1974
DOI: 10.1021/jm00249a021
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9,11-Seco steroids. Attempt to separate biological activities via ring cleavage

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1974
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Cited by 6 publications
(2 citation statements)
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“…Improvements in tissue selectivity have been observed with a family of D-ring halogenated estrones which have demonstrated potent lipid lowering yet diminished uterine hypertrophy relative to estrone . Other attempts to attenuate the estrogenic activity of steroids on the uterus by opening of the steroid nucleus, such as 9,11-seco steroids, have met with only limited success. , …”
Section: Estrogen Replacement Therapy For Osteoporosismentioning
confidence: 99%
See 1 more Smart Citation
“…Improvements in tissue selectivity have been observed with a family of D-ring halogenated estrones which have demonstrated potent lipid lowering yet diminished uterine hypertrophy relative to estrone . Other attempts to attenuate the estrogenic activity of steroids on the uterus by opening of the steroid nucleus, such as 9,11-seco steroids, have met with only limited success. , …”
Section: Estrogen Replacement Therapy For Osteoporosismentioning
confidence: 99%
“…105 Other attempts to attenuate the estrogenic activity of steroids on the uterus by opening of the steroid nucleus, such as 9,11-seco steroids, have met with only limited success. 106,107 A synthetic steroid with weak estrogenic, progestational, and androgenic properties that has been examined clinically is Tibolone (OD-14). 108 Tibolone has been used to treat climacteric syndome without inducing endometrial stimulation.…”
Section: Estrogen Replacement Therapy For Osteoporosismentioning
confidence: 99%