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BAN ORL 24

    
≥96%

BAN ORL 24

源叶(MedMol)
S83119 一键复制产品信息
1401463-54-4
C27H37Cl2N3O2
506.5076
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
S83119-5mg
≥96%

¥650.00

货期:3-5天 - - - -
S83119-10mg
≥96%

¥1200.00

货期:3-5天 - - - -
S83119-50mg
≥96%

¥4180.00

货期:3-5天 - - - -
S83119-100mg
≥96%

¥7440.00

货期:3-5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: BAN ORL 24 is a nociceptin/orphanin FQ (N/OFQ) peptide receptor (NOP) antagonist. BAN ORL 24 has antagonistic effect for nociceptin (NOP) receptor with KI value of 0.24 nM in CHO cell. BAN ORL 24 can be used for the research of cancer and analgesic
靶点: Ki: 0.24 nM (NOP in CHO cell). IC50: 50 μM (NOR); 0.224 μM (MOR);Others
体外研究: BAN ORL 24 has antagonist for NOR and MOR (opioid receptor subtype) with IC50 values of 50 μM and 0.224 μM, respectively
体内研究: BAN ORL 24 (10 mg/kg; i.v.) attenuates the duration of BPRIM97 thermal antinociception. Animal Model: C57BL/6 mice Dosage: 10 mg/kg Administration: 10 mg/kg; i.v. Result: Caused inhibition of BPRIM97-induced antinociception at 90-min postinjection.Did not attenuate BPR1M97-induced antinociception in the tail-clip test after 30 min.
参考文献: 1. Fischetti et al (2009) Pharmacological characterization of the nociceptin/orphanin FQ receptor non peptide antagonist compound 24. Eur.J.Pharmacol. 614 50. 2. Tao Hou, et al. Label-free cell phenotypic study of opioid receptors and discovery of novel mu opioid ligands from natural products. J Ethnopharmacol 3. Chao, et al. BPR1M97, a dual mu opioid receptor/nociceptin-orphanin FQ peptide receptor agonist, produces potent antinociceptive effects with safer properties than morphine. Neuropharmacology 166, 107678 (2020).
溶解性: Soluble  in  DMSO、H2O
保存条件: -20℃
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 1.974 ml 9.872 ml 19.743 ml
5 mM 0.395 ml 1.974 ml 3.949 ml
10 mM 0.197 ml 0.987 ml 1.974 ml
50 mM 0.039 ml 0.197 ml 0.395 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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