Compounds having the structure of formula I are provided. In formula I,
R.sub.1 is H, OH, substituted or unsubstituted C.sub.1 to C.sub.3 alkyl,
C.sub.1 to C.sub.3 perfluoroalkyl, or COR.sub.6; R.sub.6 is H,
substituted or unsubstituted C.sub.1 to C.sub.4 alkyl, aryl, substituted
or unsubstituted C.sub.1 to C.sub.4 alkoxy, substituted or unsubstituted
C.sub.1 to C.sub.3 aminoalkyl; R.sub.2 and R.sub.3 are H, substituted or
unsubstituted C.sub.1 to C.sub.6 alkyl, C.sub.1 to C.sub.6
perfluoroalkyl, substituted or unsubstituted C.sub.2 to C.sub.6 alkenyl,
substituted or unsubstituted C.sub.2 to C.sub.6 alkynyl, substituted or
unsubstituted C.sub.3 to C.sub.6 cycloalkyl, substituted or unsubstituted
aryl, or substituted or unsubstituted heterocyclic; or R.sub.2 and
R.sub.3 are fused to form spirocyclic rings; R.sub.4 is NHR.sub.7,
OR.sub.7, NHSO.sub.2R.sub.7, or OSO.sub.2R.sub.7; Q is O, S, NR.sub.8, or
CR.sub.9R.sub.10; or a pharmaceutically acceptable salt, ester, or
prodrug thereof. Such compounds are useful as progesterone receptor
modulators and for treating progesterone receptor related conditions.
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