| Fused heterocyclic compounds as potent indoleamine-2, 3-dioxygenase 1 inhibitors S Panda, A Roy, SJ Deka, V Trivedi, D Manna ACS Medicinal Chemistry Letters 7 (12), 1167-1172, 2016 | 48 | 2016 |
| Transition metal, azide, and oxidant-free homo-and heterocoupling of ambiphilic tosylhydrazones to the regioselective triazoles and pyrazoles S Panda, P Maity, D Manna Organic letters 19 (7), 1534-1537, 2017 | 43 | 2017 |
| Nitrobenzofurazan derivatives of N′-hydroxyamidines as potent inhibitors of indoleamine-2, 3-dioxygenase 1 S Paul, A Roy, SJ Deka, S Panda, V Trivedi, D Manna European Journal of Medicinal Chemistry 121, 364-375, 2016 | 34 | 2016 |
| Diphenylethylenediamine-based potent anionophores: transmembrane chloride ion transport and apoptosis inducing activities N Akhtar, A Saha, V Kumar, N Pradhan, S Panda, S Morla, S Kumar, ... ACS applied materials & interfaces 10 (40), 33803-33813, 2018 | 31 | 2018 |
| 4, 5-Disubstituted 1, 2, 3-triazoles: effective inhibition of indoleamine 2, 3-dioxygenase 1 enzyme regulates T cell activity and mitigates tumor growth S Panda, N Pradhan, S Chatterjee, S Morla, A Saha, A Roy, S Kumar, ... Scientific Reports 9 (1), 18455, 2019 | 27 | 2019 |
| Phosphate bioisostere containing amphiphiles: a novel class of squaramide-based lipids A Saha, S Panda, S Paul, D Manna Chemical communications 52 (60), 9438-9441, 2016 | 23 | 2016 |
| Mild method for the synthesis of 1H-indazoles through oxime-phosphonium ion intermediate S Paul, S Panda, D Manna Tetrahedron letters 55 (15), 2480-2483, 2014 | 22 | 2014 |
| Synthesis and evaluation of oxindoles as promising inhibitors of the immunosuppressive enzyme indoleamine 2, 3-dioxygenase 1 S Paul, A Roy, SJ Deka, S Panda, GN Srivastava, V Trivedi, D Manna Medchemcomm 8 (8), 1640-1654, 2017 | 17 | 2017 |
| Ring-Opening of Indoles: An Unconventional Route for the Transformation of Indoles to 1H-Pyrazoles Using Lewis Acid S Panda, N Pradhan, D Manna ACS Combinatorial Science 20 (10), 573-578, 2018 | 15 | 2018 |
| Membrane interaction and protein kinase C-C1 domain binding properties of 4-hydroxy-3-(hydroxymethyl) phenyl ester analogues D Talukdar, S Panda, R Borah, D Manna The Journal of Physical Chemistry B 118 (27), 7541-7553, 2014 | 15 | 2014 |
| Azidophosphonate Chemistry as a Route for a Novel Class of Vesicle‐Forming Phosphonolipids A Saha, S Panda, N Pradhan, K Kalita, V Trivedi, D Manna Chemistry–A European Journal 24 (5), 1121-1127, 2018 | 11 | 2018 |
| Synthesis and protein kinase C (PKC)-C1 domain binding properties of diacyltetrol based anionic lipids N Mamidi, S Panda, R Borah, D Manna Molecular Biosystems 10 (11), 3002-3013, 2014 | 7 | 2014 |
| Innovative Strategies for the Construction of Diverse 1′-Modified C-Nucleoside Derivatives S Panda, TN Poudel, P Hegde, CC Aldrich The Journal of Organic Chemistry 86 (23), 16625-16640, 2021 | 6 | 2021 |
| 1′-Cyano intermediate enables rapid and stereoretentive access to 1′-modified Remdesivir nucleosides TN Poudel, S Panda, M Orimoloye, P Hegde, CC Aldrich The Journal of Organic Chemistry 87 (21), 14452-14462, 2022 | 1 | 2022 |
| Elucidating the interaction of γ-hydroxymethyl-γ-butyrolactone substituents with model membranes and protein kinase C–C1 domains R Borah, N Mamidi, S Panda, S Gorai, SK Pathak, D Manna Molecular BioSystems 11 (5), 1389-1399, 2015 | 1 | 2015 |
| Drugging the microbiome: targeting small microbiome molecules S Sharma, P Hegde, S Panda, MO Orimoloye, CC Aldrich Current Opinion in Microbiology 71, 102234, 2023 | | 2023 |
| Next generation remdesivir antivirals CC Aldrich, S Panda, T Poudel US Patent App. 17/579,271, 2022 | | 2022 |
| Synthesis of n heterocycles as potential inhibitors of the immunosuppressive enzyme indoleamine 2 3 dioxygenase 1 S Panda Guwahati, 2018 | | 2018 |
Dr. Debasis MannaIndian Institute of Technology GuwahatiVerified email at iitg.ac.in
