Abstract
Background: Because of their biological properties, phytochemicals have been essential to nutraceutical treatment for diabetes mellitus. Various phytoconstituents derived from Tinospora are reported to have immunomodulatory, anti-arthritis, antioxidant, anti-allergic cardio, and oxidatively- induced stress protection.
Objectives: This study aimed to identify and characterize the key phytoconstituents of Tinospora cordifolia for their anti-inhibitory effects against α-amylase and α-glucosidase enzymes in controlling carbohydrate metabolism and potential drug molecule against Type II Diabetes Mellitus.
Methods: Based upon the literature survey, various compounds of T. cardiofolia were deduced from Pubchem and protein structure from the protein data bank. Virtual screening used Pyrx with α- amylase and α- glucosidase. Compounds with the highest binding affinity score and 3-d interaction analysis were used to identify the potential inhibitors among various compounds. Pharmacokinetic studies for drug likeliness and toxicity properties were characterized using SWISS ADME and ADMETSAR webservers.
Results: Based on their docking scores and binding affinities,, the biologically active compounds from T. cardifolia viz were observed. Isocolumbin, cordifoliside B, β-sitosterol, ecdysone, palmitoside E, Columbin and cordifoliside C interact with the active site amino acids of both the enzymes. Drug-likeness and pharmacophore studies showed that potential anti α- amylase and α- glucosidase inhibitors.
Conclusion: The compounds' efficacy of the screened phytoconstituents from T.cardifolia as prospective therapeutic candidates can be due to their great affinity for the enzymes' catalytic region, which can cause a conformation change and result in a reduction in enzyme activity. This study's findings might indicate a way to create a new class of drugs.
Graphical Abstract
[http://dx.doi.org/10.3390/molecules21050559] [PMID: 27136524]
[http://dx.doi.org/10.3390/molecules25020309] [PMID: 31940923]
[http://dx.doi.org/10.1039/C7FO00220C] [PMID: 28470323]
[http://dx.doi.org/10.3390/ijms19010004] [PMID: 29267214]
[http://dx.doi.org/10.2337/dc21-S002] [PMID: 33298413]
[http://dx.doi.org/10.1210/rp.56.1.69] [PMID: 11237226]
[http://dx.doi.org/10.1038/emm.2016.6] [PMID: 26964835]
[http://dx.doi.org/10.1007/s11101-021-09773-1] [PMID: 34421444]
[http://dx.doi.org/10.1016/j.lwt.2021.112455]
[http://dx.doi.org/10.1016/j.arabjc.2021.103381]
[http://dx.doi.org/10.1016/j.tifs.2021.10.003]
[http://dx.doi.org/10.1080/19390211.2021.1873214] [PMID: 33480818]
[http://dx.doi.org/10.1016/j.jep.2014.01.031] [PMID: 24556222]
[http://dx.doi.org/10.1016/S1674-8301(11)60038-9] [PMID: 23554702]
[http://dx.doi.org/10.1016/j.jep.2021.114540] [PMID: 34509604]
[http://dx.doi.org/10.1093/nar/gky1033] [PMID: 30371825]
[PMID: 19499576]
[http://dx.doi.org/10.1093/nar/gky380] [PMID: 29750256]
[http://dx.doi.org/10.1007/978-1-4939-2269-7_19]
[http://dx.doi.org/10.1016/S0169-409X(00)00129-0] [PMID: 11259830]
[http://dx.doi.org/10.1038/srep42717] [PMID: 28256516]
[http://dx.doi.org/10.1093/nar/gkab255] [PMID: 33893803]
[http://dx.doi.org/10.3390/biom9100551] [PMID: 31575072]
[http://dx.doi.org/10.1155/2015/824683]
[http://dx.doi.org/10.1021/acsomega.0c01622] [PMID: 32832761]
[http://dx.doi.org/10.1042/bj3460201] [PMID: 10657258]
[http://dx.doi.org/10.1107/S139900471500721X] [PMID: 26057678]
[http://dx.doi.org/10.1007/978-981-15-8791-7_10]
[http://dx.doi.org/10.2478/s11756-020-00575-y]
[http://dx.doi.org/10.1155/2021/7872406]
[http://dx.doi.org/10.1016/j.joim.2020.10.003] [PMID: 33071211]
[http://dx.doi.org/10.1007/s13596-020-00426-w]
[http://dx.doi.org/10.1038/s41573-020-00114-z] [PMID: 33510482]
[http://dx.doi.org/10.1016/j.cbpa.2008.03.016] [PMID: 18423384]
[http://dx.doi.org/10.3390/molecules27082398] [PMID: 35458596]