Buformin

CHEMBL39736 Phase 4 Onaylandı Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
157.2 g/mol
LogP
-0.6
Phase
4

An older biguanide antidiabetic drug related to metformin, used to treat type 2 diabetes before being withdrawn from most markets due to an unacceptably high risk of lactic acidosis. It lowered blood sugar by reducing glucose production in the liver and improving insulin sensitivity. It is largely of historical interest in the development of diabetes pharmacology.

Moleküler Ağırlık

157,2200 g/mol

LogP

-0,60

TPSA

103,00 Ų

Lipinski RO5

Geçer

Terapötik Alanlar

Etki Mekanizması

Decreases hepatic glucose production, increases insulin sensitivity in peripheral tissues, and reduces intestinal absorption of glucose. The primary mechanism involves activation of AMP-activated protein kinase (AMPK) in hepatocytes.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Mekanizma

Decreases hepatic glucose production, increases insulin sensitivity in peripheral tissues, and reduces intestinal absorption of glucose. The primary mechanism involves activation of AMP-activated protein kinase (AMPK) in hepatocytes.

2D Yapı

SVG PNG

Cite this structure


                        

Embed this structure


                        

SMILES

CCCCNC(=N)NC(=N)N

InChI

InChI=1S/C6H15N5/c1-2-3-4-10-6(9)11-5(7)8/h2-4H2,1H3,(H6,7,8,9,10,11)

Molecular Formula

C6H15N5

HBD / HBA

3 / 1

Döndürülebilir Bağlar

4

Ağır Atomlar

11

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.

Sıkça Sorulan Sorular

An older biguanide antidiabetic drug related to metformin, used to treat type 2 diabetes before being withdrawn from most markets due to an unacceptably high risk of lactic acidosis. It lowered blood sugar by reducing glucose production in the liver and improving insulin sensitivity. It is largely of historical interest in the development of diabetes pharmacology.

Decreases hepatic glucose production, increases insulin sensitivity in peripheral tissues, and reduces intestinal absorption of glucose. The primary mechanism involves activation of AMP-activated protein kinase (AMPK) in hepatocytes.

Yes, Buformin 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). CHEMBL39736. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 2468. Chemical information database.

Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.

Tıbbi Sorumluluk Reddi

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.