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Nastorazepide

    
≥98%

Nastorazepide

源叶(MedMol)
S84361 一键复制产品信息
209219-38-5
C29H36N4O5
520.6199
Benzoic acid,3-(((((3R)-5-cyclohexyl-1-(3,3-dimethyl-2-oxobutyl)-2,3,4,5-tetrahydro-2-oxo-1H-1,5-benzodiazepin-3-yl)amino)carbonyl)amino)-; Nastorazepide; R-(-)-Z-360 Free acid; Z-360 free acid;
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
S84361-1mg促销
≥98%

¥400.00 ¥360.00

10 - - - -
S84361-5mg促销
≥98%

¥1000.00 ¥900.00

10 - - - -
S84361-10mg促销
≥98%

¥2200.00 ¥1980.00

9 - - - -
S84361-25mg促销
≥98%

¥4000.00 ¥3600.00

2 - - - -
S84361-50mg促销
≥98%

¥5700.00 ¥5130.00

3 - - - -
S84361-100mg促销
≥98%

¥8000.00 ¥7200.00

1 - - - -
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: Nastorazepide is a selective, orally available antagonist of gastrin/cholecystokinin 2 (CCK-2) receptor with potential antineoplastic activity.
靶点: cholecystokinin
体外研究: Nastorazepide binds to the gastrin/CCK-2 receptor, thereby preventing receptor activation by gastrin, a peptide hormone frequently associated with the proliferation of gastrointestinal and pancreatic tumor cells
体内研究: Nastorazepide significantly inhibits the growth of subcutaneous xenografts of human pancreatic tumor cells in mice, and that Nastorazepide combined with gemcitabine prolonged survival in a pancreatic carcinoma orthotopic xenograft mice
参考文献: 1. Kato H, et al. CCK-2/gastrin receptor signaling pathway is significant for gemcitabine-induced gene expression of VEGF in pancreatic carcinoma cells. Life Sci. 2011 Oct 24;89(17-18):603-8.
溶解性: Soluble  in  DMSO
保存条件: -20℃
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 1.921 ml 9.604 ml 19.208 ml
5 mM 0.384 ml 1.921 ml 3.842 ml
10 mM 0.192 ml 0.96 ml 1.921 ml
50 mM 0.038 ml 0.192 ml 0.384 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

质量 (mg) = 浓度 (mM) x 体积 (mL) x 分子摩尔量 (g/mol)

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