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  2. Aromatase inhibitor - Wikipedia

    en.wikipedia.org/wiki/Aromatase_inhibitor

    Ovarian stimulation with the aromatase inhibitor letrozole has been proposed for ovulation induction in order to treat unexplained female infertility. In a multi-center study funded by the National Institute of Child Health and Development, ovarian stimulation with letrozole resulted in a significantly lower frequency of multiple gestation (i.e., twins or triplets) but also a lower frequency ...

  3. Female fertility agents - Wikipedia

    en.wikipedia.org/wiki/Female_fertility_agents

    Among all aromatase inhibitors, Letrozole is commonly used for improving female fertility. It works by inhibiting aromatase which is an enzyme that catalyses the conversion of androstenedione and testosterone to estrogen by hydroxylation. Hence, Letrozole inhibits the synthesis of estrogen. [18]

  4. Fertility medication - Wikipedia

    en.wikipedia.org/wiki/Fertility_medication

    Although primarily used in breast cancer treatment, aromatase inhibitors (particularly generic letrozole) are also used in ovulation induction. Aromatase inhibitors are a common fertility treatment to treat women with PCOS.

  5. 1,4,6-Androstatriene-3,17-dione - Wikipedia

    en.wikipedia.org/wiki/1,4,6-Androstatriene-3,17...

    1,4,6-Androstatriene-3,17-dione (ATD) is a potent irreversible aromatase inhibitor that inhibits estrogen biosynthesis by permanently binding and inactivating aromatase in adipose and peripheral tissue. [1] It is used to control estrogen synthesis. [2]

  6. Letrozole - Wikipedia

    en.wikipedia.org/wiki/Letrozole

    Letrozole is an orally active, nonsteroidal, selective aromatase inhibitor and hence an antiestrogen. It prevents aromatase from producing estrogens by competitive, reversible binding to the heme of its cytochrome P450 unit. The action is specific, and letrozole does not reduce production of corticosteroids. [citation needed

  7. 4-Androstene-3,6,17-trione - Wikipedia

    en.wikipedia.org/wiki/4-Androstene-3,6,17-trione

    4-AT is a potent irreversible aromatase inhibitor that inhibits estrogen biosynthesis by permanently binding and inactivating aromatase in adipose and peripheral tissue. [4] [5] [6] Aromatase is responsible for the conversion of testosterone to estradiol.