Nafarelin Acetate

Nafarelin Acetate is the acetate salt form of nafarelin, a modified synthetic porcine luteinizing hormone (LH)-releasing hormone peptide analog, with gonadotropin-releasing hormone (GnRH) agonist activity. Upon nasal inhalation, nafarelin acetate binds to the GnRH receptor. This initially results in the release of the gonadotropins, follicle-stimulating hormone (FSH) and LH, from the pituitary gland; however, prolonged stimulation of the GnRH receptor desensitizes the receptor, which leads to decreased secretion of FSH and LH. In females, the inhibition of gonadotropin secretion causes hypogonadotropic hypogonadism leading to decreased production of estrogen and progesterone and anovulation. In males, the inhibition of LH secretion prevents the production and release of testosterone from Leydig cells in the testes and causes a significant decline in testosterone production that is near the levels seen following castration.|A potent synthetic agonist of GONADOTROPIN-RELEASING HORMONE with 3-(2-naphthyl)-D-alanine substitution at residue 6. Nafarelin has been used in the treatments of central PRECOCIOUS PUBERTY and ENDOMETRIOSIS.

Molecular Weight:1400.5
Hydrogen Bond Donor Count:18
Hydrogen Bond Acceptor Count:18
Rotatable Bond Count:33
Exact Mass:1399.66731982
Monoisotopic Mass:1399.66731982
Topological Polar Surface Area:513
Heavy Atom Count:101
Complexity:2760
Defined Atom Stereocenter Count:9
Covalently-Bonded Unit Count:3
Compound Is Canonicalized:Yes