MGAT2-IN-2

MGAT2-IN-2 Suppliers list
Company Name: TargetMol Chemicals Inc.
Tel: +17819995354
Email: marketing@targetmol.com
Products Intro: Product Name:MGAT2-IN-2
CAS:1710630-11-7
Purity:98.00% Package:100 mg;500 mg Remarks:REAGENT;FOR LABORATORY USE ONLY
Company Name: TargetMol Chemicals Inc.
Tel:
Email: support@targetmol.com
Products Intro: Product Name:MGAT2-IN-2
CAS:1710630-11-7
Package:50mg;2580USD|25mg;1970USD|100mg;3400USD
Company Name: TargetMol Chemicals Inc.
Tel: +17819995354
Email: marketing@targetmol.com
Products Intro: Product Name:MGAT2-IN-2
CAS:1710630-11-7
Package:50mg;2580USD|25mg;1970USD|100mg;3400USD
Company Name: Fan De(Beijing) Biotechnology Co., Ltd.  
Tel: 15911056312
Email: liming@bio-fount.com
Products Intro: Product Name:MGAT2-IN-2
CAS:1710630-11-7
Purity:97.0% Package:5mg
Company Name: TargetMol Chemicals Inc.  
Tel: 4008200310
Email: marketing@tsbiochem.com
Products Intro: Product Name:MGAT2-IN-2
CAS:1710630-11-7
Package:50mg/RMB 18300;25mg/RMB 13900;100mg/RMB 23500

MGAT2-IN-2 manufacturers

  • MGAT2-IN-2
  • MGAT2-IN-2 pictures
  • $2580.00 / 50mg
  • 2024-10-24
  • CAS:1710630-11-7
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  • Purity:
  • Supply Ability: 10g
MGAT2-IN-2 Basic information
Product Name:MGAT2-IN-2
Synonyms:MGAT2-IN-2;1H-Indole-1-carboxamide, 5-[[(2,4-difluorophenyl)amino]sulfonyl]-2,3-dihydro-7-(2-oxo-1-pyrrolidinyl)-N-[4-(trifluoromethyl)phenyl]-;MGAT-2-IN-2,MGAT2IN2,MGAT2 IN 2
CAS:1710630-11-7
MF:C26H21F5N4O4S
MW:580.53
EINECS:
Product Categories:
Mol File:1710630-11-7.mol
MGAT2-IN-2 Structure
MGAT2-IN-2 Chemical Properties
density 1.567±0.06 g/cm3(Predicted)
storage temp. Store at -20°C
solubility Soluble in DMSO
pka8.81±0.20(Predicted)
Safety Information
MSDS Information
MGAT2-IN-2 Usage And Synthesis
UsesMGAT2-IN-2 is a potent and selective acyl CoA:monoacylglycerol acyltransferase 2 (MGAT2) inhibitor with an IC50 of 3.4 nM.
in vivo

Effect of MGAT2-IN-2 on plasma TG is elevated during the oral fat tolerance test in C57BL/6J mice. MGAT2-IN-2 (3, 10 and 30 mg/kg) is orally administered 6 h prior to oil challenge. Pharmacokinetic studies reveal that MGAT2-IN-2 displays a high plasma concentration (AUC0-8h=842 ng?h/mL) and favorable oral bioavailability (F=52%), which are probably driven by the improved stability against oxidative metabolism and hydrolysis. For evaluating the in vivo efficacy, MGAT2-IN-2 is examined for its effect on hypertriglyceridemia during oral fat tolerance test (OFTT) using C57BL/6J mice. To inhibit the hydrolysis of plasma triacylglycerol (TG) by lipoprotein lipase (LPL), mice are pretreated with an LPL inhibitor, Pluronic F127, permitting measurement of the accumulation of plasma TG following olive oil administration. MGAT2-IN-2 and vehicle are administered 6 h before the oral olive oil load, and plasma chylomicron TG concentrations are monitored for 4 h. MGAT2-IN-2 effectively and dose-dependently suppresses plasma TG elevation after olive oil challenge. The TG-lowering effect of MGAT2-IN-2 is significant (p<0.025) at doses of 10 and 30 mg/kg. A similar effect of reducing the rate of fat entrance into the circulation is observed in MGAT2 gene knockout mice[1].

IC 50MGAT2: 3.4 nM (IC50)
References[1] Sato K, et al. Discovery of a Novel Series of N-Phenylindoline-5-sulfonamide Derivatives as Potent, Selective, and Orally Bioavailable Acyl CoA:Monoacylglycerol Acyltransferase-2 Inhibitors. J Med Chem. 2015 May 14;58(9):3892-909. DOI:10.1021/acs.jmedchem.5b00178
[2] Sato K, et al. Optimization of a novel series of N-phenylindoline-5-sulfonamide-based acylCoA:monoacylglycerol acyltransferase-2 inhibitors: Mitigation of CYP3A4 time-dependent inhibition and phototoxic liabilities. Bioorg Med Chem. 2015 Aug 1;23(15):4544-60. DOI:10.1016/j.bmc.2015.06.003
MGAT2-IN-2 Preparation Products And Raw materials
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