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        | puried from postmenopausal women, mixture of FSH and LH |  | 
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        | purified human follicle stimulating hormone |  | 
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        | SHBG, alpha and beta receptors. Bind to EREs |  | 
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        | progesterone; bind to nuclear receptors (transcription factors) and regular gene expression; carbohydrate metabolism |  | 
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        | progesterone; bind to nuclear receptors (transcription factors) and regular gene expression; carbohydrate metabolism |  | 
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        | progesterone; bind to nuclear receptors (transcription factors) and regular gene expression; carbohydrate metabolism |  | 
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        | progesterone; bind to nuclear receptors (transcription factors) and regular gene expression; carbohydrate metabolism |  | 
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        | progesterone; bind to nuclear receptors (transcription factors) and regular gene expression; carbohydrate metabolism |  | 
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        | progesterone; bind to nuclear receptors (transcription factors) and regular gene expression; carbohydrate metabolism |  | 
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        | progesterone; bind to nuclear receptors (transcription factors) and regular gene expression; carbohydrate metabolism |  | 
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        | progesterone; bind to nuclear receptors (transcription factors) and regular gene expression; carbohydrate metabolism |  | 
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        | SERM; similar to Tamoxifen |  | 
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        | SERM; inhibits estrogen neg. feedback inhibition of FSH and LH release; may exhibit anti estrogen effects on uterus and cervix |  | 
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        | estrogen antagonist; treatment of breast cancer |  | 
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        | aromatase inhibitors (AI); used in adjunct treatment in ER positive breast cancer |  | 
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        | aromatase inhibitors (AI); used in adjunct treatment in ER positive breast cancer |  | 
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        | aromatase inhibitors (AI); used in adjunct treatment in ER positive breast cancer |  | 
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        | anti-progesterone; inhibits progesterone; early termination of pregnancy |  | 
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        | inhbits FSH and LH; used for endometriosis, and fibrocyctic breast disease |  | 
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        | androgen; anabolic agent that is converted via 5- alpha rectase |  | 
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        | androgen replacement therapy |  | 
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        | anabolic steroid for anemia, bone pain in osteoporsis, and increasing weight (androgen receptor agonits) |  | 
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        | anabolic steroid for anemia, bone pain in osteoporsis, and increasing weight (androgen receptor agonits) |  | 
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        | anabolic steroid for anemia, bone pain in osteoporsis, and increasing weight (androgen receptor agonits) |  | 
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        | anabolic steroid for anemia, bone pain in osteoporsis, and increasing weight (androgen receptor agonits) |  | 
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        | antifungal; inhibit steroid synthesis (anti-androgen) |  | 
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        | 5-alpha reductase inhibitor; male pattern baldness; type II |  | 
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        | 5-alpha reductase inhibitor; equal for type I and II |  | 
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        | androgen receptor blocker; blockers androgen receptors in prostate to reduce growth and treat metastatic prostate cancer |  | 
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        | androgen receptor blocker; blockers androgen receptors in prostate to reduce growth and treat metastatic prostate cancer |  | 
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        | androgen receptor blocker; blockers androgen receptors in prostate to reduce growth and treat metastatic prostate cancer |  | 
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        | steroid androgen receptor antagonist |  | 
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        | alkylating agent; widest spectrum of nitrogen mustards; activated by CYP450 to active metbolite--bladder toxcity |  | 
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        | antracycline antiobiotics; inhibits topoisomerase leading to DNA beaks and release of free radicals |  | 
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        | antracycline antiobiotics; inhibits topoisomerase leading to DNA beaks and release of free radicals |  | 
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        | antracycline antiobiotics; inhibits topoisomerase leading to DNA beaks and release of free radicals |  | 
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        | antracycline antiobiotics; inhibits topoisomerase leading to DNA beaks and release of free radicals |  | 
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        | antedote for anthracycline toxicity |  | 
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        | antidote for anthracycline induced cardiomyopathy; iron chelator |  | 
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