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Cetrorelix Acetate

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Chemical Structure| 145672-81-7 同义名 : SB-75 acetate;Cetrorelix (acetate);SB-75
CAS号 : 145672-81-7
货号 : A530148
分子式 : C72H94ClN17O15
纯度 : 99%
分子量 : 1473.075
MDL号 : MFCD08459466
存储条件:

粉末 Keep in dark place,Inert atmosphere,Store in freezer, under -20°C

液体 -20°C:3-6个月-80°C:12个月

溶解度 :

DMSO: 50 mg/mL(33.94 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO

H2O: 2 mg/mL(1.36 mM),配合低频超声助溶

动物实验配方:
生物活性
描述 Gonadotropin releasing hormone is the hypothalamic hormone that activates pituitary gonadotropin production and, ultimately, determines reproductive competence[3]. The gonadotropin-releasing hormone receptor (GnRHR) is a guanine nucleotide-binding protein-coupled receptor with a characteristic seven transmembrane domain motif. It transduces the hypothalamic message carried by the decapeptide gonadotropin-releasing hormone. At the gonadotrope cell surface the hormone binds to the receptor, leading to pituitary synthesis and secretion of gonadotropins. These glycoprotein hormones, in turn, modulate folliculogenesis and ovulation in the ovary[4].Cetrorelix Acetate (SB-75 acetate) is a potent gonadotropin-releasing hormone (GnRH) receptor antagonist with an IC50 of 1.21 nM [5].Treatment with Cetrorelix inhibited growth and colony-forming ability of myeloma cells, including cell lines resistant to arsenic trioxide, bortezomib, or lenalidomide. Cetrorelix induced apoptosis in myeloma cells including primary myeloma cells. In addition, Cetrorelix inhibited the growth of human myeloma cells xenografted into mice without any apparent side effects. Cetrorelix downregulated the nuclear factor-kappa B (NF-κB) pathway activity and the expression of cytokines, including interleukin 6, insulin-like growth factor 1, VEGF-A, and stromal-derived factor 1, important for myeloma cell growth and survival in myeloma cells and/or marrow stromal cells from myeloma patients. Cetrorelix decreased the phosphorylation of extracellular signal regulated kinase 1/2 and STAT3 in myeloma cells, two crucial pathways for myeloma cells growth and survival. Moreover, the expression of p21 and p53 was increased, whereas that of antiapoptotic proteins Bcl-2 and Bcl-x(L) was reduced by Cetrorelix[6].
实验方案
1mg 5mg 10mg

1 mM

5 mM

10 mM

0.68mL

0.14mL

0.07mL

3.39mL

0.68mL

0.34mL

6.79mL

1.36mL

0.68mL

参考文献

[1]Telegdy G, Tanaka M, et al. Effects of the LHRH antagonist Cetrorelix on the brain function in mice. Neuropeptides. 2009 Jun;43(3):229-34.

[2]Grundker C, Emons G. Role of gonadotropin-releasing hormone (GnRH) in ovarian cancer. Reprod Biol Endocrinol. 2003 Oct 7;1:65.

[3] Micol S Rothman,Margaret E Wierman. The role of gonadotropin releasing hormone in normal and pathologic endocrine processes. Curr Opin Endocrinol Diabetes Obes. 2007 Aug;14(4):306-10.

[4] D P Cohen . Molecular evaluation of the gonadotropin-releasing hormone receptor. Semin Reprod Med. 2000;18(1):11-6.

[5] Beckers T et al. Characterization of gonadotropin-releasing hormone analogs based on a sensitive cellular luciferase reporter gene assay. Anal Biochem. 1997 Aug 15;251(1):17-23.

[6]Jianguo Wen,et al. Luteinizing Hormone-Releasing Hormone (LHRH)-I antagonist cetrorelix inhibits myeloma cell growth in vitro and in vivo.Mol Cancer Ther. 2011 Jan;10(1):148-58.