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Phloretin (RJC 02792) SGLT inhibitor

Cat.No.S2342

Phloretin (RJC 02792, NSC 407292, Dihydronaringenin) is a dihydrochalcone found in apple tree leaves, and it shows beneficial effects on diabetes.
Phloretin (RJC 02792) SGLT inhibitor Chemical Structure

Chemical Structure

Molecular Weight: 274.27

Quality Control

Cell Culture, Treatment & Working Concentration

Cell Lines Assay Type Concentration Incubation Time Formulation Activity Description PMID
H1299 cells Function assay 30 mins Inhibition of GLUT1 in human H1299 cells assessed as inhibition of 2-deoxy-D-[3H]-glucose uptake incubated for 15 mins prior to 2-deoxy-D-[3H]-glucose addition measured after 30 mins by liquid scintillation counting analysis, IC50=21.4 Μm
PK15NTD cells Function assay Binding affinity to human recombinant CNT3 expressed in pig PK15NTD cells assessed as [3H]uridine uptake by beta-scintillation, Ki=32.28 μM
Click to View More Cell Line Experimental Data

Chemical Information, Storage & Stability

Molecular Weight 274.27 Formula

C15H14O5

Storage (From the date of receipt)
CAS No. 60-82-2 Download SDF Storage of Stock Solutions

Synonyms NSC 407292, Dihydronaringenin Smiles C1=CC(=CC=C1CCC(=O)C2=C(C=C(C=C2O)O)O)O

Solubility

In vitro
Batch:

DMSO : 55 mg/mL (200.53 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO.)

Ethanol : 55 mg/mL

Water : Insoluble

Molarity Calculator

Mass Concentration Volume Molecular Weight

In vivo
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Working concentration: mg/ml;

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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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Mechanism of Action

Targets/IC50/Ki
SGLT1 [1]
SGLT2 [1]
In vitro
Phloretin (RJC 02792) is a dihydrochalcone found in the bark of pear (Pyrus communis), apple, cherry and other fruit trees. It inhibits the active transport of glucose into cells by SGLT1 and SGLT2, though the inhibition is weaker than by its glycoside phlorizin. [1] Orally consumed phlorizin is nearly entirely converted into phloretin by hydrolytic enzymes in the small intestine. An important effect of this is the inhibition of glucose absorption by the small intestine and the inhibition of renal glucose reabsorption. [2] [3] This compound also inhibits a variety of urea transporters. It induces urea loss and diuresis when coupled with high protein diets. [4]
References

Clinical Trial Information

(data from https://clinicaltrials.gov, updated on 2024-05-22)

NCT Number Recruitment Conditions Sponsor/Collaborators Start Date Phases
NCT05073523 Completed
Healthy
Chalmers University of Technology
September 27 2021 Not Applicable

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