Sankar K. Guchhait
Affiliations: | 2007- | National Institute of Pharmaceutical Education and Research, Mohali |
Area:
Synthetic organic chemistry, natural products chemistry, medicinal chemistry, anticancer drugsWebsite:
https://www.skguchhait.com/homeGoogle:
"Sankar K. Guchhait"Bio:
(born 1973)
Mean distance: (not calculated yet)
Parents
Sign in to add mentor| Brindaban Chandra Ranu | grad student | 1996-2001 | Indian Association for the Cultivation of Science |
| George W. Kabalka | post-doc | 2002-2004 | University of Tennessee, Knoxville |
| Gabriel Fenteany | post-doc | 2004-2005 | University of Illinois, Chicago |
| Michael C. Pirrung | post-doc | 2005-2006 | UC Riverside |
Children
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Publications
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| Saini M, Paul S, Acharya A, et al. (2024) Scaffold overlay of flavonoid-inspired molecules: Discovery of 2,3-diaryl-pyridopyrimidin-4-imine/ones as dual hTopo-II and tubulin targeting anticancer agents. Bioorganic Chemistry. 152: 107738 |
| Yadav M, Roy N, Mandal K, et al. (2024) Rutaecarpine-inspired scaffold-hopping strategy and Ullmann cross-coupling based synthetic approach: Identification of pyridopyrimidinone-indole based novel anticancer chemotypes. Bioorganic & Medicinal Chemistry. 109: 117799 |
| Krishna Rao V, Paul S, Gulkis M, et al. (2024) Molecular editing of enabling discovery of benzodithiazinedioxide-guanidines as anticancer agents. Rsc Medicinal Chemistry. 15: 937-962 |
| Acharya A, Yadav M, Nagpure M, et al. (2023) Molecular medicinal insights into scaffold hopping-based drug discovery success. Drug Discovery Today. 103845 |
| Rao VK, Ashtam A, Panda D, et al. (2023) Natural product-inspired discovery of trimethoxyphenyl-1,2,4-triazolo-sulfonamides as potent tubulin polymerization inhibitors. Chemmedchem. e202300562 |
| Giri P, Batra PJ, Kumari A, et al. (2023) Development of QTMP: A promising anticancer agent through NP-Privileged Motif-Driven structural modulation. Bioorganic & Medicinal Chemistry. 95: 117489 |
| Sisodiya S, Acharya A, Nagpure M, et al. (2022) A cascade reaction of indolyl-migratory isocyanide insertion, scaffold rearrangement and redox-neutral event with isocyanide as a CH-N synthon efficiently constructs indolylisoindolinones. Chemical Communications (Cambridge, England). 58: 11827-11830 |
| Shah AP, Hura N, Babu NK, et al. (2022) A "Core-Linker-Polyamine (CLP)" strategy enabling rapid discovery of antileishmanial aminoalkyl-quinoline-carboxamides that target oxidative stress mechanism. Chemmedchem |
| Kumar G, Das C, Acharya A, et al. (2022) Organocatalyzed umpolung addition for synthesis of heterocyclic-fused arylidene-imidazolones as anticancer agents. Bioorganic & Medicinal Chemistry. 67: 116835 |
| Kumari A, Jaiswal T, Kumar V, et al. (2022) Identification of 2-arylquinazolines with alkyl-polyamine motifs as potent antileishmanial agents: synthesis and biological evaluation studies. Rsc Medicinal Chemistry. 13: 320-326 |