| Literature DB >> 1151995 |
H Y Aboul-Enein, C W Schauberger, A R Hansen, L J Fischer.
Abstract
Two synthetic pathways are described for the preparation of 4-hydroxy-2-ethyl-2-phenylglutarimide (2), an active hydroxylated metabolite of glutethimide (1). Fourteen other glutethimide analogs were also synthesized and tested for biological activity. Most of the analogs exhibited sedative-hypnotic properties and compound 2 possessed the greatest activity compared to the parent drug. 4-Amino-2-ethyl-2-phenylglutarimide and 4-hydroxy-2-ethyl-2-phenylglutaconimide (13) exhibited the greatest potential as anticonvulsant agents. The structure-activity relationships of the series are discussed.Entities:
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Year: 1975 PMID: 1151995 DOI: 10.1021/jm00241a019
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446