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Rajendra Wudayagiri

Researcher at Sri Venkateswara University

Publications -  29
Citations -  491

Rajendra Wudayagiri is an academic researcher from Sri Venkateswara University. The author has contributed to research in topics: Docking (molecular) & Glutathione reductase. The author has an hindex of 10, co-authored 29 publications receiving 355 citations.

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Cervical cancer: Biomarkers for diagnosis and treatment.

TL;DR: The present review explains the currently available biomarkers for cervical cancer diagnosis and prognosis and strategies for the development of biomarkers based on cellular and molecular approaches such as DNA, protein and other metabolic markers with suitable clinical examples.
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Design, synthesis, anticancer, antimicrobial activities and molecular docking studies of theophylline containing acetylenes and theophylline containing 1,2,3-triazoles with variant nucleoside derivatives.

TL;DR: The docking studies demonstrate that compound 27, 28, 29 and 30 have good dock score and binding affinities with various therapeutic targets in cancer cell proliferation and these compounds have shown acceptable correlation with bioassay results in the regression plots generated in 2D QSAR models.
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Design, synthesis, anticancer activity and docking studies of theophylline containing 1,2,3-triazoles with variant amide derivatives

TL;DR: In vitro results demonstrate that compounds 22, 27, 36 and 40 have pivotal anticancer activity; among these, compounds 22 and 27 have significant cytotoxic activity in all three cell lines; the in silico docking studies reveal that compounds22, 27 and 36 have good dock scores, binding affinities and binding energies towards human epidermal growth factor receptor 2.
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Antimicrobial activity of Lactobacillus against microbial flora of cervicovaginal infections

TL;DR: Assessment of the probiotic nature of Lactobacillus in preventing cervical pathogens by studying the effectiveness of antimicrobial activity against vaginal pathogens.
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In silico molecular docking and in vitro antioxidant activity studies of novel α-aminophosphonates bearing 6-amino-1,3-dimethyl uracil.

TL;DR: Among the synthesized bioactive molecules, 4a, 4d, 4g, and 4h exhibited promising antioxidant activity compared with the standard drug Ascorbic acid, and molecular docking studies were performed against Aromatase enzyme for four compounds to support the biological results of the compounds.