CAS 220810-26-4|(Des-Gly10,D-His(Bzl)6,Pro-NHEt9)-LHRH acetate salt

Introduction:Basic information about CAS 220810-26-4|(Des-Gly10,D-His(Bzl)6,Pro-NHEt9)-LHRH acetate salt, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
Common Name(Des-Gly10,D-His(Bzl)6,Pro-NHEt9)-LHRH acetate salt
CAS Number220810-26-4Molecular Weight1323.50 (free base)
Density/Boiling Point/
Molecular FormulaC66H86N18O12.xC2H4O2Melting Point/
MSDS/Flash Point/

Names

Namehistrelin acetate

BiologicalActivity

DescriptionHistrelin 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 CatalogSignaling 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 FormulaC66H86N18O12.xC2H4O2
Molecular Weight1323.50 (free base)
Exact Mass1442.71000
PSA521.46000
LogP3.97960
InChIKeyOWAUGAMNPZHEOJ-YKZVIGSYSA-N
SMILESCC(=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
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