Structure-Activity Relationships and Design of Focused Libraries Tailored for Staphylococcus Aureus Inhibition. [PDF]
Marbán-González A, Medina-Franco JL.
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Bench-stable azidodifluoromethyl imidazolium reagents unlock the synthetic potential of carbonimidic difluorides. [PDF]
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Design, synthesis, and antitumor evaluation of new functionalized spiroindenopyridotriazinepyrans. [PDF]
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Untargeted metabolomics reveals key metabolic alterations in pediatric epilepsy with insights into Tryptophan metabolism and the gut-brain axis. [PDF]
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Anti-Parkinsonian 4-hydroxy-2-pyridones from an endolichenic fungus, Tolypocladium sp. (strain CNC14). [PDF]
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Tetrachlorobis(2-pyridone)-bis(μ2-2-pyridone)-dicopper
Acta Crystallographica Section C Crystal Structure Communications, 1993In this structure two Cu II centres 3.4448 (11) A apart are bridged asymmetrically by two 2-pyridone ligands and each is further coordinated by three terminal ligands (two chlorides and one 2-pyridone). Each molecule has an approximate, non-crystallographic centre of symmetry.
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Pyridones as Potential Antitumor Agents II: 4-Pyridones and Bioisosteres of 3-Acetoxy-2-pyridone
Journal of Pharmaceutical Sciences, 1980Pyridone structural requirements for activity against murine P-388 leukemia have been extended to isosteric analogs of 3-hydroxy-4-pyridone, a compound previously found to have activity. An amino group can be substituted for the 3-hydroxyl function with retention of activity.
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