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CB1 ANTAGONIST 2

    
99.90%

CB1 ANTAGONIST 2

源叶(MedMol)
S89309 一键复制产品信息
614726-85-1
C17H12Cl3N3O
380.653
AM4113;5-(4-Chlorophenyl)-1-(2,4-dichlorophenyl)-4-methylpyrazole-3-carboxamide
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
S89309-5mg买3赠1
99.90%

¥410.00

5 - - - -
S89309-10mg买3赠1
99.90%

¥670.00

5 - - - -
S89309-25mg促销
99.90%

¥1250.00 ¥1000.00

5 - - - -
S89309-100mg促销
99.90%

¥3900.00 ¥3120.00

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: CB1 antagonist 2 is caimabinoid 1 (CB1) antagonist extracted from patent WO2016184310A1, compound 3, inhibits CB1 in vivo with an IC50 of 25.5 nM
靶点: Cannabinoid Receptor;CannabinoidReceptor
体外研究: AM4113 was able to bind with high affinity to CB1 receptors, exhibiting 100-fold selectivity for CB1 against CB2 receptors. The Ki value for CB1 was 0.897 ± 0.44 nM, while the Ki value for hCB2 was 92 ± 6.9 nM .
体内研究: In rats, treatment with AM4113 (2.0 and 4.0 mg/kg) attenuated the AM411-induced locomotor suppression and analgesia. In addition, 4.0 mg/kg AM4113 alone significantly suppressed locomotor activity when compared with vehicle. AM4113 dose-dependently decreased lever pressing on an FR1 schedule. AM4113 produced conditioned taste avoidance and suppression of ingestive (hedonic) taste reactivity scores in a dose-dependent manner [1]. AM4113 didn’t induce signs of nausea .
参考文献: 1. Song Li, et al. 4-methyl-diaryl -1H- pyrazole derivatives and their use as medicamentsFIELD.
溶解性: Soluble  in  DMSO
保存条件: -20℃
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 2.627 ml 13.135 ml 26.271 ml
5 mM 0.525 ml 2.627 ml 5.254 ml
10 mM 0.263 ml 1.314 ml 2.627 ml
50 mM 0.053 ml 0.263 ml 0.525 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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