Miglitol

CHEMBL1561 Phase 4 Disetujui Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
207.2 g/mol
LogP
-2.6
Phase
4

This oral medication slows the digestion and absorption of carbohydrates in the intestine, helping to prevent blood sugar from rising too high after meals. It is used alongside diet and exercise to improve blood sugar control in type 2 diabetes.

Berat Molekul

207,2200 g/mol

LogP

-2,60

TPSA

104,00 Ų

Lipinski RO5

Lulus

Area Terapeutik

Mekanisme Kerja

Selectively blocks angiotensin II type 1 (AT1) receptors, preventing the vasoconstrictive and aldosterone-secreting effects of angiotensin II. This results in vasodilation, reduced sodium retention, and decreased blood pressure.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Mekanisme

Selectively blocks angiotensin II type 1 (AT1) receptors, preventing the vasoconstrictive and aldosterone-secreting effects of angiotensin II. This results in vasodilation, reduced sodium retention, and decreased blood pressure.

Struktur 2D

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SMILES

OCCN1C[C@H](O)[C@@H](O)[C@H](O)[C@H]1CO

InChI

InChI=1S/C8H17NO5/c10-2-1-9-3-6(12)8(14)7(13)5(9)4-11/h5-8,10-14H,1-4H2/t5-,6+,7-,8-/m1/s1

Molecular Formula

C8H17NO5

HBD / HBA

5 / 6

Ikatan yang Dapat Dirotasi

3

Atom Berat

14

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.

Pertanyaan yang Sering Diajukan

This oral medication slows the digestion and absorption of carbohydrates in the intestine, helping to prevent blood sugar from rising too high after meals. It is used alongside diet and exercise to improve blood sugar control in type 2 diabetes.

Selectively blocks angiotensin II type 1 (AT1) receptors, preventing the vasoconstrictive and aldosterone-secreting effects of angiotensin II. This results in vasodilation, reduced sodium retention, and decreased blood pressure.

Yes, Miglitol 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). CHEMBL1561. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 441314. Chemical information database.

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

Penyangkalan Medis

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.