Ertugliflozin Pidolate
The pidolate salt form of ertugliflozin, this SGLT2 inhibitor lowers blood sugar by promoting glucose excretion through the kidneys. The salt form is used in the standard oral tablet formulation.
Masse moléculaire
566,0000 g/mol
TPSA
175,00 Ų
Mécanisme d'action
Selectively inhibits sodium-glucose cotransporter 2 (SGLT2) in the proximal renal tubule, reducing glucose reabsorption and promoting urinary glucose excretion. This lowers blood glucose levels independently of insulin secretion.
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Selectively inhibits sodium-glucose cotransporter 2 (SGLT2) in the proximal renal tubule, reducing glucose reabsorption and promoting urinary glucose excretion. This lowers blood glucose levels independently of insulin secretion.
Structure 2D
Cite this structure
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SMILES
CCOc1ccc(Cc2cc([C@]34OC[C@](CO)(O3)[C@@H](O)[C@H](O)[C@H]4O)ccc2Cl)cc1.O=C1CC[C@@H](C(=O)O)N1
InChI
InChI=1S/C22H25ClO7.C5H7NO3/c1-2-28-16-6-3-13(4-7-16)9-14-10-15(5-8-17(14)23)22-20(27)18(25)19(26)21(11-24,30-22)12-29-22;7-4-2-1-3(6-4)5(8)9/h3-8,10,18-20,24-27H,2,9,11-12H2,1H3;3H,1-2H2,(H,6,7)(H,8,9)/t18-,19-,20+,21-,22-;3-/m00/s1
Molecular Formula
C27H32ClNO10
HBD / HBA
6 / 10
Liaisons Rotatives
7
Atomes Lourds
39
No targets recorded
Target interaction data is not yet available for this drug.
No interactions recorded
Drug interaction data is not yet available for this compound.
No side effects recorded
Side effect data is not yet available for this drug.
Foire aux questions
The pidolate salt form of ertugliflozin, this SGLT2 inhibitor lowers blood sugar by promoting glucose excretion through the kidneys. The salt form is used in the standard oral tablet formulation.
Selectively inhibits sodium-glucose cotransporter 2 (SGLT2) in the proximal renal tubule, reducing glucose reabsorption and promoting urinary glucose excretion. This lowers blood glucose levels independently of insulin secretion.
Yes, Ertugliflozin Pidolate is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.
References & Data Sources
- ChEMBL — European Bioinformatics Institute (EBI). CHEMBL5315054. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 57339449. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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