
Journal of Medicinal Chemistry p. 2464 - 2468 (1991)
Update date:2022-08-03
Topics:
Nickisch
Beier
Bittler
Elger
Laurent
Losert
Nishino
Schillinger
Wiechert
Several steroidal 6,6-ethylene-15,16-methylene 17-spirolactones were synthesized to find new progestogens that exhibit both progestational and antimineralocorticoidal activities. The influence of substituents in the 10- and 13-position of the steroidal framework on both properties was investigated. It was found that only compound 12, carrying methyl groups at the 10- and 13-positions, possesses high progestational and antimineralocorticoidal activity.
View MoreContact:+86-570-4336358
Address:No.87 Building,Tianqian,Sidu Town
Contact:86-310-8067016
Address:East Fuhua Road,Tiexi Chemical Industrial Estate,Hebei,China
Hangzhou jls Flame Retardants Chemical Co.,Ltd
Contact:+86-571-87250387/87250386
Address:MOGANSHAN RODA 1418# SHANGCHENG INDUSTRIAL PARK
Laohekou Jinghong Chemical Co.,Ltd
Contact:+86-0710-3702747
Address:163.East,Huagong Road,Laohekou
Shanghai ZaiQi Bio-Tech Co., Ltd.,
Contact:+86-21-5482 4098
Address:Bldg. No.7, No.201 MinYi Rd,Songjiang CaoHeJing High-Tech Park Shanghai 201516 P,R,China
Doi:10.1021/jo00362a005
(1986)Doi:10.1021/ol8002749
(2008)Doi:10.1039/jr9560004411
(1956)Doi:10.1016/j.tet.2008.01.034
(2008)Doi:10.1002/anie.200800066
(2008)Doi:10.1080/15257770701257236
(2007)