Metformin
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Metformin
structure -
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CAS No:
657-24-9
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Formula:
C4H11N5
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Chemical Name:
Metformin
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Synonyms:
Imidodicarbonimidic diamide,N,N-dimethyl-;Biguanide,1,1-dimethyl-;N,N-Dimethylimidodicarbonimidic diamide;N,N-Dimethylbiguanide;N1,N1-Dimethylbiguanide;1,1-Dimethylbiguanide;N,N-Dimethyldiguanide;Flumamine;Metformin;NNDG;Dimethylbiguanide;DMGG;Fluamine;Gliguanid;Haurymelin;Metiguanide;Siofor;N′-Dimethylguanylguanidine;Metphage;Ficonax;Emiphage;Cidophage;Glucofine;Glifor;1-[Amino(dimethylamino)methylidene]guanidine;1-Carbamimidamido-N,N-dimethylmethanimidamide;[[Amino(dimethylamino)methylidene]amino]methanimidamide;Okamet
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Categories:
Active Pharmaceutical Ingredients > Hormones and the Endocrine System
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CAS No:
Description
Metformin (1,1-Dimethylbiguanide) inhibits the mitochondrial respiratory chain in the liver, leading to activation of AMPK, enhancing insulin sensitivity for type 2 diabetes research. Metformin can cross the blood-brain barrier and triggers autophagy[1].
Characteristics
91.5
-1.3
Solid
1.3±0.1 g/cm3
199-200 °C
224.1ºC at 760 mmHg
58.1±22.6 °C
1.576
Freely soluble as HCl salt
Keep container tightly closed in a dry and well-ventilated place. Recommended storage temperature 2 - 8 deg C. Storage class (TRGS 510): Non Combustible Solids. /Metformin hydrochloride/
7.58X10-5 mm Hg at 25 deg C (est)
LD50 oral in mouse: 1450mg/kg
12.4None
Safety Information
Stable under recommended storage conditions. /Metformin hydrochloride/
P264, P270, P301+P312, P330, P501
H302
Computed Properties
Molecular Weight:129.16
XLogP3:-1.3
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:129.10144537
Monoisotopic Mass:129.10144537
Topological Polar Surface Area:91.5
Heavy Atom Count:9
Complexity:132
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
Drug Function and Efficacy
Improve glucose tolerance in patients with type 2 diabetes, lower basal and postprandial blood sugar; reduce liver glucose production, reduce intestinal glucose absorption, and improve insulin sensitivity by increasing peripheral blood glucose absorption and utilization.
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