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Quingestanol is a synthetic progestogen primarily investigated for its contraceptive properties. It functions by activating estrone sulfatase and binding to progesterone receptors. Its contraceptive mechanism involves the inhibition of gonadotropins, leading to altered ovulation and disturbed corpus luteum function. Additionally, it modifies cervical mucus properties, inhibiting sperm penetration, and induces histological, histochemical, and ultrastructural changes in the endometrium. It has been studied as an oral contraceptive, both as a microdose monotherapy and in combination with estrogens.
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