CAS 21299-72-9
:4-aminoimidazol-5-carboxamida
- 1H-Imidazole-4-carboxamide, 5-amino-
- 5-Amino-4-Imidazolylcarboxamide
- 5-Amino-3H-Imidazole-4-Carboxamide
- 5-Amino-4-Imidazolecarboxamide
- 5-Aminoimidazole-4-Carboxamide
- 4(5)-Amino-5(4)-Imidazolecarboxamide
- 4-Amino-5-Imidazolecarboxamid
- 5-Amino-1H-Imidazole-4-Carboxamid
- 5-Amino-4-glyoxalinecarboxamide
- 5-Amino-Imidazole-4-Carboxamid
- Aic Aminoimidazolecarboxamide
- Ba2756 Diazol-C
- 1H-Imidazole-4-carboxamide, 5-amino- 5-amino-4-imidazolylcarboxamide
- 4-Amino-5-imidazolecarboxamide monohydrate
- AICA, 4-Amino-5-carbamoylimidazole
- 4-Amino-5-imodazole
- 4-Amino-5-imidazole carboxamide
- 4-(1-Aminovinyl)-1H-imidazol-5-amine
- Aica
- 4-Amino-5-imidazolecarboxamide
- 1H-imidazole-5-carboxamide, 4-amino-
- 4-Amino-1H-imidazole-5-carboxamide
- 5-Amino-1H-imidazole-4-carboxamide
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5-Amino-4-imidazolecarboxamide
CAS:5-Amino-4-imidazolecarboxamide is an imidazole derivative.Fórmula:C4H6N4OPureza:99.17%Forma y color:SolidPeso molecular:126.125-Amino-4-imidazolecarboxamide
CAS:5-Amino-4-imidazolecarboxamidePureza:≥98%Peso molecular:126.12g/mol5-Aminoimidazole-4-carboxamide HCl
CAS:5-Aminoimidazole-4-carboxamide HCl (5-AICA) is a compound that is used for the treatment of bowel disease. It inhibits the synthesis of 5'-nucleotidase and phosphoribosyl transferase, which are enzymes responsible for the conversion of nucleotide monophosphates to nucleotide diphosphates. This inhibition leads to a decrease in the amount of adenosine triphosphate (ATP) produced by cells, which may be due to its ability to inhibit ATP synthase activity. 5-AICA also has been shown to bind to DNA and inhibit transcriptional activities. The binding of 5-AICA may be due to its ability to form hydrogen bonds with guanine residues in DNA or its capability to form covalent bonds with thymidine residues in DNA. 5-AICA also has been shown to have cytotoxic effects on HL60 cells, as well as other
Pureza:Min. 95%Forma y color:PowderPeso molecular:126.12 g/mol




