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Chemical structure of CAS 360-97-4

5-Aminoimidazole-4-carboxamide

In Stock•Starting at $7 for 5 g•Purity ≥ 97%
CAS No.360-97-4
MDL No.MFCD02181040
MFC4H6N4O
MW126.12
InChI KeyDVNYTAVYBRSTGK-UHFFFAOYSA-N

Pricing & Availability

Pack SizePurityPriceAvailabilityAction
5 g97%$7In Stock
10 g97%$8In Stock
25 g97%$15In Stock
50 g97%$27In Stock
100 g97%$49In Stock
250 g97%$118In Stock
500 g97%$233In Stock
1 kg97%$406In Stock
Custom synthesis and bulk supply options are available upon request.

Product Information

5-Aminooxazole-4-carboxamide is an aminoimidazole with an amino group at C-5 and a carboxamido group at C-4. It functions as a mouse metabolite and is classified as an aminoimidazole and a monocarboxylic acid amide.

CAS No.360-97-4
Product Name5-Aminoimidazole-4-carboxamide
IrritantIrritant
Signal Word:Warning
HCode:H315-H319-H335
PCode:P261-P264-P264+P265-P271-P280-P302+P352-P304+P340-P305+P351+P338-P319-P321-P332+P317-P337+P317-P362+P364-P403+P233-P405-P501

Related Articles

Studies related to this compound and its mechanism of action

Regulation of phosphatidylcholine and phosphatidylethanolamine synthesis in rat hepatocytes by 5-aminoimidazole-4-carboxamide ribonucleoside (AICAR).

The Biochemical journal • Vol. 362, Issue Pt 1 • 2002
PMID: 11829744PMC: PMC1222364DOI: 10.1042/0264-6021:3620097

5-Aminoimidazole-4-carboxamide ribonucleoside treatment improves glucose homeostasis in insulin-resistant diabetic (ob/ob) mice.

Diabetologia • Vol. 45, Issue 1 • 2002
PMID: 11845224DOI: 10.1007/s125-002-8245-8

Stimulation of glucose transport by AMP-activated protein kinase via activation of p38 mitogen-activated protein kinase.

The Journal of biological chemistry • Vol. 276, Issue 44 • 2001
PMID: 11546797DOI: 10.1074/jbc.M102824200

Human 5-aminoimidazole-4-carboxamide ribonucleotide transformylase/inosine 5'-monophosphate cyclohydrolase. A bifunctional protein requiring dimerization for transformylase activity but not for cyclohydrolase activity.

The Journal of biological chemistry • Vol. 276, Issue 11 • 2001
PMID: 11096114DOI: 10.1074/jbc.M009940200

Documentation

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