Literature DB >> 1394662

Agents for the treatment of overactive detrusor. III. Synthesis and structure-activity relationships of N-(4-amino-2-butynyl)acetamide derivatives.

K Take1, K Okumura, K Tsubaki, T Terai, Y Shiokawa.   

Abstract

A series of N-(4-amino-2-butynyl)acetamides were synthesized and examined for their inhibitory activity on detrusor contraction and mydriatic activity as an index of anticholinergic side effect. Among those compounds synthesized, (+)-2-cyclohexyl-N-(4-dimethylamino-2-butynyl)-2-hydroxy-2-phenylacet amide hydrochloride ((+)-13b.HCl), 2-cyclohexyl-2-hydroxy-N-(4-methylamino-2-butynyl)-2-phenylacetamide+ ++ hydrochloride (13c.HCl), N-(4-dimethylamino-2-butynyl)-2,2-diphenyl-2-hydroxyacetamide hydrochloride (14a.HCl), and 2,2-diphenyl-N-(4-ethylamino-2-butynyl)-2-hydroxyacetamide hydrochloride (14b.HCl) showed equipotent inhibitory activity on detrusor contraction to oxybutynin (1) and less mydriatic activity. Further evaluation of these compounds as an agent for the treatment of overactive detrusor has been examined.

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Year:  1992        PMID: 1394662     DOI: 10.1248/cpb.40.1415

Source DB:  PubMed          Journal:  Chem Pharm Bull (Tokyo)        ISSN: 0009-2363            Impact factor:   1.645


  1 in total

1.  Novel Potent Muscarinic Receptor Antagonists: Investigation on the Nature of Lipophilic Substituents in the 5- and/or 6-Positions of the 1,4-Dioxane Nucleus.

Authors:  Fabio Del Bello; Alessandro Bonifazi; Gianfabio Giorgioni; Alessandro Piergentili; Maria Giovanna Sabbieti; Dimitrios Agas; Marzia Dell'Aera; Rosanna Matucci; Marcin Górecki; Gennaro Pescitelli; Giulio Vistoli; Wilma Quaglia
Journal:  J Med Chem       Date:  2020-05-19       Impact factor: 7.446

  1 in total

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