Sotagliflozin
Sotagliflozin is a dual sodium-glucose cotransporter 1 and 2 (SGLT1/SGLT2) inhibitor used for the reduction of cardiovascular death, hospitalization for heart failure, and urgent heart failure visits in adults with heart failure and type 2 diabetes with chronic kidney disease. By inhibiting both intestinal SGLT1 and renal SGLT2, it reduces glucose absorption and renal glucose reabsorption, lowers blood glucose, and reduces sodium retention with accompanying reductions in heart failure risk. Its dual mechanism provides complementary glycosuric and cardiorenal benefits.
الوزن الجزيئي
424,9000 g/mol
LogP
3,20
TPSA
104,00 Ų
قاعدة ليبينسكي للخمسة
ناجح
المجالات العلاجية
Pharmacokinetics (PK)
Pharmacodynamics (PD)
البنية ثنائية الأبعاد
Cite this structure
Embed this structure
SMILES
CCOc1ccc(Cc2cc([C@@H]3O[C@H](SC)[C@@H](O)[C@H](O)[C@H]3O)ccc2Cl)cc1
InChI
InChI=1S/C21H25ClO5S/c1-3-26-15-7-4-12(5-8-15)10-14-11-13(6-9-16(14)22)20-18(24)17(23)19(25)21(27-20)28-2/h4-9,11,17-21,23-25H,3,10H2,1-2H3/t17-,18-,19+,20+,21-/m1/s1
Molecular Formula
C21H25ClO5S
HBD / HBA
3 / 6
الروابط القابلة للدوران
6
الذرات الثقيلة
28
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.
الأسئلة الشائعة
Sotagliflozin is a dual sodium-glucose cotransporter 1 and 2 (SGLT1/SGLT2) inhibitor used for the reduction of cardiovascular death, hospitalization for heart failure, and urgent heart failure visits in adults with heart failure and type 2 diabetes with chronic kidney disease. By inhibiting both intestinal SGLT1 and renal SGLT2, it reduces glucose absorption and renal glucose reabsorption, lowers blood glucose, and reduces sodium retention with accompanying reductions in heart failure risk. Its dual mechanism provides complementary glycosuric and cardiorenal benefits.
Yes, Sotagliflozin 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). CHEMBL3039507. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 24831714. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-28.
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