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AICAR

  • Product NameAICAR
  • CasNo2627-69-2
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Quality products make an important contribution to long-term revenue and profitability. Factory supply AICAR 2627-69-2 with sufficient stock and high standard

1.What is the AICAR ?

Solid

ChEBI: A 1-ribosylimidazolecarboxamide in which the carboxamide group is situated at position 4 of the imidazole ring, which is further substituted at position 5 by an amino group. A purine nucleoside analogue and activator of AMP-activated protein kinase, it is is used for the treatment of acute lymphoblastic leukemia and is reported to have cardioprotective effects.

AICAR (2627-69-2) activates AMP-activated protein kinase (AMPK). Promotes ligand-independent activation of the insulin receptor.1 Promotes skeletal muscle autophagy via activation of FoxO3a.2 Controls smooth muscle cell hyperproliferation in vascular disease.3 ?Induces osteogenic differentiation in mesenchymal stem cells.4 Inhibits proinflammatory response in glial cells.5 Cell permeable.

2.What is the CAS number for AICAR ?

The CAS number of AICAR is 2627-69-2.

3.What are another words for AICAR ?

Synonyms for AICAR 2627-69-2:Imidazole-4-carboxamide,5-amino-1-b-D-ribofuranosyl- (6CI,7CI,8CI);1-Ribosyl-4-carboxamido-5-aminoimidazole;1-b-D-Ribofuranosyl-5-amino-4-imidazolecarboxamide;5-Amino-1-ribosyl-4-imidazolecarboxamide;5-Amino-1-b-D-ribofuranosylimidazole-4-carboxamide;5-Amino-4-imidazolecarboxamide ribofuranoside;5-Amino-4-imidazolecarboxamideriboside;5-Aminoimidazole-4-carboxamide 1-(b-D-ribofuranoside);AIC-Riboside;AICA-Riboside;Acadesine;Arasine;NSC 105823;GP 1-110;

4.What is AICAR (2627-69-2) used for?

5-Aminoimidazole-4-carboxamide 1-beta-D-ribofuranoside is used as a cell permeable activator of AMP-activated protein kinase (AMPK), a metabolic master regulator that is activated in times of reduced energy availability (high cellular AMP:ATP ratios) and serves to inhibit anabolic processes. In vivo, pharmacologic activation of AMPK with AICAR mimics exercise and triggers insulin-independent glucose uptake by skeletal muscle.

InChI:InChI=1/C9H14N4O5/c10-7-4(8(11)17)12-2-13(7)9-6(16)5(15)3(1-14)18-9/h2-3,5-6,9,14-16H,1,10H2,(H2,11,17)/t3-,5-,6-,9-/m1/s1

Relevant articles related to AICAR:

Article

Source

Interrogating the mechanism of a tight binding inhibitor of AIR carboxylase

Firestine, Steven M.,Wu, Weidong,Youn, Hasik,Jo Davisson

, p. 794 - 803 (2009)

Synthesis of N-1 and ribose modified inosine analogues on solid support

Oliviero, Giorgia,Amato, Jussara,Borbone, Nicola,D'Errico, Stefano,Piccialli, Gennaro,Mayol, Luciano

, p. 397 - 400 (2007)

SAICAR Synthesis method

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Paragraph 0053; 0061-0062; 0076; 0083-0084; 0098; 0105-0106, (2021/11/06)

5.Buy AICAR with the best price .

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