Tofogliflozin

CHEMBL2105711 Phase 4 승인됨 Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
386.4 g/mol
LogP
1.5
Phase
4

Tofogliflozin is a highly selective sodium-glucose cotransporter 2 (SGLT2) inhibitor that blocks glucose reabsorption in the proximal renal tubule, promoting urinary glucose excretion (glucosuria) and lowering blood glucose in an insulin-independent manner. It is approved in Japan for type 2 diabetes and is under investigation for non-alcoholic fatty liver disease due to its effects on hepatic steatosis through caloric loss and indirect metabolic improvements. Its selectivity for SGLT2 over SGLT1 reduces the risk of GI adverse effects from intestinal glucose malabsorption.

분자량

386.4000 g/mol

LogP

1.50

TPSA

99.40 Ų

리핀스키 5의 법칙

통과

치료 영역

Pharmacokinetics (PK)

Pharmacodynamics (PD)

2D 구조

SVG PNG

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SMILES

CCc1ccc(Cc2ccc3c(c2)[C@]2(OC3)O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)cc1.O

InChI

InChI=1S/C22H26O6.H2O/c1-2-13-3-5-14(6-4-13)9-15-7-8-16-12-27-22(17(16)10-15)21(26)20(25)19(24)18(11-23)28-22;/h3-8,10,18-21,23-26H,2,9,11-12H2,1H3;1H2/t18-,19-,20+,21-,22+;/m1./s1

Molecular Formula

C22H26O6

HBD / HBA

4 / 6

회전 가능 결합

4

무거운 원자

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.

자주 묻는 질문

Tofogliflozin is a highly selective sodium-glucose cotransporter 2 (SGLT2) inhibitor that blocks glucose reabsorption in the proximal renal tubule, promoting urinary glucose excretion (glucosuria) and lowering blood glucose in an insulin-independent manner. It is approved in Japan for type 2 diabetes and is under investigation for non-alcoholic fatty liver disease due to its effects on hepatic steatosis through caloric loss and indirect metabolic improvements. Its selectivity for SGLT2 over SGLT1 reduces the risk of GI adverse effects from intestinal glucose …

Yes, Tofogliflozin is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.

{# References & Data Sources section for drug detail pages. Renders standard pharmacological database links plus the drug's data_sources field. #}

References & Data Sources

  • ChEMBL — European Bioinformatics Institute (EBI). CHEMBL2105711. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 46908929. Chemical information database.

Data aggregated from publicly available pharmacological databases. Last updated 2026-03-28.

의학적 면책조항

This content is for educational and informational purposes only. It is not a substitute for professional medical advice, diagnosis, or treatment. Always consult a qualified healthcare provider before making medication decisions.

Data sources: ChEMBL, PubChem, DailyMed.