TG6-10-1
目录号: PL04684 纯度: ≥99%
CAS No. :1415716-58-3
商品编号 规格 价格 会员价 是否有货 数量
PL04684-5mg 5mg ¥1928.00 请登录
PL04684-10mg 10mg ¥2571.00 请登录
PL04684-50mg 50mg ¥11250.00 请登录
PL04684-100mg 100mg 询价 询价
PL04684-200mg 200mg 询价 询价
PL04684-10mM*1mLinDMSO 10mM*1mLinDMSO ¥2121.00 请登录
Medlife所售产品仅用于科学研究(非临床研究),非药品不可食用,不可用于人体或动物的临床诊断和治疗,我们不为个人提供产品及服务。产品COA等资料,可至下方“质量控制”中下载。
中文名称
TG6-10-1
中文别名
(2E)-N-[2-[2-(三氟甲基)-1H-吲哚-1-基]乙基]-3-(3,4,5-三甲氧基苯基)-2-丙烯酰胺
英文名称
TG6-10-1
英文别名
TG6-10-1;BCP16857;BDBM50016950;A15968;(E)-N-(2-(2-(Trifluoromethyl)-1H-indol-1-yl)ethyl)-3-(3,4,5-trimethoxyphenyl)acrylamide;(2E)-N-{2-[2-(trifluoromethyl)-1H-indol-1-yl]ethyl}-3-(3,4,5-trimethoxyphenyl)prop-2-enamide;(E)-N-[2-[2-(Trifluoromethyl)indol-1-yl]ethyl]-3-(3,4,5-trimethoxyphenyl)prop-2-enamide
Cas No.
1415716-58-3
分子式
C23H23F3N2O4
分子量
448.43
包装储存
Powder -20°C 3 years;4°C 2 years
产品详情
TG6-10-1 是一种 EP2 拮抗剂, 低纳摩尔下有效作用于 EP2, 比作用于人 EP3, EP4 和 IP 受体选择性高 300, EP1 受体选择性高 100 倍的。
生物活性
TG6-10-1 is an EP2 antagonist, shows low-nanomolar antagonist activity against only EP2, >300-fold selectivity over human EP3, EP4, and IP receptors, 100-fold selectivity over EP1 receptors.
性状
Solid
IC50 & Target[1][2]
EP2
体外研究(In Vitro)
TG6-10-1 robustly blocks prostaglandin E2 (PGE2) (10 μM)-induced cAMP accumulation in a concentration-dependent manner in SH-SY5Y cells. has not independently confirmed the accuracy of these methods. They are for reference only.
体内研究(In Vivo)
TG6-10-1 (5 mg/kg; i.p.; 4-30 hours) improves survival, accelerates recovery of lost weight, and improves functional recovery following status epilepticus (SE) . has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model:
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]. Jiang J, et al. Inhibition of the prostaglandin receptor EP2 following status epilepticus reduces delayed mortality and brain inflammation. Proc Natl Acad Sci U S A. 2013 Feb 26;110(9):3591-3596.
[2]. Kang X, et al. Cyclooxygenase-2 contributes to oxidopamine-mediated neuronal inflammation and injury via the prostaglandin E2 receptor EP2 subtype. Sci Rep. 2017 Aug 25;7(1):9459.
溶解度数据
In Vitro: DMSO : 100 mg/mL (223.00 mM; Need ultrasonic)配制储备液
搜索质检报告(COA)

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。

The molarity calculator equation
Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)
The dilution calculator equation
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
This equation is commonly abbreviated as: C1V1 = C2V2