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Quinagolide hydrochloride

    
≥99%

Quinagolide hydrochloride

源叶(MedMol)
S87466 一键复制产品信息
94424-50-7
C20H34ClN3O3S
432.02
盐酸喹高莱;(3S,4aS,10aR)-3-(二乙基氨磺酰氨基)-6-羟基-1-丙基-3,4,4a,5,10,10a-六氢-2H-苯并[g]喹啉盐酸盐;QUINAGOLIDE HYDROCHLORIDE;(3S,4aS,10aR)-3-(Diethylsulfamoylamino)-6-hydroxy-1-propyl-3,4,4a,5,10,10a-hexahydro-2H-benzo[g]qu
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
S87466-5mg
≥99%

¥2800.00

货期:2-3天 - - - -
S87466-10mg
≥99%

¥4100.00

货期:2-3天 - - - -
产品介绍 参考文献 质检证书(COA) 摩尔浓度计算器 相关产品
产品描述: Quinagolide hydrochloride (CV205-502 hydrochloride) is a selective and orally active dopamine D2 receptor agonist. Quinagolide hydrochloride is an inhibitor of prolactin. Quinagolide hydrochloride down-regulates AKT levels and its phosphorylation. Quinagolide hydrochloride shows antitumor effects, it can be used for the research of cancer
靶点: Dopamine Receptor;Akt
体内研究: Quinagolide hydrochloride (0.03-0.6 mg/kg; s.c. once daily for 2 month) effectively inhibits tumor growth in vivo. Animal Model: Female Wistar-Furth rats bearing SMtTW tumors Dosage: 0.03-0.6 mg/kg Administration: Subcutaneous injection; 0.03-0.6 mg/kg once daily for 2 month Result: Induced normalization of plasma PRL levels in all animals, reduced the tumor size compared with the control group at a dose of 0.3 mg/kg. Showed maximal inhibitory effects on PRL secretion and tumor growth at a dose of 0.3 mg/kg.
参考文献: 1. Trouillas J, et al. Inhibitory effects of the dopamine agonists quinagolide (CV 205-502) and bromocriptine on prolactin secretion and growth of SMtTW pituitary tumors in the rat. Endocrinology. 1994 Jan;134(1):401-10. 2. Iampietro C, et al. Quinagolide Treatment Reduces Invasive and Angiogenic Properties of Endometrial Mesenchymal Stromal Cells. Int J Mol Sci. 2022 Feb 4;23(3):1775.
溶解性: Soluble  in  DMSO
保存条件: 2-8℃
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 2.315 ml 11.574 ml 23.147 ml
5 mM 0.463 ml 2.315 ml 4.629 ml
10 mM 0.231 ml 1.157 ml 2.315 ml
50 mM 0.046 ml 0.231 ml 0.463 ml
注意: 部分产品我司仅能提供部分信息,我司不保证所提供信息的权威性,仅供客户参考交流研究之用。

参考文献

质检证书(COA)

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摩尔浓度计算器

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