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BioImpacts. 2021;11(3): 187-197. doi: 10.34172/bi.2021.09
PMID: 34336607        PMCID: PMC8314033

Original Research

Characterization of isolated compounds from Morus spp. and their biological activity as anticancer molecules

Aditya Rao Rao Shimoga Janakirama 1,2 * ORCID, Suma Mathad Shivayogi 1, Jamuna Kolkar Satyanarayana 1, Ramesh Chapeyil Kumaran 1

Cited by CrossRef: 13

1- Siddappa R, Aditya Rao S, Usha B, Verma B, Mahadevappa P. Anti-proliferative Activity of Labdane Diterpenes Isolated from Polyalthia cerasoides and their Molecular Interaction Studies. CDDT. 2022;19(5) [Crossref]
2- Lahmidi S, Anouar E, Mortada S, El Hafi M, My El Abbes F, Essassi E, Mague J. Synthesis, structural characterization, antioxidant and antidiabetic activities, DFT calculation, and molecular docking of novel substituted phenolic and heterocyclic compounds. Journal of Biomolecular Structure and Dynamics. 2023;41(9):4167 [Crossref]
3- Gorjian H, Raftani Amiri Z, Mohammadzadeh Milani J, Ghaffari Khaligh N. Influence of Nanovesicle Type, Nanoliposome and Nanoniosome, on Antioxidant and Antimicrobial Activities of Encapsulated Myrtle Extract: A Comparative Study. Food Bioprocess Technol. 2022;15(1):144 [Crossref]
4- Shetty N, Prabhakaran M, Srivastava A. Pleiotropic nature of curcumin in targeting multiple apoptotic‐mediated factors and related strategies to treat gastric cancer: A review. Phytotherapy Research. 2021;35(10):5397 [Crossref]
5- Maqsood M, Anam Saeed R, Sahar A, Khan M. Mulberry plant as a source of functional food with therapeutic and nutritional applications: A review. Journal of Food Biochemistry. 2022;46(11) [Crossref]
6- Sukanya S, Venkatesh T, Rao S, Shivakumara N, Joy M. Facile synthesis of some 5-(3-substituted-thiophene)-pyrimidine derivatives and their pharmacological and computational studies. ChimTechActa. 2021;8(4) [Crossref]
7- Sukanya S, Venkatesh T, Shanavaz H. Synthesis of novel 5-[3-(4-chlorophenyl)-substituted-1,3-dimethylpyrimidine-2,4,6(1 H ,3 H ,5 H )-trione derivatives as potential anti-diabetic and anticancer agents . Nucleosides, Nucleotides & Nucleic Acids. 2023;:1 [Crossref]
8- KP A, Shimoga Janakirama A, Martin A. SIRT1 activation by Taurine: in vitro evaluation, molecular docking and molecular dynamics simulation studies. The Journal of Nutritional Biochemistry. 2022;102:108948 [Crossref]
9- Ji J, Wang K, Meng X, Zhong H, Li X, Zhao H, Xie G, Xie Y, Wang X, Zhu X. Elaiophylin Inhibits Tumorigenesis of Human Lung Adenocarcinoma by Inhibiting Mitophagy via Suppression of SIRT1/Nrf2 Signaling. Cancers. 2022;14(23):5812 [Crossref]
10- Selvan G T, Ashok A, Rao S. J A, Gollapalli P, R V, N S, Chaudhury N. Nrf2-regulated antioxidant response ameliorating ionizing radiation-induced damages explored throughin vitroand molecular dynamics simulations. Journal of Biomolecular Structure and Dynamics. 2023;41(17):8472 [Crossref]
11- Jaber Q, Shentaif A, Almajidi M, Ahmad I, Patel H, Azad A, Alnasser S, Alatawi H, Menaa F, Alfaifi S, Rahman M, Ali M, Rao S. Synthesis, Structure, and In Vitro Pharmacological Evaluation of some New Pyrimidine-2-Sulfonamide Derivatives and Their Molecular Docking Studies on Human Estrogen Receptor Alpha and CDK2/Cyclin Proteins. Russ J Bioorg Chem. 2023;49(S1):S106 [Crossref]
12- Kaswan P. Natural resources as cancer-treating material. South African Journal of Botany. 2023;158:369 [Crossref]
13- Rao S, Shetty N. Structure-based screening of natural product libraries in search of potential antiviral drug-leads as first-line treatment to COVID-19 infection. Microbial Pathogenesis. 2022;165:105497 [Crossref]
14- Rao A, Gollapalli P, Shetty N. Gene expression profile analysis unravelled the systems level association of renal cell carcinoma with diabetic nephropathy and Matrix-metalloproteinase-9 as a potential therapeutic target. Journal of Biomolecular Structure and Dynamics. 2023;41(16):7535 [Crossref]

As a peer-reviewed international open-access journal, BioImpacts publishes articles on basic and translational aspects of pharmaceutical and biomedical sciences. 
Acceptance rate: 24% 
Publication fee: Free of charge