ChemicalBook--->CAS DataBase List--->2922283-43-8

2922283-43-8

2922283-43-8 Structure

2922283-43-8 Structure
IdentificationBack Directory
[Name]

2,1-Benzisoxazole-5-carboxylic acid, 3-[1,1′-biphenyl]-4-yl-
[CAS]

2922283-43-8
[Synonyms]

2,1-Benzisoxazole-5-carboxylic acid, 3-[1,1′-biphenyl]-4-yl-
[Molecular Formula]

C20H13NO3
[MOL File]

2922283-43-8.mol
[Molecular Weight]

315.32
Chemical PropertiesBack Directory
[Boiling point ]

599.2±35.0 °C(Predicted)
[density ]

1.299±0.06 g/cm3(Temp: 20 °C; Press: 760 Torr)(Predicted)
[solubility ]

DMSO: Slightly soluble: 0.1-1 mg/ml
[form ]

Solid
[pka]

3.62±0.30(Predicted)
[color ]

Light yellow to yellow
Hazard InformationBack Directory
[Uses]

UNC7467 is a potent IP6K inhibitor with values of 4.9, 8.9 and 1320 nM for IP6K2, IP6K1 and IP6K6, respectively. UNC7467 reduces levels of inositol pyrophosphates. UNC7467 can be used for obesity research[1].
[in vivo]

UNC7467 (5 mg/kg; i.p.; daily, for 4 weeks; diet-induced obesity mice) ameliorated diet induced obesity, insulin resistance, and hepatic steatosis[1].
UNC7467 (1-5 mg/kg; i.v. and i.p.; diet-induced obesity mice) exhibits low clearance (13.7 (mL/min)/kg) and large AUClast (6054 h?ng/mL for intra venous (i.v.) and 2527 h?ng/mL for intraperitoneal (i.p.)) in mice at 5 mg/kg dose[1].

Animal Model:Diet-induced obesity (DIO) mice[1]
Dosage:5 mg/kg
Administration:Intraperitoneal injection; daily, for 4 weeks
Result:Improved glycemic profiles, ameliorated hepatic steatosis, and reduced weight gain without altering food intake.
Animal Model:Diet-induced obesity (DIO) mice[1]
Dosage:5 mg/kg (Pharmacokinetic Analysis)
Administration:Intravenous injection and intraperitoneal injection
Result:1.19
routeivip
Dose (mg/kg)55
AUClast (h*ng/mL)60542527
CL (mL/min/kg)13.7
[References]

[1] Zhou Y, et, al. Development of Novel IP6K Inhibitors for the Treatment of Obesity and Obesity-Induced Metabolic Dysfunctions. J Med Chem. 2022 May 12;65(9):6869-6887. DOI:10.1021/acs.jmedchem.2c00220
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