| Weight | 126.119 g/mol |
|---|---|
| Formula | C4H6N4O |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 3 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
360-97-4 (360-97-4)
Aminoimidazole Carboxamide · Ba 2756
Score:
#1486 in Biochemistry
,
#3491 in Biology
,
#4368 in Chemistry
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- 5-aminoimidazole-4-carboxamide ribonucleoside. A specific method for activating AMP-activated protein kinase in intact cells? (FEBS Journal, 1995)
- 5Aminoimidazole4Carboxamide Ribonucleoside (FEBS Journal, 1995)
- Knockout of the 2 but Not 1 5-AMP-activated Protein Kinase Isoform Abolishes 5-Aminoimidazole-4-carboxamide-1--4-ribofuranosidebut Not Contraction-induced Glucose Uptake in Skeletal Muscle (Journal of Biological Chemistry, 2004)
- 5-aminoimidazole-4-carboxamide riboside mimics the effects of insulin on the expression of the 2 key gluconeogenic genes PEPCK and glucose-6-phosphatase. (Diabetes, 2000)
- 5-Aminoimidazole-4-carboxamide-1--D-ribofuranoside Inhibits Cancer Cell Proliferation in Vitro and in Vivo via AMP-activated Protein Kinase (Journal of Biological Chemistry, 2005)
- Cell Cycle Regulation via p53 Phosphorylation by a 5-AMP Activated Protein Kinase Activator, 5-Aminoimidazole- 4-Carboxamide-1--d-Ribofuranoside, in a Human Hepatocellular Carcinoma Cell Line (Biochemical and Biophysical Research Communications, 2001)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Aminoimidazole Carboxamide
- Ba 2756
-
SMILESC1=NC(=C(N1)C(=O)N)N
-
InChIKeyDVNYTAVYBRSTGK-UHFFFAOYSA-N
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