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Bhavya, N. R. and Madegowda, M. and Neelufar and Ananda, S. and Javarappa, R. and Nagaraja, N. (2025) A multi-ion detection Schiff base chemosensor: turn-off and ratiometric fluorescence sensing of Ni2+, Co2+, Cd2+, and Cu2+ions. Journal of Molecular Structure, 1337. ISSN 0022-2860
Harish, K. K. and Khamees, H. A. and Venkatesha, K. and Nagaraja, O. and Madegowda, M. (2025) The pivotal role of the carbonyl group in methoxy chalcones: comprehensive analyses of the structure and computational insights into binding affinity towards monoamine oxidase enzymes. Molecular Systems Design & Engineering, 10 (4). ISSN 2058-9689
Revanna, B. N. and Madegowda, M. (2021) Dithiane based boronic acid as a carbohydrate sensor in an aqueous solution at pH 7.5: theoretical and experimental approach. Journal of Fluorescence, 31 (6). pp. 1683-1703.
Swamy Savvemala Girimanchanaika and Dukanya, D. and Swamynayaka, A. and Divya, G. and Madegowda, M. and Ganga, P. and Rangappa, K. S. and Vijay Pandey and Lobie, P. E. and Basappa (2021) Investigation of npb analogs that target phosphorylation of bad-ser99 in human mammary carcinoma cells. International Journal of Molecular Sciences, 22 (20). pp. 1-16.
Shamala, D. and Shivashankara, K. and Chandra and Madegowda, M. (2016) Synthesis of N1 and N2 coumarin substituted 1,2,3-triazole isomers via click chemistry approach. Synthetic Communications, 46 (5). pp. 433-441.
Srinivas, V. and Mohan, C. D. and Baburajeev, C. P. and Rangappa, S. and Jagadish, S. and Fuchs, J. E. and Sukhorukov, A. Yu. and Chandra and Mason, D. J. and Kumar, K. S. S. and Madegowda, M. and Bender, A. and Basappa and Rangappa, K. S. (2015) Synthesis and characterization of novel oxazines and demonstration that they specifically target cyclooxygenase 2. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 25 (15). pp. 2931-2936. ISSN 1464-3405
Ningaiah, S. and Doddaramappa, S. D. and Chandra and Madegowda, M. and Keshavamurthy, S. and Bhadraiah, U. K. (2014) One-pot tandem synthesis of tetrasubstituted pyrazoles via 1,3-dipolar cycloaddition between aryl hydrazones and ethyl but-2-ynoate. Synthetic Communications, 44 (15). pp. 2222-2231.
