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Aicar

  • CasNo: 2627-69-2
  • Purity:
  • Appearance: tan powder

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1.What is the AICAR ?

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.

9-((2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-1-((2-methoxyethoxy)methyl)-1,9-dihydro-6H-purin-6-one
659746-61-9

9-((2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-1-((2-methoxyethoxy)methyl)-1,9-dihydro-6H-purin-6-one

AICA riboside
2627-69-2

AICA riboside

Conditions
Conditions Yield
With sodium hydroxide; for 1h; Reflux;
74%
With sodium hydroxide; for 1h; Heating;
73%
9-((2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-1-((2-methoxyethoxy)methyl)-1,9-dihydro-6H-purin-6-one; With sodium hydroxide; water; for 1h; Heating / reflux;
With hydrogenchloride; In water; at 20 ℃;
70%
5-azido-1-β-D-ribofuranosyl-1H-imidazole-4-carboxamide
129878-03-1

5-azido-1-β-D-ribofuranosyl-1H-imidazole-4-carboxamide

AICA riboside
2627-69-2

AICA riboside

Conditions
Conditions Yield
With hydrogen; palladium on activated charcoal; In acetic acid; for 1.5h; under 760 Torr; Ambient temperature;
42%
With hydrogen; palladium on activated charcoal; In water; acetic acid; at 23 ℃; for 1h; under 760 Torr;
42%

2.What is the CAS number for AICAR ?

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

More information of AICAR 2627-69-2 are:

CAS Number

2627-69-2

Density

2.06 g/cm3

Melting Point

214-215 °C

Boiling Point

726.3 °C at 760 mmHg

Flash Point

393.1 °C

Vapor Pressure

3.83E-22mmHg at 25°C

Refractive Index

1.821

HS CODE

29349990

PSA

156.85000

LogP

-1.54280

Pka

13.27±0.70(Predicted)

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 the molecular formula of AICAR?

The chemical formula of  AICAR is C9H14N4O5 which containing 9 Carbon atoms,14 Hydrogen atoms,4 Nitrogen atoms and 5 Oxygen atoms,and the molecular weight of  AICAR is 258.234.

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

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.

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

Solid phase synthesis of nucleobase and ribose modified inosine nucleoside analogues

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

, p. 1649 - 1652 (2007)

SAICAR Synthesis method

-

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

6.Buy AICAR with the best price .

Xi'an Youbo Hui Biotechnology Co., Ltd. is a quality supplier of AICAR. Our main goal is customer satisfaction. Contact us to negotiate the best price for your business on AICAR 2627-69-2.

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