CAS 220810-26-4|(Des-Gly10,D-His(Bzl)6,Pro-NHEt9)-LHRH acetate salt
| Common Name | (Des-Gly10,D-His(Bzl)6,Pro-NHEt9)-LHRH acetate salt | ||
|---|---|---|---|
| CAS Number | 220810-26-4 | Molecular Weight | 1323.50 (free base) |
| Density | / | Boiling Point | / |
| Molecular Formula | C66H86N18O12.xC2H4O2 | Melting Point | / |
| MSDS | / | Flash Point | / |
Names
| Name | histrelin acetate |
|---|
BiologicalActivity
| Description | Histrelin acetate, a GnRH analogue, is a GnRH Receptor agonist. Histrelin acetate increases serum luteinising hormone (LH), follicle stimulating hormone (FSH) and testosterone levels. Histrelin acetate can be used in the research of prostate cancer, endometriosis[1][2][5]. |
|---|---|
| Related Catalog | Signaling Pathways >>GPCR/G Protein >>GNRH ReceptorResearch Areas >>Cancer |
| References | [1]. Emma D Deeks, et al. Histrelin: in advanced prostate cancer. Drugs. 2010 Mar 26;70(5):623-30. [2]. Marlena Juszczak, et al. Hypothalamic gonadotropin-releasing hormone receptor activation stimulates oxytocin release from the rat hypothalamo-neurohypophysial system while melatonin inhibits this process. Brain Res Bull. 2010 Jan 15;81(1):185-90. [3]. P E Cohen, et al. Colony-stimulating factor-1 plays a major role in the development of reproductive function in male mice. Mol Endocrinol. 1997 Oct;11(11):1636-50. [4]. D W Hahn, et al. Development of an animal model for quantitatively evaluating effects of drugs on endometriosis. Fertil Steril. 1985 Sep;44(3):410-5. [5]. E Boczek-Leszczyk, et al. Vasopressin release from the rat hypothalamo-neurohypophysial system: effects of gonadotrophin-releasing hormone (GnRH), its analogues and melatonin. J Physiol Pharmacol. 2010 Aug;61(4):459-66. |
Chemical & Physical Properties
| Molecular Formula | C66H86N18O12.xC2H4O2 |
|---|---|
| Molecular Weight | 1323.50 (free base) |
| Exact Mass | 1442.71000 |
| PSA | 521.46000 |
| LogP | 3.97960 |
| InChIKey | OWAUGAMNPZHEOJ-YKZVIGSYSA-N |
| SMILES | CC(=O)O.CCNC(=O)C1CCCN1C(=O)C(CCCN=C(N)N)NC(=O)C(CC(C)C)NC(=O)C(Cc1cn(Cc2ccccc2)cn1)NC(=O)C(Cc1ccc(O)cc1)NC(=O)C(CO)NC(=O)C(Cc1c[nH]c2ccccc12)NC(=O)C(Cc1cnc[nH]1)NC(=O)C1CCC(=O)N1 |
