5-Amino-4-imidazolecarboxamide
5-Amino-4-imidazolecarboxamide (CAS No.: 360-97-4) is an imidazole-derived intermediate in purine biosynthesis that functions as a key precursor in the intracellular formation of nucleobases such as adenine and guanine, thereby playing an essential role in cellular nucleotide metabolism and proliferation-related processes. As a metabolite associated with certain antineoplastic agent pathways, it is also recognized for its utility as a condensation intermediate in the preparation of nucleosides and nucleotides, supporting its relevance in synthetic and biochemical studies. This compound is closely related to the biologically active ribonucleoside derivative AICAR, which is widely used to investigate AMP-activated protein kinase signaling and associated metabolic regulatory networks, positioning 5-amino-4-imidazolecarboxamide as a valuable upstream tool for probing purine metabolism and energy-sensing pathways. Although direct bioactivity data for this compound are limited, its functional analogs and derivatives exhibit activity in the nanomolar to micromolar range in enzyme modulation and pathway studies, providing a contextual framework for its experimental use. In research settings, it is commonly employed in studies of metabolic flux, nucleotide biosynthesis, and signal transduction, including applications in cell-based assays and biochemical pathway reconstitution, where concentrations are selected based on specific experimental design and objectives.
| Physical Appearance | Solid |
| Storage | -20°C |
| M.Wt | 126.12 |
| Cas No. | 360-97-4 |
| Formula | C4H6N4O |
| Solubility | ≥10.13 mg/mL in EtOH; ≥10.3 mg/mL in H2O; ≥52.4 mg/mL in DMSO |
| Chemical Name | 5-amino-1H-imidazole-4-carboxamide |
| Canonical SMILES | NC1=C(C(N)=O)N=CN1 |
| Shipping Condition | Small Molecules with Blue Ice, Modified Nucleotides with Dry Ice. |
| General tips | We do not recommend long-term storage for the solution, please use it up soon. |







