![Leuprolide acetate furazone [2H]C1([2H])N(C(C2C=CC=CC=2)C2C=CC(Cl)=CC=2)C([2H])([2H])C([2H])([2H])N(CCOCC(O)=O)C1([2H])[2H]](https://cdn.shopify.com/s/files/1/0389/1897/9723/products/M9797_1621560814.gif?v=1621560816)
Leuprolide acetate furazone [2H]C1([2H])N(C(C2C=CC=CC=2)C2C=CC(Cl)=CC=2)C([2H])([2H])C([2H])([2H])N(CCOCC(O)=O)C1([2H])[2H]
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Leuprolide acetate furazone [2H]C1([2H])N(C(C2C=CC=CC=2)C2C=CC(Cl)=CC=2)C([2H])([2H])C([2H])([2H])N(CCOCC(O)=O)C1([2H])[2H]Leuprolide acetate is the acetate salt of a synthetic nonapeptide analogue of gonadotropin releasing hormone. Leuprolide binds to and activates gonadotropin releasing hormone (GnRH) receptors. Continuous, prolonged administration of leuprolide in males results in pituitary GnRH receptor desensitization and inhibition of pituitary secretion of follicle stimulating hormone (FSH) and luteinizing hormone (LH), leading to a significant decline in
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