Voglibose

CHEMBL476960 Phase 4 ได้รับการอนุมัติ Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
267.3 g/mol
LogP
-4.1
Phase
4

Voglibose is an alpha-glucosidase inhibitor that competitively blocks intestinal alpha-glucosidase enzymes (maltase, sucrase, glucoamylase) on the brush border of the small intestine, delaying the digestion of complex carbohydrates and disaccharides and reducing postprandial glucose absorption. It is used primarily in Asian countries for type 2 diabetes mellitus management to reduce postprandial hyperglycemia with minimal risk of hypoglycemia. Its selective action on intestinal alpha-glucosidases results in localized effects with limited systemic absorption.

น้ำหนักโมเลกุล

267.2800 g/mol

LogP

-4.10

TPSA

154.00 Ų

Lipinski RO5

ผ่าน

ด้านการรักษา

Pharmacokinetics (PK)

Pharmacodynamics (PD)

โครงสร้าง 2 มิติ

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SMILES

OCC(CO)N[C@H]1C[C@](O)(CO)[C@@H](O)[C@H](O)[C@H]1O

InChI

InChI=1S/C10H21NO7/c12-2-5(3-13)11-6-1-10(18,4-14)9(17)8(16)7(6)15/h5-9,11-18H,1-4H2/t6-,7-,8+,9-,10-/m0/s1

Molecular Formula

C10H21NO7

HBD / HBA

8 / 8

พันธะที่หมุนได้

5

อะตอมหนัก

18

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.

คำถามที่พบบ่อย

Voglibose is an alpha-glucosidase inhibitor that competitively blocks intestinal alpha-glucosidase enzymes (maltase, sucrase, glucoamylase) on the brush border of the small intestine, delaying the digestion of complex carbohydrates and disaccharides and reducing postprandial glucose absorption. It is used primarily in Asian countries for type 2 diabetes mellitus management to reduce postprandial hyperglycemia with minimal risk of hypoglycemia. Its selective action on intestinal alpha-glucosidases results in localized effects with limited systemic absorption.

Yes, Voglibose 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). CHEMBL476960. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 444020. Chemical information database.

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

ข้อจำกัดความรับผิดชอบทางการแพทย์

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.