化合物 ARN 272,ARN272

化合物 ARN 272|T5357|TargetMol

价格 125 197 347
包装 2mg 5mg 10mg
最小起订量 1mg
发货地 上海
更新日期 2025-11-17
QQ交谈 微信洽谈

产品详情

中文名称:化合物 ARN 272英文名称:ARN272
CAS:488793-85-7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/Shipping at ambient temperature.
产品类别: 抑制剂
货号: T5357
2025-11-17 化合物 ARN 272 ARN272 2mg/125RMB;5mg/197RMB;10mg/347RMB 125 TargetMol 美国 Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. 抑制剂

Product Introduction

Bioactivity

名称ARN272
描述ARN272 is a FAAH-like anandamide transporter (FLAT) inhibitor (IC50: 1.8 μM).
动物实验All rats were surgically implanted with intra-oral cannula under isoflurane anaesthesia. Following recovery from surgery (3 days), rats received a single adaptation trial to habituate them to the chamber and the infusion procedure. During the adaptation trial, rats were placed individually in the TR chamber and received a 2?min intra-oral infusion of water (reverse osmosis water infused at 1?mL/min). On the following day, rats received the first of two conditioning trials (separated by 72?h). On each conditioning trial, rats received a pretreatment injection of ARN272 or VEH 120?min prior to the conditioning trials. During conditioning trails, rats were intra-orally infused with a saccharin solution (0.1%) for 2?min (1?mL/min) and orofacial and somatic reactions were recorded on video. Immediately following the saccharin infusion, the rats were injected with LiCl (0.15?M) or saline, and then returned to their home cage. Two additional groups were added (after ARN272 at 3.0?mg·kg?1 attenuated gaping) where pretreatment of ARN272 at 3.0?mg·kg?1 or VEH was given 120?min prior, and with SR141716 30?min prior, to each conditioning trial. The groups were VEH-Saline (VEH-SAL), n = 9; VEH-LiCl, n = 8; 0.1?mg/kg ARN272-LiCl, n = 9; 1.0?mg/kg ARN272-LiCl, n = 8; 3.0?mg/kg ARN272-LiCl, n = 8; 1.0?mg/kg SR-3.0?mg/kg ARN272, n = 8; 1.0?mg/kg SR-VEH, n = 8. Seventy-two hours following the second conditioning trial, the rats received a drug-free TR test. During the TR test, rats were re-exposed to a 2?min intra-oral infusion of saccharin solution and their orofacial and somatic responses again recorded. All video recordings were later scored by a rater blind to the experimental conditions using ‘The Observer'. Following the TR test, the rats were returned to their home cages and at 16:00?h, their water bottles were removed to begin a water deprivation regime in preparation for the CTA test.At 08:00?h the following morning, the rats received a one-bottle test in which a graduated tube of 0.1% saccharin solution was placed on the home cage, and the amount consumed was recorded at 30 and 120?min intervals. A one-bottle test was used as there is evidence to suggest it is more sensitive in detecting between-group differences in strength of taste avoidance than a two-bottle test where both water and saccharin are made available [2].
体外活性ARN272对FLAT的抑制似乎是选择性的,因为这种化合物对几种内源性大麻素代谢酶几乎没有或没有抑制作用。此外,ARN272对大鼠脑FAAH活性的抑制作用弱且不完全,且在与重组人FAAH-1孵育后不被显著水解(在37°C下孵育24小时后的水解率约为5%)[1]。
体内活性在小鼠体内,通过腹腔注射ARN272(1mg/kg)能够提高血浆中阿纳米酰胺(anandamide)的水平,而不影响2-AG、OEA或PEA的水平。研究指出,ARN272抑制阿纳米酰胺在体外内化和在体内失活的效应,以及在faah-1/ 小鼠中观察到的阿纳米酰胺积聚减少现象[1]。ARN272的系统性给药在大鼠中产生了剂量依赖性地抑制因恶心引起的条件性张口行为,并在鼩鼱中减少了呕吐的剂量依赖性降低。在大鼠中,与ARN272(3.0mg/kg)的系统性共同给药能完全逆转ARN272以1.0mg/kg抑制的张口行为。SR141716单独使用的效果与载体溶液无差异[2]。
存储条件Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
溶解度H2O : Insoluble
10% DMSO+40% PEG300+5% Tween 80+45% Saline : 2 mg/mL (4.62 mM), Sonication is recommended.
Ethanol : 8 mg/mL (18.5 mM), Sonication is recommended.
DMSO : 50 mg/mL (115.61 mM), Sonication is recommended.
关键字Inhibitor | inhibit | FAAH | ARN-272 | ARN272
相关产品2-Chlorophenylboronic acid | Drinabant | AM281 | PF 750 | β-Caryophyllene | Pregnenolone acetate | 2,3-Butanediol | CB1 antagonist 2 | Biochanin A | Dehydroabiethylamine | Pregnenolone | CB2 modulator 1
相关库抑制剂库 | 脂代谢化合物库 | 经典已知活性库 | 已知活性化合物库 | 代谢化合物库 | 神经信号分子库 | NO PAINS 化合物库 | 抗肥胖化合物库 | 抗代谢疾病化合物库
关键字: ARN 272|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 2013-04-18 (13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
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 经营模式 贸易,工厂,试剂,定制,服务
  • TargetMol中国(陶术生物)
VIP 4年
  • 公司成立:13年
  • 注册资本:566.265100万人民币
  • 企业类型:有限责任公司(自然人投资或控股)
  • 主营产品:小分子抑制剂、药物筛选化合物库、药物筛选等
  • 公司地址:静安区江场三路238号8楼
询盘

化合物 ARN 272|T5357|TargetMol相关厂家报价

产品名称 价格   公司名称 报价日期
询价
VIP4年
湖北海克斯生化有限公司
2025-12-29
询价
VIP6年
陕西缔都医药化工有限公司
2025-09-11
询价
碧云天生物技术有限公司
2025-12-28
¥1499.90
VIP2年
上海阿拉丁生化科技股份有限公司
2025-05-16
内容声明:
以上所展示的信息由商家自行提供,内容的真实性、准确性和合法性由发布商家负责。 商家发布价格指该商品的参考价格,并非原价,该价格可能随着市场变化,或是由于您购买数量不同或所选规格不同而发生变化。最终成交价格,请咨询商家,以实际成交价格为准。请意识到互联网交易中的风险是客观存在的
主页 | 企业会员服务 | 广告业务 | 联系我们 | 旧版入口 | 中文MSDS | CAS Index | 常用化学品CAS列表 | 化工产品目录 | 新产品列表 |投诉中心
Copyright © 2008 ChemicalBook 京ICP备07040585号  京公海网安备110108000080号  All rights reserved.