vitality versus compliances has been created for all the four bioactive mixes and is spoken to in [Figure 2]. DPP-4 mainly interacts with ligands via hydrophobic bonds and hydrogen bond donor; GKRP interacts with mentioned ligands via hydrogen bond donor, hydrophobic bonds, and also hydrogen bond acceptors; 11β-HSD1 interacts with the ligands via hydrophobic bonds and hydrogen bond donor; GFPT1 and PTB1B interacts with the ligands via hydrophobic bonds, hydrogen bond acceptor along with aromatic bonds.
|Table 4: Depicting the various parameters of the docked receptors with various ligands (piperine, piperlongumine, piperlonguminine and retrofractamide A)|
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|Figure 1: Docked complexes of (a) piperine with dipeptidyl peptidase-4, (b) piperine with GKRP, (c) retrofractamide A with dipeptidyl peptidase-4, and (d) retrofractamide A with GKRP. The above complexes were prepared in AutoDock using Lamarckian genetic algorithm and were visualized in LigandScout|
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|Figure 2: Graph depicting the binding energy versus conformations (2.0 clustering) of (a) piperine and dipeptidyl peptidase-4, (b) piperine and GKRP, (c) retrofractamide A and dipeptidyl peptidase-4, and (d) retrofractamide A and GKRP|
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Inhibition constant (Ki)
The subatomic docking results demonstrate the restraint steady, which gives us an impression of the quality of docked ligand to go about as an inhibitor of the receptor. Piperine demonstrated the least hindrance steady 0.429 μM against DPP-4 trailed by retrofractamide A with 1.97 μM against GKRP (glucokinase administrative protein). The least hindrance steady of piperine and retrofractamide A approves their job as potential medication up-and-comer since restraints of DPP-4 and GKRP assume a job in glucose digestion consequently bringing down hyperglycemia. Furthermore, piperlongumine and piperlonguminine are the potential drug candidates, but the potential in piperine and retrofractamide A is more than the other two.
This progression clarifies the outcomes acquired from atomic docking. It likewise clarifies the high- and low-restricting fondness of ligands to receptors. Two ligands piperine and retrofractamide A and their collaboration with DPP-4 and GKRP were chosen for pharmacophore investigation as they indicated generally excellent docking scores. Pharmacophore examination appeared in [Figure 3] indicates two highlights in particular hydrogen bond contributor and hydrophobic connections. The outcomes unmistakably show the amino corrosive positions and their connections in this manner further approving the coupling partiality. [Figure 3] speaks to the pharmacophore investigation of piperine and retrofractamide A. [Table 5] demonstrates the amino corrosive positions and sort of collaborations of every bioactive compound.
|Figure 3: The pharmacophore analysis and amino acid positions of (a) piperine and dipeptidyl peptidase-4, (b) piperine and GKRP, (c) retrofractamide A and dipeptidyl peptidase-4, and (d) retrofractamide A and GKRP. The green dotted lines denote the hydrogen bond (donor); the yellow and the blue arcs denote the hydrophobic interactions among them|
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|Table 5: Pharmacophore analysis showing the amino acids interactions of all bioactive compounds along with their position, chain, and the type of interactions|
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| Discussion|| |
DM is one of the normal metabolic issues securing 2.8% of the total populace and is foreseen to cross 5.4% constantly by 2025. Hyperglycemia is regular in both T1DM and T2DM. T2DM is portrayed by insulin obstruction and weakened pancreatic β-cell work at the conclusion and dynamic β-cell brokenness after some time. Both T1DM and T2DM influence a large number of individuals all around the globe. Natural drugs have turned out to be unequivocally favored treatment to lessen the negative effect of DM and its extreme complexities because of lesser symptoms and minimal effort. In vivo and in vitro investigations of some major bioactive compounds have entrenched the connection of the bioactive compounds and their effort in bringing down hyperglycemia, along these lines being powerful against DM.In vitro and in vivo proof incorporates the impact on insulin-flagging and related falls in β-cells and so on. Furthermore, it influences as far as quality interpretation, protein articulation, movement, as well as phosphorylation. In any case, it comes up short on an in silico way to deal with distinguish major bioactive mixes and build up their job in bringing down hyperglycemia and improving insulin affectability. This can be accomplished by examining the association of the receptors and ligands employing subatomic docking and pharmacophore investigation draws near. As of late, a solid enemy of the hyperglycemic impact of P. longum on mice models has been accounted for, yet the activity instrument of its bioactive compounds has stayed obscure. The nearness of many plant optional metabolites makes P. longum a remedial center point, and subsequently, it requests an in silico way to deal with its restorative possibilities.
The subatomic docking approach accurately foresees and recognizes the greatest restricting method of a given ligand in the dynamic site or restricting pocket of a given protein and effectively rank a group of ligands in agreement to their relating tentatively decided restricting affinities. The pharmacophore examination clarifies the consequences of subatomic docking consequently further approving the coupling affinities along these lines supporting the in silico approach in building up of antidiabetic movement of bioactive compounds or ligands and foreseeing their job in bringing down hyperglycemia. Piperine and retrofractamide A demonstrated the least hindrance consistent 0.429 and 1.97 μM against DPP-4 and GKRP individually. This demonstrates their hindrance capacity to these receptors. In vivo examinations demonstrated that if both of these receptors can be repressed, high blood glucose levels can be limited. In this manner, the outcomes acquired in this examination obviously shows that restraint of receptors by the ligands piperine, piperlongumine, piperlonguminine, and retrofractamide A (acting as inhibitors) is upheld and further confirmed with the in vivo investigations,,,,,, which proposes that specific inhibitors can follow up on DPP-4, GKRP, 11β-HSD1, GFPT1, and PTB1B, which will encourage glucose digestion and increment insulin affectability. Individualistic approach for all the bioactive compounds mentioned here namely piperine, piperlongumine, piperlonguminine, and retrofractamide A can be further imposed and check for their more viable potentials against diabetes vehemently. If possible, then traditional and conventional approach for the use of these bioactive compounds in the plant shall be popularized not only in the rural areas but also in the suburban and urban areas too. P. longum is used in traditional medical practice in the Cook Islands wherein the leaves are pounded in a wooden bowl with little water and used to wash the chest of a person with suspected breast cancer. This application of P. longum to treat tumors is also recorded in Indian Ayurvedic medicine. P. longum is traditionally and internally used in Chinese medicine to treat stomach chills, vomiting, etc., while in Ayurvedic medicine, it is used to treat colds, asthma, bronchitis, etc.
| Conclusion|| |
All the four ligands piperine, retrofractamide A, piperlongumine, and piperlonguminine indicated great subatomic docking results which were additionally confirmed with the pharmacophore investigation. Piperine with −8.69 kcal/mol restricting vitality and 0.429 μM hindrance consistent demonstrated the greatest potential to be a decent inhibitor against focused receptors. Even though the essential ideas of connection among ligands and focused on receptors had been as of now characterized, numerous inquiries still stayed indistinct for connection between docking result in AutoDock step and number of bonds in 2D structure of pharmacophore examination step. In this way, further research is required utilizing molecular dynamics simulations and hydrogen bond examination to unmistakably comprehend the strength of hydrogen bonds and hydrophobic connections between bioactive mixes and focused on receptors.
The authors express their heartfelt gratitude to Dr. Sylvanus Lamare, Principal, St. Edmund's College, Shillong, along with Bro. Simon Coelho, Secretary, Governing body, St. Edmund's College, Shillong, for their immense support and encouragement throughout the work. We would also like to take the opportunity to acknowledge LigandScout for allowing us to utilize the software for certain period for pharmacophore module in the package.
Financial support and sponsorship
We take this opportunity to acknowledge the funding received from the Department of Biotechnology, Government of India, for setting up the Bioinformatics Centre, under BTISNET program, Shillong, with a sanction number BT/BI/25/001/2006 dated November 21, 2008.
Conflicts of interest
There are no conflicts of interest.
| References|| |
Dudhatra GB, Mody SK, Awale MM, Patel HB, Modi CM, Kumar A, et al
. A comprehensive review on pharmacotherapeutics of herbal bioenhancers. ScientificWorldJournal 2012;2012:637953.
Choudhary N, Singh V. A census of P. longum's
phytochemicals and their network pharmacological evaluation for identifying novel drug-like molecules against various diseases, with a special focus on neurological disorders. PLoS One 2018;13:e0191006.
Sama V, Nadipelli M, Yenumula P, Bommineni MR, Mullangi R. Effect of piperine on antihyperglycemic activity and pharmacokinetic profile of nateglinide. Arzneimittelforschung 2012;62:384-8.
Atal S, Atal S, Vyas S, Phadnis P. Bio-enhancing effect of piperine with metformin on lowering blood glucose level in alloxan induced diabetic mice. Pharmacognosy Res 2016;8:56-60.
Hammad AS, Ravindran S, Khalil A, Munusamy S. Structure-activity relationship of piperine and its synthetic amide analogs for therapeutic potential to prevent experimentally induced ER stress in vitro
. Cell Stress Chaperones 2017;22:417-28.
Matsuda H, Nakamura S, Yoshikawa M. Search for new type of PPARγ agonist-like anti-diabetic compounds from medicinal plants. Biol Pharm Bull 2014;37:884-91.
Islam MA, Bhayye S, Adeniyi AA, Soliman ME, Pillay TS. Diabetes mellitus caused by mutations in human insulin: Analysis of impaired receptor binding of insulins Wakayama, Los Angeles and Chicago using pharmacoinformatics. J Biomol Struct Dyn 2017;35:724-37.
Ye J. Mechanisms of insulin resistance in obesity. Front Med 2013;7:14-24.
Westley RL, May FE. A twenty- first century cancer epidemic caused by obesity: The involvement of insulin, diabetes, and insulin-like growth factors. Int J Endocrinol 2013;2013:632461.
Guo S. Insulin signaling, resistance, and the metabolic syndrome: Insights from mouse models into disease mechanisms. J Endocrinol 2014;220:T1-23.
Nguyen Vo TH, Tran N, Nguyen D, Le L. An in silico
study on antidiabetic activity of bioactive compounds in Euphorbia thymifolia Linn. Springerplus 2016;5:1359.
Kaushik P, Lal Khokra S, Rana AC, Kaushik D. Pharmacophore modeling and molecular docking studies on Pinus roxburghii
as a target for diabetes mellitus. Adv Bioinformatics 2014;2014:903246.
Hosfield DJ, Wu Y, Skene RJ, Hilgers M, Jennings A, Snell GP, et al
. Conformational flexibility in crystal structures of human 11beta-hydroxysteroid dehydrogenase type I provide insights into glucocorticoid interconversion and enzyme regulation. J Biol Chem 2005;280:4639-48.
Srinivasan V, Sandhya N, Sampathkumar R, Farooq S, Mohan V, Balasubramanyam M. Glutamine fructose-6-phosphate amidotransferase (GFAT) gene expression and activity in patients with type 2 diabetes: Inter-relationships with hyperglycaemia and oxidative stress. Clin Biochem 2007;40:952-7.
Ng DP, Walker WH, Chia KS, Choo S, Warram JH, Krolewski AS. Scrutiny of the glutamine-fructose-6-phosphate transaminase 1 (GFPT1) locus reveals conserved haplotype block structure not associated with diabetic nephropathy. Diabetes 2004;53:865-9.
Sun J, Qu C, Wang Y, Huang H, Zhang M, Li H, et al
. PTP1B, A potential target of type 2 diabetes mellitus. Mol Biol 2016;5:174.
Dar AM, Khan MA, Mir S, Gatoo MA. DNA binding, cleavage activity, molecular docking, cytotoxicity and genotoxicity studies of newly synthesized copper based metal complexes. Pharm Anal Acta 2016;7:1636-16.
Raimondo A, Rees MG, Gloyn AL. Glucokinase regulatory protein: Complexity at the crossroads of triglyceride and glucose metabolism. Curr Opin Lipidol 2015;26:88-95.
Guedes IA, de Magalhães CS, Dardenne LE. Receptor-ligand molecular docking. Biophys Rev 2014;6:75-87.
Berman HM, Westbrook J, Feng Z, Gilliland G, Bhat TN, Weissig H, et al
. The protein data bank. Nucleic Acids Res 2000;28:235-42.
Pettersen EF, Goddard TD, Huang CC, Couch GS, Greenblatt DM, Meng EC, et al
. UCSF Chimera-a visualization system for exploratory research and analysis. J Comput Chem 2004;25:1605-12.
Ayers M. ChemSpider: The free chemical database. Ref Rev 2012;26:45-6.
O'Boyle NM, Banck M, James CA, Morley C, Vandermeersch T, Hutchison GR. Open Babel: An open chemical toolbox. J Cheminform 2011;3:33.
Lipinski CA. Lead- and drug-like compounds: The rule-of-five revolution. Drug Discov Today Technol 2004;1:337-41.
Jayaram B, Singh T, Mukherjee G, Mathur A, Shekhar S, Shekhar V. Sanjeevini: A freely accessible web-server for target directed lead molecule discovery. BMC Bioinformatics 2012;13 Suppl 17:S7.
Morris GM, Huey R, Lindstrom W, Sanner MF, Belew RK, Goodsell DS, et al
. AutoDock4 and AutoDockTools4: Automated docking with selective receptor flexibility. J Comput Chem 2009;30:2785-91.
Wolber G, Langer T. LigandScout: 3-D pharmacophores derived from protein-bound ligands and their use as virtual screening filters. J Chem Inf Model 2005;45:160-9.
Patel DK, Prasad SK, Kumar R, Hemalatha S. An overview on antidiabetic medicinal plants having insulin mimetic property. Asian Pac J Trop Biomed 2012;2:320-30.
Donner T, Muñoz M. Update on insulin therapy for type 2 diabetes. J Clin Endocrinol Metab 2012;97:1405-13.
Christodoulou MI, Tchoumtchoua J, Skaltsounis AL, Scorilas A, Halabalaki M. Natural alkaloids intervening the insulin pathway: New hopes for anti-diabetic agents? Curr Med Chem 2012;25:1-33.
Tripathi A, Bankaitis VA. Molecular Docking: From Lock and Key to Combination Lock. J Mol Med Clin Appl 2017;2.
Wang Q, Long M, Qu H, Shen R, Zhang R, Xu J, et al
. DPP-4 inhibitors as treatments for type 1 diabetes mellitus: A systematic review and meta-analysis. J Diabetes Res 2018;2018:5308582.
Agius L. New hepatic targets for glycaemic control in diabetes. Best Pract Res Clin Endocrinol Metab 2007;21:587-605.
Dicker D. DPP-4 inhibitors: Impact on glycemic control and cardiovascular risk factors. Diabetes Care 2011;34 Suppl 2:S276-8.
Röhrborn D, Wronkowitz N, Eckel J. DPP4 in diabetes. Front Immunol 2015;6:386.
Zhang S, Zhang ZY. PTP1B as a drug target: Recent developments in PTP1B inhibitor discovery. Drug Discov Today 2007;12:373-81.
Nguyen ND, Le LT. Targeted proteins for diabetes drug design. Adv Nat Sci Nanosci Nanotech 2012;3:013001.
[Figure 1], [Figure 2], [Figure 3]
[Table 1], [Table 2], [Table 3], [Table 4], [Table 5]
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