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LOXIGLUMIDE

    
98.00%

LOXIGLUMIDE

源叶(MedMol)
S81873 一键复制产品信息
107097-80-3
C21H30Cl2N2O5
461.379
氯谷胺;Loxiglumide; LOXIGLUMIDE; Loxizin; CR-1505;
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
S81873-5mg促销
98.00%

¥170.00 ¥136.00

6 - - - -
S81873-10mg促销
98.00%

¥298.00 ¥238.00

6 - - - -
S81873-25mg促销
98.00%

¥590.00 ¥472.00

6 - - - -
S81873-50mg促销
≥98%

¥1090.00 ¥872.00

货期:2-3天 - - - -
S81873-100mg促销
≥98%

¥2130.00 ¥1700.00

货期:2-3天 - - - -
S81873-200mg
≥98%

¥2970.00

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: Loxiglumide is a cholecystokinin (CCK-1) receptor antagonist.
靶点: CCK-1 receptor;cholecystokinin
体内研究: The effects of pancreatic rest by oral administration of CCK-1 receptor antagonist Loxiglumide and pancreas stimulation are investigated via endogenous CCK release induced by po protease inhibitor camostat on the recovery of pancreatic secretory function, and biochemical and histological changes of the pancreas after acute hemorrhagic pancreatitis. Oral administration of CCK-1 receptor antagonist Loxiglumide with a dose of 50 mg/kg body weight inhibits pancreatic exocrine secretion for more than 12 h. Thus, every 12-h administration of Loxiglumide might have completely blocks the effect of endogenously released CCK on the pancreas (pancreatic rest)
参考文献: 1. Jia D, et al. Effect of endogenous cholecystokinin on the course of acute pancreatitis in rats. World J Gastroenterol. 2015 Jul 7;21(25):7742-53.
溶解性: DMSO  :  ≥  100  mg/mL  (216.74  mM)
保存条件: 2-8℃
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 2.167 ml 10.837 ml 21.674 ml
5 mM 0.433 ml 2.167 ml 4.335 ml
10 mM 0.217 ml 1.084 ml 2.167 ml
50 mM 0.043 ml 0.217 ml 0.433 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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