ChemicalBook--->CAS DataBase List--->2225836-30-4

2225836-30-4

2225836-30-4 Structure

2225836-30-4 Structure
IdentificationBack Directory
[Name]

Acetamide, N-[2-(5-chloro-2,6-dimethoxy-1H-benzimidazol-1-yl)ethyl]-
[CAS]

2225836-30-4
[Synonyms]

ACH-000143
Acetamide, N-[2-(5-chloro-2,6-dimethoxy-1H-benzimidazol-1-yl)ethyl]-
[Molecular Formula]

C13H16ClN3O3
[MDL Number]

MFCD34167540
[MOL File]

2225836-30-4.mol
[Molecular Weight]

297.74
Chemical PropertiesBack Directory
[density ]

1.34±0.1 g/cm3(Predicted)
[storage temp. ]

4°C, protect from light
[solubility ]

DMSO : 50 mg/mL (167.93 mM; Need ultrasonic)
[form ]

Solid
[pka]

15.77±0.46(Predicted)
[color ]

White to off-white
Hazard InformationBack Directory
[Uses]

ACH-000143 is a potent and orally active melatonin receptor agonist, with EC50 values of 0.06 nM and 0.32 nM for MT1 and MT2, respectively[1].
[Biological Activity]

ACH-000143 is a potent and orally active melatonin receptor agonist, with EC50 values of 0.06 nM and 0.32 nM for MT1 and MT2, respectively[1]. ACH-000143 reduces liver triglycerides and steatosis in diet-Induced obese rats[1].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[1].ACH-000143 significantly reduces plasma glucose at 10 mg/kg (-16.4%, p < 0.05) and 30 mg/kg (-16.9%, p < 0.01)[1].
[in vivo]

ACH-000143 reduces liver triglycerides and steatosis in diet-Induced obese rats[1].
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[1].
ACH-000143 significantly reduces plasma glucose at 10 mg/kg (?16.4%, p < 0.05) and 30 mg/kg (?16.9%, p < 0.01)[1].

Animal Model:High-fat diet rats[1].
Dosage:10 and 30 mg/kg.
Administration:Orally, once daily for two months.
Result:Significantly reduced the weekly BW gain on weeks.
[IC 50]

MT1: 0.06 nM (EC50); MT2: 0.32 nM (EC50)
[References]

[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.
Spectrum DetailBack Directory
[Spectrum Detail]

Acetamide, N-[2-(5-chloro-2,6-dimethoxy-1H-benzimidazol-1-yl)ethyl]-(2225836-30-4)1HNMR
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