Home Metabolism AdipoR agonist AdipoRon For research use only.

AdipoRon

Synonyms: SC-396658

AdipoRon (SC-396658) is a novel, and orally bioavailable adiponectin receptor agonist with KD of 1.8 and 3.1 μM for AdipoR1 and AdipoR2, respectively.

AdipoRon Chemical Structure

AdipoRon Chemical Structure

CAS: 924416-43-3

Selleck's AdipoRon has been cited by 11 Publications

1 Customer Review

Purity & Quality Control

Batch: Purity: 99.96%
99.96

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Biological Activity

Description AdipoRon (SC-396658) is a novel, and orally bioavailable adiponectin receptor agonist with KD of 1.8 and 3.1 μM for AdipoR1 and AdipoR2, respectively.
Features Orally bioavailable adiponectin receptor agonist that can be used for the treatment of obesity-related diseases.
Targets
AdipoR1 [1] AdipoR2 [1]
1.8 μM(Kd) 3.1 μM(Kd)
In vitro
In vitro AdipoRon increases AMPK activation, PGC-1α expression and mitochondrial biogenesis by binding to both AdipoR1 and AdipoR2 in C2C12 myotubes. [1]
In Vivo
In vivo In skeletal muscle and liver of wild-type mice AdipoRon (50 mg/kg, i.v.) significantly induces phosphorylation of AMPK via AdipoR1 and AdipoR2. In WT mice, AdipoRon (50 mg/kg, p.o.) improves insulin resistance, glucose intolerance and dyslipidaemia by activating AdipoR1–AMPK–PGC-1α pathways in skeletal muscle, while by activating AdipoR2–PPAR-α pathways in the liver. Moreover, AdipoRon ameliorates diabetes of genetically obese rodent model db/db mice, and prolongs the shortened lifespan of db/db mice on a high-fat diet. [1]

Chemical lnformation & Solubility

Molecular Weight 428.52 Formula

C27H28N2O3
CAS No. 924416-43-3 SDF Download AdipoRon SDF
Smiles C1CN(CCC1NC(=O)COC2=CC=C(C=C2)C(=O)C3=CC=CC=C3)CC4=CC=CC=C4
Storage (From the date of receipt)

In vitro
Batch:

DMSO : 100 mg/mL ( (233.36 mM)； Moisture-absorbing DMSO reduces solubility. Please use fresh DMSO.)

Ethanol : 50 mg/mL

Water : Insoluble


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In vivo
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Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )

Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.

Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.

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Tech Support

Answers to questions you may have can be found in the inhibitor handling instructions. Topics include how to prepare stock solutions, how to store inhibitors, and issues that need special attention for cell-based assays and animal experiments.

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