Sergliflozin etabonate
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Systematic (IUPAC) name | |
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2-(4-methoxybenzyl)phenyl 6-O-(ethoxycarbonyl)-β-D-glucopyranoside
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Clinical data | |
Routes of administration |
Oral |
Identifiers | |
CAS Number | 408504-26-7 |
ATC code | none |
PubChem | CID: 9824918 |
IUPHAR/BPS | 4587 |
ChemSpider | 21234810 |
ChEMBL | CHEMBL450044 |
Chemical data | |
Formula | C23H28O9 |
Molecular mass | 448.463 g/mol |
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Sergliflozin etabonate (INN/USAN,[1][2] codenamed GW869682X) is an investigational anti-diabetic drug being developed by GlaxoSmithKline. It did not undergo further development after phase II.[citation needed]
Method of action
Sergliflozin inhibits subtype 2 of the sodium-glucose transport proteins (SGLT2), which is responsible for at least 90% of the glucose reabsorption in the kidney. Blocking this transporter causes blood glucose to be eliminated through the urine.[3][4]
Chemistry
Etabonate refers to the ethyl carbonate group. The remaining structure, which is the active substance, is called sergliflozin.
References
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- ↑ Prous Science: Molecule of the Month November 2007
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Categories:
- Chemical articles having calculated molecular weight overwritten
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- SGLT2 inhibitors
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