化合物 TG4-155|T5482|TargetMol

TG4-155
1164462-05-8

￥297 1mg 起订

￥433 2mg 起订

￥739 5mg 起订

上海更新日期：2024-09-30

TargetMol中国（陶术生物）

VIP3年

联系人：邵小姐

手机：4008200310 拨打

邮箱：marketing@tsbiochem.com

产品详情:

中文名称：: 化合物 TG4-155

英文名称：: TG4-155

CAS号：: 1164462-05-8

品牌：: TargetMol

产地：: 美国

保存条件：: Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.

纯度规格：: 97.20%

产品类别：: 抑制剂

货号：: T5482

Product Introduction

Bioactivity

Name	TG4-155
Description	TG4-155 is a brain penetrant EP2 antagonist (KB = 2.4 nM) that is over 1000-fold less effective at EP4 (KB = 11.4 μM) and a panel of other receptors and channels
Cell Research	Cytotoxicity of TG4-155 was examined with the CellTiter-Glo Luminescent Cell Viability Assay by measuring cellular ATP level, which correlates with cell viability.?Briefly, C6G cells were plated in 384-well plates at 2,000 cells/well in 25 μl DMEM plus test compound and incubated for 2 days.?CellTiter-Glo reagent (25 μl) was then added to each well.?The contents were mixed for 2 minutes on an orbital shaker to induce cell lysis and incubated at room temperature for 10 minutes.?Relative viability is proportional to luminescence intensity as measured by a microplate reader with an integration time of 1 second[2].
Animal Research	C57BL/6 mice (8 12 wk old) were injected with pilocarpine (280 mg/kg, i.p.) to induce status epilepticus (SE). SE was allowed for 1 h and terminated by pentobarbital (30 mg/kg, i.p.). Mice were then randomized by assignment to a random number stream and received two doses of vehicle or TG4-155 (5 mg/kg, i.p.) at 1 and 12 h after SE termination. Mice were euthanized under deep isoflurane anesthesia 24 h after SE and brains were collected for histology[1].
In vitro	TG4-155是一种能穿透大脑的EP2拮抗剂（KB=2.4 nM），其对EP4的效果降低超过1000倍（KB=11.4 μM），并且对一系列其他受体和通道[1]的作用也较低。
In vivo	TG4-155在由山梨醇引发的癫痫持续状态小鼠模型中显著减少神经退行性变化。该化合物抑制了经布他前列素[2]处理的癌细胞中的增殖、侵袭及炎症细胞因子表达。
Storage	Powder: -20°C for 3 years \| In solvent: -80°C for 1 year \| Shipping with blue ice.
Solubility Information	DMSO : 125 mg/mL (316.89 mM)
Keywords	inhibit \| TG4-155 \| TG-4-155 \| TG4155 \| TG4 155 \| Prostaglandin Receptor \| Inhibitor
Inhibitors Related	Rutin \| Tebufelone \| Evodiamine \| Benorilate \| p-Hydroxycinnamic acid \| Rebamipide \| Ethamsylate \| Tranilast \| Angoroside C \| Ozagrel \| Timapiprant \| Pranoprofen
Related Compound Libraries	Inhibitor Library \| Bioactive Compound Library \| Anti-Cancer Compound Library \| Bioactive Compounds Library Max \| Anti-Aging Compound Library \| Endocrinology-Hormone Compound Library \| NO PAINS Compound Library \| GPCR Compound Library \| Membrane Protein-targeted Compound Library \| Pain-Related Compound Library

TG4-155|TargetMol

TargetMol Chemicals Inc. 总部位于马萨诸塞州波士顿，致力于为全球生化领域科学家的研究提供专业的产品和服务。TargetMol?品牌的客户群分布于40多个国家和地区，已发展成为全球知名的化合物库和小分子化合物研究供应商。 TargetMol?可提供160多种满足不同需求的化合物库，以及多种类型的生化试剂产品，包括12000多种抑制剂、16000多种天然产物和各类多肽、抗体、生命科学试剂盒等，此外，我们还建设有CADD（计算机辅助药物设计）研究中心、药理实验室、药化合成平台三大技术中心，全方位满足客户的定制需求。凭借我们优质的产品和服务、快速高效的全球供应链和专业的技术支持，我们将有效帮助您缩短研发周期，取得更成功的结果。

成立日期	(12年)
注册资本	566.265100万人民币
员工人数	100-500人
年营业额	￥ 1亿以上
经营模式	贸易,工厂,试剂,定制,服务
主营行业	天然产物,生化试剂,分子生物学,分子砌块,生物技术服务

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