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Leuprorelin

  Cat. No.:  DC22504   Featured
Chemical Structure
53714-56-0
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More than 5000 active chemicals with high quality for research!
Field of application
Leuprorelin (Leuprolide) is a GnRH analog and agonist of GnRH receptor, interrupts the normal pulsatile stimulation and desensitizing of the GnRH receptors..
Cas No.: 53714-56-0
Chemical Name: Leuprolide acetate
Synonyms: Leuprorelin;5-OXOPRO-HIS-TRP-SER-TYR-D-LEU-LEU-ARG-PRO-NHC2H5;[DES-GLY10, DLEU6, PRO9]-LH-RH, ETHYL AMIDE;[DES-GLY10, DLEU6, PRO9]-LUTEINIZING HORMONE-RELEASING HORMONE, ETHYL AMIDE;[DES-GLY10, DLEU 6, PRONHET9];(DES-GLY10,D-LEU6,PRO-NHET9)-GONADOTROPIN-RELEASING HORMONE;(DES-GLY10,D-LEU6,PRO-NHET9)-LHRH;[DES-GLY10, D-LEU6, PRO-NHET9]-LH-RH (HUMAN);(DES-GLY10,D-LEU6,PRO-NHET9)-LUTEINIZING HORMONE-RELEASING FACTOR;(DES-GLY10,D-LEU6,PRO-NHET9)-LUTEINIZING HORMONE-RELEASING HORMONE;[DES-GLY10, D-LEU6, PRO-NHET9]-LUTEINIZING HORMONE-RELEASING HORMONE HUMAN;DES-GLY10,[P-LEU6]-LH-RH ETHYLAMIDE;GLP-HIS-TRP-SER-TYR-D-LEU-LEU-ARG-PRO-NHET;LEUPROLIDE ACETATE;LEUPROLIDE (HUMAN);LEUPRORELIN ACETATE;LH-RH LEUPROLIDE;PGLU-HIS-TRP-SER-TYR-D-LEU-LEU-ARG-PRO-NHET;[DES-GLY10,DLEU6, PRONHET9] LH-RH LEUPROLIDE;Leuprolide; LHRH ethylamide;5-oxo-L-prolyl-L-histidyl-L-tryptophyl-L-seryl-L-tyrosyl-D-leucyl-L-leucyl-L-arginyl-N-ethyl-L-prolinamide;Carcinil;des-Gly10 ethylamide]gonadotropin releasing hormone;Enantone;GLP-HIS-TRP-SER-TYR-DLEU-LEU-ARG-PRO-NHET: GLP-HWSY-DL-LRP-NHET;Leuplin;LEUPROPELIN;Lucrin;nghormone;pGlu-His-Trp-Ser-Tyr-D-Leu-Leu-Arg-Pro-NHC2H5;Luteinizinghormone-releasing factor (pig),6-D-leucine-9-(N-ethyl-L-prolinamide)-10-deglycinamide-;(D-Leu6,des-Gly-NH210)-LH-RH ethylamide;A43818;D-Leu6-des-Gly10-LH-releasing hormone ethylamide;Des-Gly10-[D-Leu6]-LH-releasing hormone ethylamide;Des-Gly10-[D-Leu6]LH-RHethylamide;1-9-Luteinizinghormone-releasing factor (swine), 6-D-leucine-9-(N-ethyl-L-prolinamide)-;Lupron SR;NSC 377526;1: PN: WO02087616 PAGE: 31 claimed protein;Lupron;Leuprolide acetate salt;Prostap;Lutrate;Onectyl;Enanton;leuprolide-acetate;DSSTox_RID_83201;DSSTox_CID_28935;DSSTox_GSID_49009;MLS000028695;RGLRXNKKBLIBQS-XNHQSDQCSA-N;Tox21_113507;SMR00005894
SMILES: CC(O)=O.NC(N)=NCCC[C@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](CC1=CC=C(O)C=C1)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](CC2N=CNC=2)NC(=O)[C@H]3NC(=O)CC3)CC4C5=C(C=CC=C5)NC=4)C(=O)N6[C@@H](CCC6)C(=O)NCC
Formula: C61H88N16O14
M.Wt: 1269.4502
Purity: >98%
Sotrage: 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO
Description: Leuprolide is an agonist at pituitary GnRH receptors. Target: GnRH receptorLeuprorelin is a gonadotrophin-releasing hormone (GnRH) analogue used to treat a wide range of sex hormone-related disorders including advanced prostatic cancer, endometriosis and precocious puberty. Leuprorelin acts primarily on the anterior pituitary, inducing a transient early rise in gonadotrophin release. With continued use, Leuprorelin causes pituitary desensitisation and/or down-regulation, leading to suppressed circulating levels of gonadotrophins and sex hormones. [1] By interrupting the normal pulsatile stimulation of, and thus desensitizing, the GnRH receptors, it indirectly downregulates the secretion of gonadotropins luteinizing hormone (LH) and follicle-stimulating hormone (FSH), leading to hypogonadism and thus a dramatic reduction in estradiol and testosterone levels in both sexes. [2]
References: [1]. Plosker GL, Leuprorelin. A review of its pharmacology and therapeutic use in prostatic cancer, endometriosis and other sex hormone-related disorders. Drugs.1994 Dec;48(6):930-967. [2]. Leuprorelin
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