ACH-000143
目录号: PL07083 纯度: ≥98%
CAS No. :2225836-30-4
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中文名称
ACH-000143
英文名称
ACH-000143
英文别名
N-[2-(5-Chloro-2,6-dimethoxy-1H-benzimidazol-1-yl)ethyl]acetamide;ACH-000143;BDBM463447;N-[2-(5-chloro-2,6-dimethoxybenzimidazol-1-yl)ethyl]acetamide
Cas No.
2225836-30-4
分子式
C13H16ClN3O3
分子量
297.74
包装储存
4°C, protect from light In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)
产品详情
ACH-000143 是有效的、具有口服活性的褪黑素受体的激动剂,对MT1 和MT2 的EC50 值分别为0.06 nM 和0.32 nM。
生物活性
ACH-000143 is a potent and orally active melatonin receptor agonist, with EC 50 values of 0.06 nM and 0.32 nM for MT1 and MT2, respectively.
性状
Solid
IC50 & Target[1][2]
MT1 0.06 nM (EC50) MT2 0.32 nM (EC50
体内研究(In Vivo)
ACH-000143 reduces liver triglycerides and steatosis in diet-Induced obese rats.
ACH-000143 is devoid of hERG binding, genotoxicity, and behavioral alterations at doses up to 100 mg/kg p.o., supporting further investigation of this compound as a drug candidate.
ACH-000143 significantly reduces plasma glucose at 10 mg/kg (?16.4%, p < 0.05) and 30 mg/kg (?16.9%, p < 0.01).
has not independently confirmed the accuracy of these methods. They are for reference only.
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
4°C, protect from light In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)
参考文献
[1]. Marcos Antonio Ferreira Jr, et al. Discovery of ACH-000143: A Novel Potent and Peripherally Preferred Melatonin Receptor Agonist that Reduces Liver Triglycerides and Steatosis in Diet-Induced Obese Rats. J Med Chem. 2021 Feb 25;64(4):1904-1929.
溶解度数据
In Vitro: DMSO : 50 mg/mL (167.93 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。

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