| Weight | 295.188 g/mol |
|---|---|
| Formula | C8H14N3O7P |
| Hydrogen Acceptors | 8 |
| Hydrogen Donors | 5 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 4 |
Aminoimidazole ribotide (25635-88-5)
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- Inhibition of 5-aminoimidazole-4-carboxamide ribotide transformylase, adenosine deaminase and 5-adenylate deaminase by polyglutamates of methotrexate and oxidized folates and by 5-aminoimidazole-4-carboxamide riboside and ribotide (Biochemical Journal, 1986)
- Biosynthesis of Thiamin : 5-Aminoimidazole Ribotide as the Precursor of All the Carbon Atoms of the Pyrimidine Moiety (Journal of the American Chemical Society, 1984)
- Conversion of 5-aminoimidazole ribotide to the pyrimidine of thiamin in enterobacteria : study of the pathway with specifically labeled samples of riboside (Biochimica et Biophysica Acta, 1990)
- Relationship between 5-aminoimidazole-4-carboxamide-ribotide and AMP-activated protein kinase activity in the perfused mouse heart (American Journal of Physiology-heart and Circulatory Physiology, 2006)
- 5-Aminoimidazole-4-carboxamide Ribotide Transformylase-IMP Cyclohydrolase from Human CCRF-CEM Leukemia Cells: Purification, pH Dependence, and Inhibitors? (Biochemistry, 1994)
- Inhibition of fructose-1,6-bisphosphatase by aminoimidazole carboxamide ribotide prevents growth of Salmonella enterica purH mutants on glycerol (Journal of Biological Chemistry, 2006)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=C(N(C=N1)C2C(C(C(O2)COP(=O)(O)O)O)O)N
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InChIKeyPDACUKOKVHBVHJ-UHFFFAOYSA-N
- Pubchem - Aminoimidazole ribotide
- Wikipedia - 5-Aminoimidazole ribotide
5'-Phosphoribosyl-5-aminoimidazole (or aminoimidazole ribotide) is an intermediate in the formation of purines. Thus, it is an intermediate in the adenine pathway, and is synthesized from 5'-phosphoribosylformylglycinamidine by AIR synthetase.
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