360-97-4
360-97-4
Chemical Structure
5-Amino-3H-imidazole-4-Carboxamide
Synonym(s): 5-Aminoimidazole-4-carboxamide; AICA
- CAS No.: 360-97-4
- Formula:C4H6N4O
- Molecular Weight:126.12
IUPAC Name: 5-amino-1H-imidazole-4-carboxamide
InChIKey: DVNYTAVYBRSTGK-UHFFFAOYSA-N
SMILES: O=C(C1=C(N)NC=N1)N
Biological Activity: 5-Amino-3H-imidazole-4-Carboxamide (5-Aminoimidazole-4-carboxamide; AICA) is an important precursor for the synthesis of purines in general and of the nucleobases adenine and guanine in particular[1][2][3].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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5-Amino-3H-imidazole-4-Carboxamide | 99.99% | 5-Amino-3H-imidazole-4-Carboxamide (5-Aminoimidazole-4-carboxamide; AICA) is an important precursor for the synthesis of purines in general and of the nucleobases adenine and guanine in particular. | ||||||||||||||||||||
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5-Amino-3H-imidazole-4-Carboxamide (Standard) | ≥98% | 5-Amino-3H-imidazole-4-Carboxamide (Standard) is the analytical standard of 5-Amino-3H-imidazole-4-Carboxamide. This product is intended for research and analytical applications. 5-Amino-3H-imidazole-4-Carboxamide (AICA) is an important precursor for the synthesis of purines in general and of the nucleobases adenine and guanine in particular. | ||||||||||||||||||||
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References
- [1]. YANG LIU. VARIABLE-TEMPERATURE 1 H-NMR AND AB INITIO STUDY OF 5-AMINO-IMIDAZOLE-4-CARBOXAMIDE (AICA): COMPETING PATHS FOR AMIDE-H SCRAMBLING. DECEMBER 2008.
- [2]. Wojtaszewski JF, et al. Glycogen-dependent effects of 5-aminoimidazole-4-carboxamide (AICA)-riboside on AMP-activated protein kinase and glycogen synthase activities in rat skeletal muscle. Diabetes. 2002 Feb;51(2):284-92. [Content Brief]
- [3]. Sheldrick W S, et al. The structures of two tricyclic phosphoranes displaying facial placement of the fused bicyclic system[J]. Acta Crystallographica Section B: Structural Crystallography and Crystal Chemistry, 1980, 36(10): 2316-2323.
