ChemicalBook--->CAS DataBase List--->1422365-52-3

1422365-52-3

1422365-52-3 Structure

1422365-52-3 Structure
IdentificationBack Directory
[Name]

HL271
[CAS]

1422365-52-3
[Synonyms]

HL271
HL271,HL-271
[Molecular Formula]

C13H17ClF3N5O
[MDL Number]

MFCD34470232
[MOL File]

1422365-52-3.mol
[Molecular Weight]

351.76
Chemical PropertiesBack Directory
[form ]

Solid
[color ]

White to off-white
Hazard InformationBack Directory
[Uses]

Lixumistat (HL271) hydrochloride (IM156 hydrochloride; HL156A hydrochloride), a chemical derivative of Metformin (HY-B0627), is a potent AMPK activator that increases AMPK phosphorylation. Lixumistat hydrochloride attenuates aging-associated cognitive impairment in animal model[1][2]. Lixumistat hydrochloride is a potent oxidative phosphorylation (OXPHOS) inhibitor which can be used for the research of solid tumors[3].
[in vivo]

Lixumistat (hydrochloride) does not affect metabolic regulation assessed by body weight, blood glucose, insulin levels and lipid metabolite content in mice with diet-induced obesity[1].
Lixumistat (hydrochloride) (50 mg/kg; for 2 months) does not affect body weight, general locomotion, or anxiety[2].
Lixumistat (hydrochloride) significantly attenuates the aging-induced decline in novel object recognition memory and spatial working memory[2].
Lixumistat (hydrochloride) significantly increases AMPK activation in the hippocampus of aged mice[2].

Animal Model:C57BL/6J mice (young group/12-16 weeks, old groups/20-22 months)[2]
Dosage:50 mg/kg
Administration:Oral administration (in drinking water), for 2 months
Result:Attenuated age-related cognitive decline.
[References]

[1] Row H, et al. HL271, a novel chemical compound derived from metformin, differs from metformin in its effects on the circadian clock and metabolism. Biochem Biophys Res Commun. 2016 Jan 15;469(3):783-9. DOI:10.1016/j.bbrc.2015.11.069
[2] Bang E, et al. The Improving Effect of HL271, a Chemical Derivative of Metformin, a Popular Drug for Type II Diabetes Mellitus, on Aging-induced Cognitive Decline. Exp Neurobiol. 2018 Feb;27(1):45-56. DOI:10.5607/en.2018.27.1.45
[3] Sun Young Rha, et al. Phase I study of IM156, a novel potent biguanide oxidative phosphorylation (OXPHOS) inhibitor, in patients with advanced solid tumors. Journal of Clinical Oncology 38(15_suppl):3590-3590.
1422365-52-3 suppliers list
Company Name: TargetMol Chemicals Inc.
Tel: +1-781-999-5354; +17819995354 , +17819995354
Website: https://www.targetmol.com/
Company Name: TargetMol Chemicals Inc.
Tel: +1-781-999-5354;
Website: https://www.targetmol.com/
Company Name: TargetMol Chemicals Inc.
Tel: +17819995354 , +17819995354
Website:
Company Name: Sichuan Wei Keqi Biological Technology Co., Ltd.  
Tel: 028-81700200 18116577057
Website: https://www.weikeqi-biotech.com/
Company Name: Shanghai Rechem science Co., Ltd.  
Tel: 021-31433387 15618786686
Website: cn.rechemscience.com
Company Name: Nantong QuanYi Biotechnology Co., Ltd  
Tel: 0513-66337626 18051384581
Website: https://www.chemhifuture.com/
Company Name: TargetMol Chemicals Inc.  
Tel: 15002134094
Website: https://www.targetmol.cn/
Tags:1422365-52-3 Related Product Information