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Generated: December 15, 2017

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Title: Tri-phenyl alkane derivatives and their oestrogenic, anti-oestrogenic and progestanic uses
Abstract:
Inventor(s): Toivola; Reijo J. (Oulu, FI), Karjalainen; Arto J. (Oulu, FI), Kurkela; Kauko O. A. (Oulu, FI), Soderwall; Marja-Liisa (Oulu, FI), Kangas; Lauri V. M. (Turku, FI), Blanco; Guillermo L. (Oulu, FI), Sundquist; Hannu K. (Kaarina, FI)
Assignee: Farmos Group Ltd. (Turku, FI)
Filing Date:Oct 12, 1989
Application Number:07/420,437
Claims:1. A compound of the formula: ##STR51## where n is 0 to 4, R.sub.1, and R.sub.2, which can be the same or different, are H or OH, R.sub.3 is --O--(CH.sub.2).sub.m --CH.sub.2 --NR.sub.6 R.sub.7 in which m is 1 to 2, R.sub.6 and R.sub.7, which can be the same or different, are H or an alkyl group of 1 to 4 carbon atoms or --NR.sub.6 R.sub.7 can form a pyrrolidinyl group and R.sub.4 is halogen, or a non-toxic, pharmaceutically acceptable salt or N-oxide thereof.

2. A compound according to claim 1 in which R.sub.6 is CH.sub.3 or C.sub.2 H.sub.5 ; R.sub.7 is H, CH.sub.3 or C.sub.2 H.sub.5, or NR.sub.6 R.sub.7 together form a pyrrolidinyl group.

3. A compound according to claim 1 which is 4-chloro-1,2-diphenyl-1-[4-[2-(1-pyrrolidinyl)ethoxy]phenyl]-butane, (RR,SS), or a non-toxic pharmaceutically acceptable salt.

4. A compound according to claim 1 which is 4-chloro-1,2-diphenyl-1-[4-[2-(1-pyrrolidinyl)ethoxy]phenyl]-butane, (RS,SR), or a non-toxic pharmaceutically acceptable salt.

5. A pharmaceutical composition comprising an amount effective to product an oestrogenic, anti-oestrogenic or progestanic effect, of a compound according to claim 1 or a non-toxic pharmaceutically acceptable salt thereof, and a compatible pharmaceutically acceptable carrier therefor.

6. A method of producing an oestrogenic, anti-oestrogenic or progestanic effect in a subject in which such an effect is desired which comprises administering to said subject a compound according to claim 1 or a non-toxic pharmaceutically acceptable salt thereof, in an amount sufficient to produce the desired effect.

7. A method according to claim 6 in which an antioestrogenic effect is produced in a subject suffering from an oestrogen-dependent tumor.
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