Sergliflozin etabonate
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Routes of administration | Oral |
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Formula | C23H28O9 |
Molar mass | 448.468 g·mol−1 |
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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.
![](http://upload.wikimedia.org/wikipedia/commons/thumb/5/5f/Sergliflozin_skeletal.svg/220px-Sergliflozin_skeletal.svg.png)
Sergliflozin
References[]
- ^ World Health Organization (2008). "International Nonproprietary Names for Pharmaceutical Substances (INN). Recommended International Nonproprietary Names: List 59" (PDF). WHO Drug Information. 22 (1): 66.
- ^ "Statement on a nonproprietary name adopted by the USAN council: Sergliflozin etabonate" (PDF). American Medical Association. Retrieved 2008-08-10.
- ^ Katsuno K, Fujimori Y, Takemura Y, et al. (January 2007). "Sergliflozin, a novel selective inhibitor of low-affinity sodium glucose cotransporter (SGLT2), validates the critical role of SGLT2 in renal glucose reabsorption and modulates plasma glucose level". J Pharmacol Exp Ther. 320 (1): 323–30. doi:10.1124/jpet.106.110296. PMID 17050778. S2CID 8306408.
- ^ Prous Science: Molecule of the Month November 2007
Categories:
- Drugs not assigned an ATC code
- SGLT2 inhibitors
- Glucosides
- Prodrugs
- Phenol ethers
- Abandoned drugs
- Gastrointestinal system drug stubs