基本信息 产品详情 公司简介 推荐产品
网站主页 化工产品目录 生物化工 生化试剂 激动剂抑制剂 ENCENICLINE 化合物 Encenicline
  • 化合物 Encenicline|T7193|TargetMol

化合物 Encenicline|T7193|TargetMol

Encenicline
550999-75-2
538 1mg 起订
1310 5mg 起订
1690 10mg 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 Encenicline
英文名称:
Encenicline
CAS号:
550999-75-2
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.
产品类别:
抑制剂
货号:
T7193

Product Introduction

Bioactivity

名称Encenicline
描述Encenicline (EVP-6124) is a selective α7 nicotinic acetylcholine receptor (nAChRs) agonist in development for treating cognitive impairment in schizophrenia and Alzheimer's disease.
细胞实验Experiments were carried out with human a7 nAChRs expressed in Xenopus laevis oocytes.?Oocytes were prepared, injected with cDNA encoding a7 nAChR subunits, and recorded using standard procedures.?Additional studies were carried out with rat a3b4, a4b2, and muscle a1b1gd nAChRs expressed in oocytes.?Briefly, ovaries were harvested from X. laevis females that were deeply anesthetized by cooling at 4℃ and with tricaine mesylate (3-aminobenzoic acid ethyl ester, methane sulfonate salt, 150 mg/l).?Small pieces of ovary were isolated in sterile Barth solution (88 mM NaCl, 1 mM KCl, 2.4 mM NaHCO3, 10 mM HEPES, 0.82 mM MgSO4·7H2O, 0.33 mM Ca(NO3)2·4H2O, and 0.41 mM CaCl2·6H2O, pH 7.4) and supplemented with 20 mg/ml kanamycin, 100 μg/ml penicillin, and 100 mg/ml streptomycin.?Injections of cDNAs encoding for the receptors were performed in at least one hundred oocytes using an automated ?injection device;?and receptor expression was examined at least two days later.?Oocytes were impaled with two electrodes filled with 3 M KCl, and their membrane potentials were ?maintained at ?80 mV throughout the experiment.?All recordings were performed ?at 18 C and cells were superfused with OR2 medium (82.5 mM NaCl, 2.5 mM KCl, 5 mM HEPES, 1.8 mM CaCl2·2H2O, and 1 mM MgCl2·6H2O, pH 7.4).?Currents were recorded using an automated process equipped with standard two-electrode voltage-clamp configuration.Data were captured and analyzed using Matlab or Excel software.ACh and EVP-6124 were prepared as concentrated stock solutions in water and then diluted in the recording medium to obtain the desired test concentrations.?All experiments were carried out using three or more cells[1].
动物实验For the experiments using natural forgetting (a 24 h retention interval) and MLA, twenty-four 2-month-old male Wistar rats .?In the doseeresponse experiment, the rats were 2.5 months old (average body weight: 319 g). For the coadministration of EVP-6124 and MLA , the rats were 3 months old (average body weight: 357 g). For the co-administration of EVP-6124 and MLA, the rats were 4 months old (average body weight: 407 g). Across the 3 experiments, rats were tested a total of 5e10 times.?The effects of EVP-6124 on memory consolidation in particular were investigated in the natural forgetting test in the ORT, using twentyfour 3-month-old Wistar rats (average body weight: 357 g). All 24 rats received each treatment, i.e. each rat was tested 7 times in two experiments.?All animals were housed individually, which improves ORT performance, in standard type III Makrolon cages on sawdust bedding.?The animals were on a reversed 12/12-h light/dark cycle (lights on from 19:00 to 7:00 h);?and food and water were given ad libitum.?The rats were housed and tested in the same room.?A radio, playing softly provided background noise to mask noises in the room.?All testing was performed between 9:00 and 18:00 h under low illumination (20 lux)[1].
体外活性In co-application experiments of EVP-6124 with acetylcholine, sustained exposure to EVP-6124 in functional investigations in oocytes caused desensitization at concentrations greater than 3 nM, while lower concentrations (0.3-1 nM) caused an increase in the acetylcholine-evoked response.?These actions were interpreted as representing a co-agonist activity of EVP-6124 with acetylcholine on α7 nAChRs.?The concentrations of EVP-6124 that resulted in physiological potentiation were consistent with the free drug concentrations in brain that improved memory performance in the ORT[2].
体内活性EVP-6124 showed selectivity for α7 nAChRs and did not activate or inhibit heteromeric α4β2 nAChRs.?EVP-6124 had good brain penetration and an adequate exposure time.?EVP-6124 (0.3 mg/kg) significantly restored memory function in scopolamine-treated rats (0.1 mg/kg) in an object recognition task (ORT).?Although donepezil at 0.1 mg/kg, p.o. or EVP-6124 at 0.03 mg/kg, p.o. did not improve memory in this task, co-administration of these sub-efficacious doses fully restored memory.?In a natural forgetting test, an ORT with a 24 h retention time, EVP-6124 improved memory at 0.3 mg/kg, This improvement was blocked by the selective α7 nAChR antagonist methyllycaconitine (0.3 mg/kg or 10 μg)[1].
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 : 60 mg/mL (187.01 mM)
关键字inhibit | nAChR | Nicotinic acetylcholine receptors | EVP 6124 | Encenicline | EVP6124 | Inhibitor
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 | 神经信号分子库 | NO PAINS 化合物库 | 膜蛋白靶向化合物库 | 神经退行性疾病化合物库 | 疼痛相关化合物库 | 人代谢物化合物库
EVP-6124|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 Encenicline相关厂家报价 更多

内容声明
拨打电话 立即询价