4-[(1, 2-Dihydro-2-oxo-3H-indol-3-ylidene) amino]-N-(4, 6-dimethyl-2-pyrimidinyl)-
benzenesulphonamide (SPIII-5H) and related compounds were tested for antiviral activity …

The article describes the design, synthesis, and characterization of a new series of 8‐
trifluoromethylquinoline substituted pyrazole‐3‐carboxamides (9a, 9b, 9c, 9d, 9e, 9f, 9g, 9h …

The hydrazide obtained from furan‐2 (3 H)‐one integrated with a quinolin‐2 (1 H)‐one core
reported previously by our research group was utilized as a building block synthon to obtain …

In this study, we reported the synthesis and biological characterization of a novel series of
furan-carboxamide derivatives that were potent inhibitors of the influenza A H5N1 virus. The …

The 3-(2-adamantyl) pyrrolidines 8a–g, 14 were synthesized and evaluated for activity
against influenza A virus. The parent N–H compound 14 was several times more active than …

A series of camphor derived imines was synthesised and evaluated in vitro for antiviral
activity. Theoretical evaluations of ADME properties were also carried out. Most of these …

Novel antiherpetic 3-quinolinecarboxamides were discovered as part of a drug discovery
program at Sterling Winthrop Inc. A major goal of this research was to identify novel non …

Synthesis of 3,6,7-substituted-quinoxalin-2-ones for evaluation of antimicrobial and
anticancer activity. Part 2 - ScienceDirect Skip to main contentSkip to article Elsevier logo …

This report focuses on the synthesis of 2-phenyl-7-substitutedquinoline-4-carboxylic acid
derivatives through both conventional and microwave-irradiated methods. Intermediate 7 …

Evidences of oseltamivir resistant influenza patients raised the need of novel neuraminidase
inhibitors. In this study, five oseltamivir analogs PMC-31–PMC-36, synthesised according to …