Author/Authors :
Yoshitake Kanbe، نويسنده , , Myung-Hwa Kim، نويسنده , , Masahiro Nishimoto، نويسنده , , Yoshihito Ohtake، نويسنده , , Toshiaki Tsunenari، نويسنده , , Kenji Taniguchi and Kenichi Nakashi ، نويسنده , , Iwao Ohizumi، نويسنده , , Shin-ichi Kaiho، نويسنده , , Yoshiaki Nabuchi، نويسنده , , Setsu Kawata، نويسنده , , Kazumi Morikawa، نويسنده , , Jae-Chon Jo، نويسنده , , Hee-An Kwon، نويسنده , , Hyun-Suk Lim، نويسنده , , Hak-Yeop Kim، نويسنده ,
Abstract :
In order to search for alternatives to the sulfoxide moiety in the long side chain of pure antiestrogens, several molecules that may interact with water in a fashion similar to ICI164,384 were designed and it was found that compounds with the carboxy, the sulfamide, or the sulfonamide instead of the sulfoxide moiety also functioned as pure antiestrogens. Interestingly, the compound possessing the carboxy moiety showed superior antiestrogen activity compared to ICI182,780 when dosed orally. Results of the pharmacokinetic evaluation indicated that the potent antiestrogen activity at oral dosing attributed to both the improved absorption from the intestinal wall and the metabolic stability of the compound in liver.
Keywords :
Thiochroman , Pure antiestrogen , Chroman , estrogen receptor