Seshagiri Rao Casturi
Dr. Reddy's Laboratories (India)(IN)
Publications by Year
Research Areas
Inflammatory mediators and NSAID effects, Synthesis and biological activity, Synthesis of β-Lactam Compounds, Synthesis and Reactions of Organic Compounds, Estrogen and related hormone effects
Most-Cited Works
- → 3-O-Substituted benzyl pyridazinone derivatives as COX inhibitors(2002)60 cited
- → Conformationally restricted 3,4-diarylfuranones (2,3a,4,5-tetrahydronaphthofuranones) as selective cyclooxygenase-2 inhibitors(2003)48 cited
- → Synthesis and Cyclooxygenase-2 Inhibiting Property of 1,5-Diarylpyrazoles with Substituted Benzenesulfonamide Moiety as Pharmacophore: Preparation of Sodium Salt for Injectable Formulation†(2003)43 cited
- → Evaluation of glycolamide esters of indomethacin as potential cyclooxygenase-2 (COX-2) inhibitors(2006)41 cited
- → 1,2-Diaryl-1-ethanone and pyrazolo [4,3-c] quinoline-4-one as novel selective cyclooxygenase-2 inhibitors(2003)39 cited
- → Methanesulfonamide group at position-4 of the C-5-phenyl ring of 1,5-diarylpyrazole affords a potent class of cyclooxygenase-2 (COX-2) inhibitors(2004)31 cited
- → N-Acylated sulfonamide sodium salt: A prodrug of choice for the bifunctional 2-hydroxymethyl-4-(5-phenyl-3-trifluoromethyl-pyrazol-1-yl) benzenesulfonamide class of COX-2 inhibitors(2006)14 cited
- → 2-Hydroxymethyl-4-[5-(4-methoxyphenyl)-3-trifluoromethyl-1H-1-pyrazolyl]-1-benzenesulfonamide (DRF-4367): an orally active COX-2 inhibitor identified through pharmacophoric modulation(2004)13 cited
- → Synthesis and Cyclooxygenase-2 (COX-2) Inhibiting Properties of 1,5- Diarylpyrazoles Possessing N-Substitution on the Sulfonamide (-SO2NH2) Moiety †(2005)9 cited
- → Development of COX-2 Selective Inhibitors - Therapeutic Perspectives(2005)4 cited