Structure脙脙脙脙脙脙activity relationships and sub-type selectivity in an oxabicyclic estrogen receptor 脙脙脙脙/脙脙脙脙 agonist scaffold
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摘要
An oxabicyclic template for estrogen receptor 脦脦 and 脦脦 agonists has been identified which can be tuned to provide moderate levels of selectivity for either receptor sub-type. Structure脦脦脦activity relationships within this phenol-substituted oxabicyclo[3.3.1]nonene series are described. Select compounds from the present series showed activity in vivo after oral dosing in rodent models of uterine proliferation.

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