Leuprorelin Acetate
Leuprorelin Acetate (Leupron) is a synthetic nonapeptide analogue of LHRH, used for the treatment of advanced prostate cancer. As an LH-RH antagonist, it initially stimulates then suppresses gonadotropin secretion, reducing testosterone to castration levels.

Description
Product Introduction
Leuprolide acetate is a commonly used hormone anti-cancer drug, it is an acetate of leuprolide which is a nonapeptide synthetic analogue of LHRH (one kind decapeptide), it is a LH-RH antagonist. LHRH is produced by the hypothalamus, it can promote pituitary for the release of gonadotropins and follicle-stimulating hormone (FSH) and luteinizing hormone (LH). This product's structure is similar to LHRH, its acting on the anterior pituitary which prompts FSH, LH release function, increases serum concentrations of testosterone and dihydrotestosterone.
But in about one week after use of the product, the number of active receptors will be reduced, and gonadotropin secretion will be reduced. After 2 to 4 weeks, the concentration of testosterone and dihydrotestosterone can be reduced to castration levels. After the withdrawal, gonadotropin and androgen concentrations can be recovered to normal.
Application
Leuprolide acetate (Leupron) is used to treat Prostatic carcinoma. It has also been investigated for the treatment of advanced breast cancer.
Product Description
- Application Field
- Prostate cancer, breast cancer, gynecological diseases, precocious puberty, peptide drug API
- Packaging
- Custom packaging per client requirements
- Storage Conditions
- -20°C, protected from light, sealed storage
- Shelf Life
- 2 years
Specifications
| Appearance | White to off-white powder |
| Purity (HPLC) | ≥98% |




