ChemicalBook--->CAS DataBase List--->92933-48-7

92933-48-7

92933-48-7 Structure

92933-48-7 Structure
IdentificationBack Directory
[Name]

5-Butyl-1H-pyrazole-3-carboxylic acid
[CAS]

92933-48-7
[Synonyms]

LUF6283
5-Butyl-1H-pyrazole-3-carboxylic acid
3-butyl-1H-pyrazole-5-carboxylic acid
1H-Pyrazole-3-carboxylic acid, 5-butyl-
[Molecular Formula]

C8H12N2O2
[MDL Number]

MFCD16620107
[MOL File]

92933-48-7.mol
[Molecular Weight]

168.19
Chemical PropertiesBack Directory
[Melting point ]

166-167 °C
[Boiling point ]

385.8±30.0 °C(Predicted)
[density ]

1?+-.0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[solubility ]

DMSO: soluble10mg/mL (clear solution; warmed)
[form ]

powder
[pka]

15.44±0.10(Predicted)
[color ]

white to beige
Safety DataBack Directory
[WGK Germany ]

3
Hazard InformationBack Directory
[Description]

LUF6283 is a partial agonist of GPR109A/HCA2 G protein-coupled receptors (Ki = 0.55 μM in a radioligand binding assay). It stimulates [35S]-GTPγS binding and increases phosphorylation of ERK in HEK293T cells expressing GPR109A/HCA2 receptors (EC50s = 3.1 and 0.32 μM, respectively). In vivo, LUF6283 (400 mg/kg per day) reduces plasma levels of VLDL and hepatic expression of apolipoprotein B in mice.
[Uses]

LUF 6283 is a partial agonist of HCA2 and is a promising drug candidate to achieve a beneficial lipid lowering effect of niacin, ultimately treating dyslipidemic disorders.
[in vivo]

LUF6283 (C57BL/6 mice, 400 mg/kg, Oral gavage, once a day for 4 weeks) has no effect on adipose tissue ATGL/HSL expression, and significantly reduces the expression of apolipoprotein B (APOB)[1].

[References]

[1] ZHAOSHA LI. Effects of pyrazole partial agonists on HCA2-mediated flushing and VLDL-triglyceride levels in mice[J]. British Journal of Pharmacology, 2012, 167 4: 818-825. DOI: 10.1111/j.1476-5381.2012.02039.x
Spectrum DetailBack Directory
[Spectrum Detail]

5-Butyl-1H-pyrazole-3-carboxylic acid(92933-48-7)1HNMR
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