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TLR7/8 agonist 1 dihydrochloride

    
99.70%

1-(4-(Aminomethyl)benzyl)-2-butyl-1H-imidazo[4,5-c]quinolin-4-amine dihydrochloride

源叶(MedMol)
Y65418 一键复制产品信息
1620278-72-9
C22H27Cl2N5
432.39
TLR7/8 agonist-5d; TLR7/8 agonist5d; TLR7/8 agonist 5d
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
Y65418-1mg买3赠1
99.70%

¥390.00

8 - - - -
Y65418-5mg买3赠1
99.70%

¥550.00

6 - - - -
Y65418-10mg买3赠1
99.70%

¥740.00

6 - - - -
Y65418-25mg买3赠1
99.70%

¥980.00

3 - - - -
Y65418-100mg
≥98%

¥2850.00

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: TLR7/8 agonist 1 dihydrochloride is a toll-like receptor TLR7/TLR8 dual-agonistic imidazoquinoline
靶点: TLR7;TLR8;TLR
体外研究: TLR7/8 agonist 1 (Compound 5d) shows prominent immunostimulatory activities. TLR7/8 agonist 1 serves as a convenient precursor for the covalent attachment of fluorophores without significant loss of activity. TLR7/8 agonist 1 retains TLR7-agonistic activity with an EC50 of 20 nM. TLR7/8 agonist 1 (Compound 1) shows substantially different agonistic potencies in human TLR7 (50 nM) and TLR8 (55 nM) primary screens.
参考文献: 1. Shukla NM, et al. Syntheses of fluorescent imidazoquinoline conjugates as probes of Toll-like receptor 7. Bioorg Med Chem Lett. 2010 Nov 15;20(22):6384-6. 2. Beesu M, et al. Structure-Based Design of Human TLR8-Specific Agonists with Augmented Potency and Adjuvanticity. J Med Chem. 2015 Oct 8;58(19):7833-49.
溶解性: Soluble  in  DMSO
保存条件: -20°C
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 2.313 ml 11.564 ml 23.127 ml
5 mM 0.463 ml 2.313 ml 4.625 ml
10 mM 0.231 ml 1.156 ml 2.313 ml
50 mM 0.046 ml 0.231 ml 0.463 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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