2012
DOI: 10.1016/j.bmcl.2011.11.035
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Design and synthesis of 3,5-diarylpiperidin-2,6-diones as anticonvulsant agents

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Cited by 5 publications
(3 citation statements)
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“…with significant SAR results. [56] The structural changes revealed the beneficial effect of the presence of 8-hydroxyquinol moiety for activity. These Mannich bases possesses average micromolar resistance for carcinoma cells.…”
Section: Synthesis Of "Antitumour" Moleculesmentioning
confidence: 99%
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“…with significant SAR results. [56] The structural changes revealed the beneficial effect of the presence of 8-hydroxyquinol moiety for activity. These Mannich bases possesses average micromolar resistance for carcinoma cells.…”
Section: Synthesis Of "Antitumour" Moleculesmentioning
confidence: 99%
“…al . reported a number of 8‐hydroxyquinoline‐based Mannich moieties and studied their spread inhibition with significant SAR results [56] . The structural changes revealed the beneficial effect of the presence of 8‐hydroxyquinol moiety for activity.…”
Section: Application Of Mannich Basesmentioning
confidence: 99%
“…The currently available antiepileptic drugs phenytoin, mephobarbital induce side effects such as sedation and hypnosis. 63 There is ever-mounting need for new anticonvulsant agents to control all kinds of fits, with minimal or no side effects. Recently, Obniska et al reported the synthesis and studies of Mannich bases derived from [7,8-f ]benzo-2-azaspiro[4.5]decane-1, 3-dione and [7,8-f ]benzo-1,3-diaza-spiro-decane-2,4dione 78 (scheme 25).…”
Section: Synthesis Of Anticonvulsant Moleculesmentioning
confidence: 99%