Chemical and Pharmaceutical Bulletin p. 507 - 515 (1993)
Update date:2022-08-04
Topics:
Take
Okumura
Tsubaki
Terai
Shiokawa
A series of pyrrolidine derivatives were synthesized and examined for inhibitory activity on detrusor contraction in vivo. Among those compounds, 5,5-dimethyl-2-(2,2-diphenylethyl)-3-isopropylidenepyrrolidine hydrochloride (41 · HCl), 2-(2,2-di(4-fluorophenyl)ethylene)-5,5-dimethyl-3-isopropylidenepyrrol idine hydrochloride (42 · HCl), (+)5,5-dimethyl-2-(N,N-diphenylaminomethyl)-3-isopropylidenepyrrolidin e hydrochloride (+)-(43a · HCl),(-)-5,5-dimethyl-2-(N,N-diphenylaminomethyl)-3-isopropylidenepyrr olidine hydrochloride (-)-(43a · HCl), and 2-(N,N-di(4-fluorophenyl)aminomethyl)-5,5-dimethyl-3-isopropylidenepyr rolidine methanesulfonate (43b · MsOH) showed stronger inhibitory activity on detrusor contraction than terodiline.
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Doi:10.1134/S1070363213100174
(2013)Doi:10.1016/S0040-4039(01)92391-3
(1981)Doi:10.1021/jm9800907
(1998)Doi:10.1016/0014-3057(79)90203-9
(1979)Doi:10.1021/ja410686v
(2013)Doi:10.1016/0022-328X(93)83170-Z
(1993)
