| Spiro [pyrrolidine-3, 3-oxindole] as potent anti-breast cancer compounds: Their design, synthesis, biological evaluation and cellular target identification S Hati, S Tripathy, PK Dutta, R Agarwal, R Srinivasan, A Singh, S Singh, ... Scientific reports 6 (1), 32213, 2016 | 79 | 2016 |
| Design, synthesis and evaluation of thiohydantoin derivatives as potent topoisomerase I (Top1) inhibitors with anticancer activity P Majumdar, C Bathula, SM Basu, SK Das, R Agarwal, S Hati, A Singh, ... European journal of medicinal chemistry 102, 540-551, 2015 | 74 | 2015 |
| Design, synthesis and biological evaluation of small molecules as potent glucosidase inhibitors S Hati, SM Madurkar, C Bathula, C Thulluri, R Agarwal, FA Siddiqui, ... European Journal of Medicinal Chemistry 100, 188-196, 2015 | 33 | 2015 |
| Identification of Leishmania donovani Topoisomerase 1 inhibitors via intuitive scaffold hopping and bioisosteric modification of known Top 1 inhibitors R Mamidala, P Majumdar, KK Jha, C Bathula, R Agarwal, MT Chary, ... Scientific Reports 6 (1), 26603, 2016 | 30 | 2016 |
| A novel library of -arylketones as potential inhibitors of α-glucosidase: Their design, synthesis, in vitro and in vivo studies T Luthra, R Agarwal, M Estari, U Adepally, S Sen Scientific reports 7 (1), 13246, 2017 | 28 | 2017 |
| Diverse synthesis of natural product inspired fused and spiro-heterocyclic scaffolds via ring distortion and ring construction strategies C Bathula, P Dangi, S Hati, R Agarwal, P Munshi, A Singh, S Singh, S Sen New Journal of Chemistry 39 (12), 9281-9292, 2015 | 23 | 2015 |
| CoReCG: a comprehensive database of genes associated with colon-rectal cancer R Agarwal, B Kumar, M Jayadev, D Raghav, A Singh Database 2016, baw059, 2016 | 21 | 2016 |
| Substituted furopyridinediones as novel inhibitors of α-glucosidase C Bathula, R Mamidala, C Thulluri, R Agarwal, KK Jha, P Munshi, ... RSC advances 5 (110), 90374-90385, 2015 | 14 | 2015 |
| Design, synthesis and in vitro study of densely functionalized oxindoles as potent α-glucosidase inhibitors T Luthra, KN Lalitha, R Agarwal, A Uma, S Sen Bioorganic & Medicinal Chemistry 26 (18), 4996-5005, 2018 | 13 | 2018 |
| Role of molecular docking in computer-aided drug design and development R Agarwal, A Singh, S Sen Applied Case Studies and Solutions in Molecular Docking-Based Drug Design, 1-28, 2016 | 6 | 2016 |
| Calcium-induced conformational changes of Thrombospondin-1 signature domain: implications for vascular disease A Gupta, R Agarwal, A Singh, S Bhatnagar Journal of Receptors and Signal Transduction 37 (3), 239-251, 2017 | 2 | 2017 |
| Corrigendum to ‘Design, synthesis and in vitro study of densely functionalized oxindoles as potent α-glucosidase inhibitors’[Bioorg. Med. Chem. 26 (18)(2018) 4996–5005] T Luthra, KN Lalitha, R Agarwal, A Uma, S Sen Bioorganic & Medicinal Chemistry 26 (23-24), 6153-6153, 2018 | | 2018 |
