
TGR5
CAS No. 1197300-24-5
TGR5( TGR5 Receptor Agonist | MDK00245 | MDK-00245 | MDK 00245 )
Catalog No. M10702 CAS No. 1197300-24-5
TGR5 Receptor Agonist, a potent TGR5(GPCR19) agonist, showed improved potency in the U2-OS cell assay (pEC50 = 6.8) and in melanophore cells (pEC50 = 7.5).
Purity : >98% (HPLC)






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Biological Information
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Product NameTGR5
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NoteResearch use only, not for human use.
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Brief DescriptionTGR5 Receptor Agonist, a potent TGR5(GPCR19) agonist, showed improved potency in the U2-OS cell assay (pEC50 = 6.8) and in melanophore cells (pEC50 = 7.5).
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DescriptionTGR5 Receptor Agonist, a potent TGR5(GPCR19) agonist, showed improved potency in the U2-OS cell assay (pEC50 = 6.8) and in melanophore cells (pEC50 = 7.5).
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In Vitro——
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In VivoTGR5 Receptor Agonist (CCDC) activates directly a sub-population of bladder-innervating dorsal root ganglia (DRG) neurons and a small percentage of non-neuronal cells in Trpv1-/- mice.?TGR5 Receptor Agonist (CCDC) (2?or 5 μg; ICV) reduces food intake and body weight in diet-induced obese mice. Animal Model:Female C57BL/6J mice [12-18 weeks; TRPV1 knockout (trpv1-/-), TRPA1 knockout (trpa1-/-), or TGR5 knockout (Gpbar1-/-)]Dosage:100 μM, 100 μL Administration:Infused gently, to fill but not fully distend the bladder, and allowed to incubate for 5 minResult:Activated directly a sub-population of bladder-innervating dorsal root ganglia (DRG) neurons in Trpv1-/- mice, also activated a small percentage of non-neuronal cells.Increased intracellular Ca2+ in bladder-innervating DRG neurons.Increased intracellular Ca2+ in a small proportion of non-neuronal cells.Animal Model: Male C57BL/6J mice (obese induced by high-fat diet)Dosage:2?or 5 μg at a volume of 0.2 μL per brain side and a rate of 0.6 μL/min Administration:ICV (acute intra-hypothalamic experiment) Result:Significantly reduced food intake over time, with a robust reduction in 24 h food intake and body weight gain.Animal Model:Male C57BL/6J mice (obese induced by high-fat diet; implanted with micro-osmotic pumps that were filled with CCDC)Dosage:5 μg/day; 91.9 μL, pumping rate of 0.09 μL/h Administration:ICV; for 4 weeks (chronic experiment) Result:Reduced food intake and improved insulin responsiveness.Increased energy expenditure during the dark phase.Increased mRNA expression of β1, 2, and 3 adrenoreceptors (Adrb1, Adrb2, and Adrb3) in the epidydimal white adipose tissue, and increased Dio2 (the gene expressing the enzyme D2) in brown adipose tissue.
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SynonymsTGR5 Receptor Agonist | MDK00245 | MDK-00245 | MDK 00245
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PathwayGPCR/G Protein
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TargetGPCR19
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RecptorTGR5
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Research AreaMetabolic Disease
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Indication——
Chemical Information
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CAS Number1197300-24-5
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Formula Weight361.22
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Molecular FormulaC18H14Cl2N2O2
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Purity>98% (HPLC)
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SolubilityDMSO, Ethanol: 100 mM
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SMILESO=C(C1=C(C)ON=C1C2=CC=CC=C2Cl)N(C3=CC=C(Cl)C=C3)C
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Chemical Name3-(2-chlorophenyl)-N-(4-chlorophenyl)-N,5-dimethyl-4-isoxazolecarboxamide
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1.Evans KA, et al. J Med Chem. 2009 Dec 24;52(24): 7962-5.
molnova catalog



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