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内吗啡肽 1

    
98%

Endomorphin 1

源叶(MedMol)
S84136 一键复制产品信息
189388-22-5
C34H38N6O5
610.7
MFCD01321063
TYR-PRO-TRP-PHE-NH2;H-Tyr-Pro-Trp-Phe-NH2; Tyr-Pro-Trp-Phe; Endomorphin 1;;Endomorphin 1
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
S84136-5mg促销
98%

¥454.00 ¥408.00

货期:3-5天 - - - -
S84136-10mg促销
98%

¥700.00 ¥630.00

8 - - - -
S84136-25mg促销
98%

¥1250.00 ¥1130.00

3 - - - -
S84136-100mg促销
98%

¥3700.00 ¥3330.00

3 - - - -
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: Endomorphin 1 is a high affinity and selective agonist of the μ-opioid receptor and displays reasonable affinities for kappa3 binding sites (Ki: 20~30 nM).
靶点: Opioid Receptor;OpioidReceptor
体内研究: Both Endomorphin 1 and Endomorphin 2 are potent analgesics with peak effects seen at 10 and 15 min, respectively. All subsequent studies are performed at peak effect. Both compounds are fully active supraspinally and spinally, with no indication of ceiling effects. Both Endomorphin 1 and Endomorphin 2 display a profile similar to morphine. Neither compound has analgesic activity in CXBK mice at a dose that produced over 70% analgesia in control CD-1 mice.
动物实验: Groups of mice are treated i.c.v. with Endomorphin 1 (12 μg) or Endomorphin 2 (3 μg) 15 min before a 0.5-cc charcoal meal (2.5% gum tragacanth,10% activated charcoal in water). The mice are killed 30 min later and the distance the charcoal traveled is measured.
参考文献: 1. Goldberg IE, et al. Pharmacological characterization of endomorphin-1 and endomorphin-2 in mouse brain. J Pharmacol Exp Ther. 1998 Aug;286(2):1007-13.
溶解性: Soluble  in  H2O
保存条件: -20℃
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 1.637 ml 8.187 ml 16.375 ml
5 mM 0.327 ml 1.637 ml 3.275 ml
10 mM 0.164 ml 0.819 ml 1.637 ml
50 mM 0.033 ml 0.164 ml 0.327 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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