Journal Articles

                For the complete list of publications, Check the following links

List of Publications: (in reverse chronological order) 

19. Green synthesis, characterization, linear and nonlinear optical properties of copper oxide nanoparticles using Senna auriculata leaf extract . S. D. A. Sujitha, A. G. B. Dileepan, G. Murali, N. Arumugam, A. I. Almansour, K. Sudarshan, S. Jeyaram, Spectrosc. Lett.  2025, DOI: 10.1080/00387010.2025.2523996

18. Nonlinear optical features of phenol red dye in different solvent media using Z-scan and density functional theory. B. Anusha, A. G. B. Dileepan, R. Ramasamy, R. V. Solomon, N. Arumugam, A. I. Almansour, K. Sudarshan, S. Jeyaram, J. Fluoresc.  2025, DOI: 10.1007/s10895-025-04224-y 

17. Bio-mediated green synthesis of copper oxide nanoparticles using plant extract and its applications to optical switching in nonlinear optics. R. Ariyamuthu, G. Murali, N. Arumugam, A. I. Almansour, K. Sudarshan, S. Jeyaram, Part. Sci. Technol. 2025, DOI: 10.1080/02726351.2025.2473527

16. Observation of fascinating nonlinear optical features of fluorescent dye in selected polar solvents by Z-scan and DFT method. K. Priyadharsini, A. G. B. Dileepan, R. Ramasamy, R. V. Solomon, N. Arumugam, A. I. Almansour, K. Sudarshan, S. Jeyaram, J. Fluoresc. 2025, DOI: 10.1007/s10895-025-04208-y 

15. DFT and Z-scan studies for the determination of nonlinear optical susceptibility and second order hyperpolarizability of ethidium bromide dye in different solvents. C. Deepa, A. G. B. Dileepan, R. Ramasamy, R. V. Solomon, N. Arumugam, A. I. Almansour, K. Sudarshan, S. Jeyaram, J. Fluoresc. 2025, DOI: 10.1007/s10895-025-04164-7

14. Newly green synthesized ZnO nanoparticles and their effective influence on photocatalytic and anti-microbial activities. M. Rathaiah, B. Venkataramana, K. Sudarshan, B. V. K. Naidu, ChemistrySelect 2025, DOI:  10.1002/slct.202406149 

13. Use of a universal CAR-T cell to simultaneously kill cancer cells and cancer associated fibroblasts. B. Huang, S. Zheng, K. Sudarshan, R. Mukkamala, M. Srinivasarao, T. Sardesai, X. Yang, H. Chu, P. S. Low, Front. Immunol. 2025, DOI: 10.3389/fimmu.2025.1539265 

12. Recent advances in the synthesis of diarylheptanoids. K.Sudarshan, S. Yarlagadda, S. Gupta, Chem. Asian J. 2024, e202400380. DOI: 10.1002/asia.202400380

11. Selective targeting of chemically modified miR-34a to prostate cancer using a small molecule ligand and an endosomal escape agent. A.   M. Abdelaal, I. S. Sohal, S. Iyer, K. Sudarshan, E. A. Orellana, K. E.  Ozcan, A. P. Santos, P. S. Low, A. L. Kasinski, Mol. Ther. Nucleic Acids, 2024, 102193. DOI: 10.1016/j.otmn.2024.102193

10. Developing folate-conjugated miR-34a therapeutic for prostate cancer treatment: Challenges and  promises. W. Li, Y. Wang, X. Liu, S. Wu, M. Wang, S. G. Turowski,  J. A. Spernyak,  A. Tracz, A. M. Abdelaal, K. Sudarshan, I. Puzanov, G. Chatta, A. L. Kasinski, D. G. Tang, Int. J. Mol. Sci.  , 2024, DOI: 10.3390/ijms25042123 

9. A first-in-class fully modified version of miR-34a with outstanding stability, activity, antitumor efficacy. A. M. Abdelaal, I. S. Sohal, S. Iyer, K. Sudarshan, H. Kothandaraman, N. A. Lanman, P. S. Low, A. L. Kasinski, Oncogene, 2023, 42, 2985-2999. DOI: 10.1038/s41388023-02801-8

8. Development of a simple high-throughput assay for directed evolution of enantioselective sulfoxide reductases. V. Tarallo, K. Sudarshan, V. Nosek, J. Misek, Chem. Commun. 2020, 56, 5386-5388. DOI: 10.1039/d0cc01660h

7. Regulation of mRNA translation by a photo riboswitch, K. A. Rotstan, M. M. Abdelsayed, L. F. Passalacqua, F. Chizzolini, K. Sudarshan, A. R. Chamberlin, J. Misek, A. Luptak, Elife, 2020, 9, e51737. DOI:10.7554/elife.51737

6. Discovery of a Isocoumarin analogue that modulates neuronal functions via neurotrophin receptor TrkB, K. Sudarshan, B. Arun Kumar, D. Shalini, B. Ishani, Y. Prem, I. S. Aidhen, Bioorg. Med. Chem. Lett. 2019, 29, 585-590. DOI: 10.1016/j.bmcl.2018.12.057

5. Synthesis of unsymmetrical linear diarylheptanoids and their enantiomers and anti proliferative activity studies, K. Sudarshan, G. Perumal, I. S. Aidhen, M. Doble Eur. J. Org. Chem. 2018, 6379-6387. DOI:10.1002/ejoc.201801211

4. Convenient synthesis of 3-glycosylated isocoumarins, K. Sudarshan, I. S. Aidhen, Eur. J. Org. Chem. 2017, 34-38. DOI: 10.1002/ejoc.201601264

3. Inhibition of the enzymes in the leukotriene and prostaglandin pathways in inflammation by 3-aryl isocoumarins, M. Ramanan, S. Sinha, K. Sudarshan, I. S. Aidhen and M. Doble, Eur. J. Med. Chem. 2016, 124, 428-434. DOI: 10.1016/j.ejmech.2016.08.066

2. Synthesis of 3-aryl isocoumarins by using acyl anion chemistry and synthesis of thunberginol A and cajanolactone A, K. Sudarshan, M. K. Manna, I. S. Aidhen, Eur. J. Org. Chem. 2015, 1797-1803. DOI: 10.1002/ejoc.201403524

1. Synthesis of (+)-centrolobine and its analogues using acyl anion chemistry, K. Sudarshan, I. S. Aidhen, Eur. J. Org. Chem. 2013, 2298-2302. DOI: 10.1002/ejoc.201300097