V. T. RAVIKUMAR

Bharathidasan University — India

Biochemistry, Genetics and Molecular Biology · Life Sciences

5h-index166citations19works0.02yr avg
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Research Topics

DNA and Nucleic Acid Chemistry(6), Asymmetric Synthesis and Catalysis(2), Advanced biosensing and bioanalysis techniques(2), RNA Interference and Gene Delivery(2), Chemical Synthesis and Analysis(2)

Publications19 total

Computational evaluation of berberine derivatives as potential modulators of TGF-β signalling in cancer
In Silico Pharmacology·2026Open Access
Pulmonary fibrosis in post-COVID-19: epithelial-mesenchymal transition as a key mechanism and target for therapy
Inflammopharmacology·2025
Dietary tannic acid attenuates elastase-induced pulmonary inflammation and emphysema in mice
Inflammopharmacology·2023· 10 cited
Correlative Studies Unravelling the Possible Mechanism of Cell Death in Tideglusib-Treated Human Ovarian Teratocarcinoma-Derived PA-1 Cells
Journal of Environmental Pathology Toxicology and Oncology·2017· 6 cited
Plant Isoquinoline Alkaloid Berberine Exhibits Chromatin Remodeling by Modulation of Histone Deacetylase To Induce Growth Arrest and Apoptosis in the A549 Cell Line
Journal of Agricultural and Food Chemistry·2016· 72 cited
Diagnostic Potential of Extracellular MicroRNA in Respiratory Diseases
Clinical Reviews in Allergy & Immunology·2016· 59 cited
ChemInform Abstract: Applications of Green Chemistry in the Manufacture of Oligonucleotide Drugs
ChemInform·2001
Special Issues for Synthetic Antisense Oligonucleotides
2000
ChemInform Abstract: 4‐Cyano‐2‐butenyl Group: A New Type of Protecting Group in Oligonucleotide Synthesis via Phosphoramidite Approach.
ChemInform·1998
Solution Phase Synthesis of an Oligodeoxyribonucleotide Phosphorothioate for Therapeutic Applications
Nucleosides and Nucleotides·1997
ChemInform Abstract: 4‐Cyano‐2‐butenyl Group: A New Type of Protecting Group in Oligonucleotide Synthesis via Phosphoramidite Approach.
ChemInform·1996
ChemInform Abstract: A Convenient Synthesis of Aryl Phosphorodichloridothioates Using Phase Transfer Catalyst.
ChemInform·1996
ChemInform Abstract: Phosphorothioates: β‐Fragmentation versus β‐Silicon Effect.
ChemInform·1996
ChemInform Abstract: A Mild Method for the Cleavage of Si‐C Bond in Oligonucleotide Synthesis
ChemInform·1995
ChemInform Abstract: A Convenient Large Scale Synthesis of N‐Boc‐Ethylenediamine.
ChemInform·1994
ChemInform Abstract: Stereocontrolled Ketene‐Imine Cycloaddition Reactions
ChemInform·1994· 14 cited
ChemInform Abstract: Hypervalent Iodine Oxidation of 5‐Substituted and 4,5‐Disubstituted Pyrazol‐3(2H)‐ones: A Facile Synthesis of Methyl 2‐Alkynoates (III) and Methyl 2,3‐Alkadienoates (V).
ChemInform·1989
ChemInform Abstract: Synthesis of A‐Homo Wieland‐Miescher Ketone: A Useful Building Block for Condensed Cycloheptanoid Natural Products.
Chemischer Informationsdienst·1986
Synthesis of A-Homo Wieland-Miescher Ketone: A Useful Building Block for Condensed Cycloheptanoid Natural Products
Synthesis·1985· 5 cited

Frequent Co-authors

Douglas L. Cole(5), S. Rajasekaran(3), Zacharia S. Cheruvallath(3), K. THANGARAJ(2), S. Swaminathan(2), K. Rajagopalan(2), Anthony N. Scozzari(2), A. KROTZ(2), Arunachalam Kalaiarasi(1), Chidambaram Anusha(1), Sankar Renu(1), Jayaraj John Marshal(1), Karthikeyan Muthusamy(1), Dhamotharan Pattarayan(1), Rajesh K. Thimmulappa(1), Gunda I. Georg(1), Nandhine Rajasekar(1), Deepa Gandhi(1), Ayyanar Sivanantham(1), Dharma Raj(1)