Remogliflozin etabonate
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Systematic (IUPAC) name | |
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5-methyl-4-[4-(1-methylethoxy)benzyl]-1-(1-methylethyl)-1H-pyrazol-3-yl 6-O-(ethoxycarbonyl)-β-D-glucopyranoside
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Clinical data | |
Routes of administration |
Oral |
Identifiers | |
CAS Number | 442201-24-3 ![]() |
ATC code | none |
ChemSpider | 8047110 |
UNII | TR0QT6QSUL ![]() |
KEGG | D10055 ![]() |
ChEMBL | CHEMBL494323 ![]() |
Chemical data | |
Formula | C26H38N2O9 |
Molecular mass | 522.586 g/mol |
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Remogliflozin etabonate (INN/USAN)[1] is a proposed drug of the gliflozin class for the treatment of type 2 diabetes, investigated by GlaxoSmithKline.[2] Remogliflozin is now being developed by BHV Pharma with Islet Sciences.[3]
Clinical trials
Remogliflozin etabonate (RE) was shown to enhance urinary glucose excretion in rodents and humans. Early studies in diabetics improved plasma glucose levels.[4][5] Remogliflozin etabonate has been studied at doses up to 1000 mg.[6] A pair of 12-week phase 2b randomized clinical trials of diabetics published in 2015, found reductions in glycated hemoglobin and that it was generally well tolerated.[7]
Method of action
Remogliflozin etabonate is a pro-drug of remogliflozin. Remogliflozin inhibits the sodium-glucose transport proteins (SGLT), which are responsible for glucose reabsorption in the kidney. Blocking this transporter causes blood glucose to be eliminated through the urine.[8] Remogliflozin is selective for SGLT2.
See also
References
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- ↑ Statement on a nonproprietory name adopted by the USAN council
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- ↑ Prous Science: Molecule of the Month November 2007[dead link]
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