CU-CPT-8m (Synonyms: TLR8-specific antagonist)
目录号: PL12309 纯度: ≥99%
CAS No. :125079-83-6
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中文名称
CU-CPT-8m
中文别名
7-(间甲苯基)吡唑并[1,5-A]嘧啶-3-甲酰胺;化合物CU-CPT-8M
英文名称
CU-CPT-8m
英文别名
Pyrazolo[1,5-a]pyrimidine-3-carboxamide, 7-(3-methylphenyl)-;CU-CPT-8m;7-(m-tolyl)pyrazolo[1,5-a]pyrimidine-3-carboxamide;CPD1578;cas 125079-83-6;CU-CPT-8M;CAS 125079-83-6 ;TLR8 INHIBITOR;TLR8-specific antagonist
Cas No.
125079-83-6
分子式
C14H12N4O
分子量
252.27
包装储存
Powder -20°C 3 years;4°C 2 years
产品详情
CU-CPT-8m 是 TLR8 的特异性拮抗剂,其 IC50 值为 67 nM。
生物活性
CU-CPT-8m is a specific TLR8 antagonist, with an IC 50 of 67 nM.
性状
Solid
IC50 & Target[1][2]
TLR8 67 nM (IC50)
体外研究(In Vitro)
CU-CPT-8m is a specific TLR8 antagonist, with an IC50 of 67±10 nM and negligible cytotoxicity. The Kd value of CU-CPT-8m is determined to be 220 nM. CU-CPT-8m only reduces the proinflammatory response in the TLR8-overexpressing cells strongly supports that CU-CPT-8m directly recognizes TLR8 in cells. It is particularly notable that TLR7 signaling is not affected at concentrations up to 75 μM. TLR7 and TLR8 are closely related and share many common ligands. Treatment of 1 μM CU-CPT-8m completely abolishes the elevation of TNF-α and IL-8 mRNA levels induced by R848. CU-CPT-8m inhibits R848-induced TNF-α production in the differentiated THP-1 monocytes cells in a dose-dependent manner with an IC50 of 90±10 nM, which is in good agreement with its IC50 value determined in HEK-Blue TLR8 cells.
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Powder -20°C 3 years;4°C 2 years
参考文献
[1]. Zhang S, et al. Small-molecule inhibition of TLR8 through stabilization of its resting state. Nat Chem Biol. 2018 Jan;14(1):58-64.
溶解度数据
In Vitro: DMSO : 12.5 mg/mL (49.55 mM; ultrasonic and warming and heat to 60°C)配制储备液
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1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

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