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网站主页 化工产品目录 生物化工 抑制剂 神经信号通路(Neuronal Signaling) AChR 调节剂 PNU 120596 化合物 PNU120596
  • 化合物 PNU120596|T6950|TargetMol

化合物 PNU120596|T6950|TargetMol

PNU-120596
501925-31-1
273 5mg 起订
462 10mg 起订
888 25mg 起订
上海 更新日期:2024-12-12

TargetMol中国(陶术生物)

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邮箱:marketing@tsbiochem.com

产品详情:

中文名称:
化合物 PNU120596
英文名称:
PNU-120596
CAS号:
501925-31-1
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:
98.34%
产品类别:
抑制剂
货号:
T6950

Product Introduction

Bioactivity

名称PNU-120596
描述PNU-120596 (NSC-216666) is a positive allosteric modulator of α7 nAChR with EC50 of 216 nM.
细胞实验SH-SY5Y-α7 cells are plated on 96-well plates at a density of 15,000 cells per well (100 μL of 1.5 × 105 cells per mL) in complete growth medium and placed into a 37 °C incubator for 20 to 24 hours. Complete growth medium then is replaced with experimental medium alone ("PNU-120596 free") or containing appropriate concentrations of PNU-120596 and returns to the 37 °C ncubator for 20 to 24 hours. The medium is then replaced with fresh experimental medium and 20 μL per well MTS solution and returned to the 37 °C incubator for 3 hours, after which the plate is read on a microplate spectrophotometer at an absorbance of 490 nm. For all data analysis, data are normalized to untreated compound-free wells (100% cell viability) and a background absorbance taken from wells containing experimental medium and MTS solution.(Only for Reference)
激酶实验Ca2+ Fluorescence Assay: SH-EP1 human epithelial cells expressing a variant of theα7 nAChR (α7*) are grown in minimal essential medium (MEM) containing nonessential amino acids supplemented with 10% fetal bovine serum, L-glutamine, 100 U/ml penicillin/streptomycin, 250 ng/mL fungizone, 400 μg/mL hygromycin B, and 800 μg/mL geneticin. α7* is a variant of the human α7 nAChR, with two point mutations in the first transmembrane domain (T230P and C241S) that allow for high functional expression in SH-EP1 cells [Groppi VE, Wolfe ML, Berkenpas MB (2003) U.S. Patent 6,693,172 B1]. Cells are grown in a 37 °C incubator with 6% CO2. Cells are trypsinized and plated in 96-well plates with dark side walls and clear bottoms at a density of 2 × 104 cells/well 2 days before analysis. Cells are loaded with a mixture of Calcium reen-1AM in anhydrous dimethylsulfoxide and 20% pluronic F-127. This reagent is added directly to the growth medium of each well to achieve a final concentration of 2 μM Calcium Green-1 AM. Cells are then incubated in the dye for 1 hour at 37 °C and then washed four times with Mark's modified Earle's balanced salt solution (MMEBSS) composed of the following (inmM): 4 CaCl2, 0.8 MgSO4, 20 NaCl, 5.3 KCl, 5.6 D-glucose, 20 Tris-HEPES, and 120 N-methyl-D-glucamine, pH 7.4. After the fourth cycle, the cells are allowed to incubate at 37 °C for at least 10 minutes. The final volume of MMEBSS in each well is 100 μL and atropine is added to all wells for a final concentration of 1 μM. A fluorometric imaging plate reader (FLIPR; Molecular Devices, Union City, CA) is set up to excite Calcium Green at 488 nm using 500 mW of power and reading fluorescence emission of >525 nm. A 0.5 seconds exposure is used to illuminate each well. Fluorescence is detected using an F-stop set of either 2.0 or 1.2. After 30 seconds of baseline recording, test compounds are added to each well of a 96-well plate in 50 μL of a 3 × stock.In each experiment, four wells are used as vehicle (0.2% DMSO) controls.
动物实验Animal Models: male Sprague Dawley rats (weighing 250–300 g)Formulation: PNU-120596 is dissolved in 5% DMSO and 5% Solutol in PBS.Dosages: 1 mg/kgAdministration: PNU-120596 is intravenously administrated 5 minutes before auditory gating measurements.
体外活性PNU-120596通过增强由人类α7 nAChR工程变体介导的乙酰胆碱(Ach)激发的钙通量,以及通过野生型受体介导的乙酰胆碱和胆碱激发的电流,并在拟南芥卵母细胞中的激动剂持续存在时显著延长激发反应。PNU-120596能增加α7 nAChRs的通道平均开启时间,但对离子选择性无影响,对单位电导率的影响极小。当应用于急性海马切片时,PNU-120596增加了在锥体神经元中测量的ACh激发的GABAergic突触后电流的频率;该效果被TTX抑制,表明PNU-120596调节位于海马区星形细胞树突膜上的α7 nAChRs的功能。除了对α7 nAChR的正向调节外,PNU-120596还显著延缓了脱敏动力学,增加了通过过度刺激α7 nAChR引起的Ca2+诱导的毒性的潜力。PNU-120596还改变了与α7 nAChR结合时内部β折叶、转换区和激动剂结合位点的半胱氨酸可达性。PNU-120596的结合位点不在激动剂结合位点,并通过引起与由Ach促进的门控构象相似但非完全相同的构象效应来增强烟碱型受体激动剂激发的门控。
体内活性系统性给药PNU-120596(1 mg/kg)给大鼠可改善由安非他明引起的听觉闸门缺陷,这一模型被提出用来反映与精神分裂症相关的电路级干扰。[1] 在卡拉胶之前给予PNU-1230596,30 mg/kg显著减轻了机械性痛觉过敏和承重缺陷,效果持续达4小时。PNU-120596减弱了由卡拉胶引起的TNF-α和IL-6在后爪水肿中的增加水平,而双氯芬酸仅减轻了IL-6水平。通过卡拉胶或CFA引起的已建立的机械性痛觉过敏也被PNU-120596部分逆转。[4]
存储条件Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
溶解度DMSO : 31.2 mg/mL (100 mM)
关键字pain | anti-hyperalgesia | inhibit | inflammatory | Nicotinic acetylcholine receptors | TNF-α | Inhibitor | α7nAChR | disorders | PNU 120596 | neurological | NSC216666 | IL-6 | nAChR | PNU120596 | PNU-120596 | NSC-216666
相关产品Pilocarpine Hydrochloride | Levamisole hydrochloride | Choline chloride | Pilocarpine nitrate | CLOZAPINE N-OXIDE | Pempidine | Forskolin | (+)-Sparteine | Propoxur | Adiphenine hydrochloride | Ribavirin | Nanofin
相关库经典已知活性库 | 已知活性化合物库 | 抗阿尔茨海默症化合物库 | 神经递质受体化合物库 | NO PAINS 化合物库 | 离子通道库 | 神经退行性疾病化合物库 | 膜蛋白靶向化合物库 | 疼痛相关化合物库 | 表型筛选靶点鉴定库
NSC 216666|TargetMol

公司简介

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

化合物 PNU120596相关厂家报价

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  • 2024-09-26
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  • PNU-120596
  • PNU-120596
  • 上海贝昶生物科技有限公司
  • 2023-06-09
  • 询价
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