Chemodex

Phloridzin

CHF 41.00
In stock
CDX-P0263-M250250 mgCHF 41.00
CDX-P0263-G0011 gCHF 68.00
More Information
Product Details
Synonyms Floridzin; Phloretin 2'-glucoside; Phloridzosid; Phlorizin; NSC 2833
Product Type Chemical
Properties
Formula

C21H24O10

MW 436.413
CAS 60-81-1
RTECS UC2080000
Source/Host Chemicals Plant
Purity Chemicals ≥98% (HPLC)
Appearance Light yellow to off-white powder.
Solubility Soluble in DMSO (20mg/ml), DMF (20mg/ml) or ethanol (5mg/ml).
Identity Determined by 1H-NMR.
Declaration Manufactured by Chemodex.
Other Product Data

Click here for Original Manufacturer Product Datasheet
Our product description may differ slightly from the original manufacturers product datasheet.

InChi Key IOUVKUPGCMBWBT-RQUKQETFSA-N
Smiles OC1=CC=C(CCC(C2=C(O)C=C(O)C=C2O[C@@H]3[C@@H](O)[C@H](O)[C@@H](O)[C@H](CO)O3)=O)C=C1
Shipping and Handling
Shipping AMBIENT
Short Term Storage +20°C
Long Term Storage -20°C
Handling Advice Protect from light and moisture.
Use/Stability Stable for at least 2 years after receipt when stored at -20°C.
Documents
MSDS Download PDF
Product Specification Sheet
Datasheet Download PDF
Description

Phlorizin is a natural product, first isolated from the bark of apple trees, that reduces plasma glucose levels by blocking renal and intestinal glucose absorption through inhibition of SGLT1 and SGLT2. It competitively inhibits (competes with D-glucose) the initial rate of α-methyl-D-glucopyranoside (α-MDG) uptake in the nM range. Phlorizin has been shown to enhance insulin sensitivity and to have antioxidant properties. Sodium-glucose cotransporter 1 (SGLT1) is a high affinity, low capacity transporter abundant in the small intestine, with some expression in the kidney as well. SGLT2 is a low affinity, high capacity transporter in the kidney that accounts for approximately 90% of glucose reabsorption into the blood stream. Selective inhibition of SGLT2 is a potential strategy for reducing plasma glucose levels as a treatment for diabetes.

Product References

(1) G. Toggenburger, et al.; Biochim. Biophys. Acta 688, 557 (1982) | (2) N. Oulianova, et al.; J. Membr. Biol. 179, 223 (2001) | (3) K.P. Briski & E.S. Marshall; Neurochem. Res. 26, 783 (2001) | (4) R.J. McCrimmon, et al.; Am. J. Physiol. Endocrinol. Metab. 283, E1076 (2002) | (5) J.R.L. Ehrenkranz, et al.; 21, 31 (2005) (Review) | (6) J.R. White; Clin. Diabet. 28, 5 (2010) | (7) C.S. Hummel, et al.; Am. J. Phys. cell Phys. 300, C14 (2011) | (8) C.S. Hummel, et al.; Am. J. Phys. cell Phys. 302, C373 (2012) | (9) T. Nagata, et al.; Am. J. Physiol. Renal. Physiol. 306, F1520 (2014) | (10) Y. Katsuda, et al.; Exp. Anim. 64, 161 (2015) | (11) M. Raja & R.K. Kinne; Biochimie 115, 187 (2015) | (12) X. Mei, et al.; J. Agric. Food Chem. 64, 7502 (2016) | (13) R.A. Mendes, et al.; J. Mol. Model 24, 101 (2018)

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