An SGLT2 inhibitor and active metabolite of dapagliflozin
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Parent Compound(s)
11574Dapagliflozin
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Information provided in the product description is from published literature. Due to the nature of scientific experimentation, your results (e.g., selectivity and effective concentrations) or specific application for this product may differ. If you have questions about how this product fits your application, please contact our technical support staff.

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O-desethyl Dapagliflozin

Item No. 36022

Technical Information
Formal Name
(1S)-1,5-anhydro-1-C-[4-chloro-3-[(4-hydroxyphenyl)methyl]phenyl]-D-glucitol
CAS Number
864070-37-1
Molecular Formula
C19H21ClO6
Formula Weight
Purity
≥98%
A crystalline solid
DMF: 30 mg/mlDMSO: 30 mg/mlEthanol: 30 mg/mlEthanol:PBS (pH 7.2) (1:1): 0.5 mg/ml
SMILES
O[C@H]([C@H]1O)[C@H](C(C=C2)=CC(CC(C=C3)=CC=C3O)=C2Cl)O[C@@H]([C@H]1O)CO
InChi Code
InChI=1S/C19H21ClO6/c20-14-6-3-11(8-12(14)7-10-1-4-13(22)5-2-10)19-18(25)17(24)16(23)15(9-21)26-19/h1-6,8,15-19,21-25H,7,9H2/t15-,16-,17+,18-,19+/m1/s1
InChi Key
ODQAIMBPQWETBE-FQBWVUSXSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Wet ice in continental US; may vary elsewhere
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    Product Description

    O-desethyl Dapagliflozin is an inhibitor of sodium-glucose cotransporter 2 (SGLT2; IC50 = 9.4 nM) and active metabolite of dapagliflozin (Item No. 11574).1,2 It is selective for SGLT2 over SGLT1 (IC50 = 970 nM).1

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Xu, B., Feng, Y., Cheng, H., et alC-aryl glucosides substituted at the 4'-position as potent and selective renal sodium-dependent glucose co-transporter 2 (SGLT2) inhibitors for the treatment of type 2 diabetes. Bioorg. Med. Chem. Lett. 21(15), 4465-4470 (2011).

    2. Xu, G., Lv, B., Roberge, J.Y., et alDesign, synthesis, and biological evaluation of deuterated C-aryl glycoside as a potent and long-acting renal sodium-dependent glucose cotransporter 2 inhibitor for the treatment of type 2 diabetes. J. Med. Chem. 57(4), 1236-1251 (2014).