2627-69-2 Usage
adenosine regulating agents
Acadesine is the prototype of a new class of compounds termed adenosine regulating agents. Acadesine is a purine nucleosid analogue that enters the myocyte and is immediately phosphorylated to ZMP (AICA ribotide), which is further metabolised to Inosine mono-phosphate (an intermediate in the synthesis ofadenosine triphosphate (ATP) and guanosine triphos-phate). Claims that acadesine may serve as a substrate for ATP synthesis and result in repletion of myocardial ATP were supported by some studies and refuted by others. Because acadesine may be a precursor in the synthesis of myocardial ATP it was proposed as a possible agent of myocardial protection during ischaemia, particularly because myocardial ATP depletion has been linked to cell death.
Description
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.
Chemical Properties
Solid
Originator
AICA,BIOMOL
Uses
Different sources of media describe the Uses of 2627-69-2 differently. You can refer to the following data:
1. glucose uptake stimulant; AMPK activator
2. AICAR is a nucleoside analogue that is able to enter nucleoside pools and is able to significantly increase levels of adenosine during periods of ATP breakdown. Adenosine-regulating agents (ARAs) hav
e been recognized for therapeutic potential in myocardial ischemia. Cardioprotective.
3. 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.
Definition
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.
Manufacturing Process
Adenosine 3', 5'-cyclic phosphate N'-oxide (76.0 g, 0.200 mole) as the dihydrate was dissolved in a solution of 400 ml DMSO and 31.0 g (0.204
mole) 1,5-diazabicyclo[5.4.0]undec-5-ene. The solution was cooled to 15°C
and 40 ml methyl iodide was added with stirring at room temperature. After
30 min, the mixture had gelled; 1.5 L ethanol was added and the solid was
thoroughly homogenized by vigorous stirring. The solid was filtered, and the
resulting paste was resuspended in 2 L ethanol and homogenized. The product
was again filtered, washed with ethanol and ether, and dried, giving 80.4 g of
1-methoxyadenosine 3',5'-cyclic phosphate suitable for further transformation
(recrystallization from aqueous methanol with ether).
A solution of 30.0 g 1-methoxyadenosine 3',5'-cyclic phosphate (81.5 mmole),
20.0 g NaHCO3 (238 mmole), and 300 ml H2O was refluxed 45 mm. The pH
of the solution was adjusted to 2.5 with Dowex 50x8 (H)+ while warm, and a
water pump vacuum was applied to mixture to remove CO2. The pH was
readjusted to 9-10 with NaOH, and the resin was removed by filtration. The
solution was passed onto a column containing 400 ml Dowex 1x2 (formate,
100-200 mesh), and the column was washed well with water. The column was
eluted with a gradient of 4 L water in the mixing chamber and 4 L 4 N formic
acid in the reservoir. The first major product, coming after about 2 L eluate,
was 5-amino-N-methoxy-1-β-D-ribofuranosylimidazole-4-carboxamidine 3',5'-
cyclic phosphate, giving 5.4 g (19%) after evaporation of the solvent and
trituration of the residue with ethanol (recrystallization from water).
A solution of 5.0 g (14.3 mmoles) 5-amino-N-methoxy-1-β-Dribofuranosylimidazole-
4-carboxamidine 3',5'-cyclic phosphate in 200 ml H2
preheated to 60°C and containing approximately 5.0 g moist sponge nickel
catalyst, was shaken with 2-3 atm. H2 at 60°C for 2 h. The filtered solution
was evaporated to dryness to give 3.75 g of 5-amino-1-β-Dribofuranosylimidazole-
4-carboxamidine 3',5'-cyclic phosphate (82%),
(recrystallization from water).
A mixture of 4.0 g (12.5 mmole) 5-amino-1-β-D-ribofuranosylimidazole-4-
carboxamidine 3',5'-cyclic phosphate and 100 ml conc. NH4OH was heated in
a bomb at 100°C for 16 h, then cooled and evaporated in vacuum. The
residue was taken up in 100 ml H2O and applied to a 2.5x20 cm column of
Dowex 1x2 (formate form, 100-200 mesh). After washing well with H2O the
column was eluted with a gradient of 1 L H2O in the mixing chamber and 1 L
3 N formic acid in the reservoir. Fractions containing the product, appearing
near the end of the elution, were evaporated. Trituration of the residue with
EtOH gave 2.90 g (68%) of 5-amino-1-β-D-ribofuranosylimidazole-4-
carboxamide 3',5'-cyclic phosphate.
The 5-amino-1-β-D-ribofuranosylimidazole-4-carboxamide may be produced
by hydrolysis of 5-amino-1-β-D-ribofuranosylimidazole-4-carboxamide 3',5'-
cyclic phosphate with NaOH.
Therapeutic Function
Cardiotonic, Platelet aggregation inhibitor
General Description
Adenosine monophosphate?protein kinase (AMPK) activator 5-aminoimidazole-4-carboxamide?ribonucleotide?(AICAR)?modulates cellular energy. It regulates lipid and glucose metabolism, pro-inflammatory responses,?cytokine production,?cell proliferation and apoptosis. AICAR improves ischemia or reperfusion injury and kidney fibrosis in rats. It provides protection against acute tubular necrosis.
Biological Activity
Cell-permeable, allosteric activator of AMP-activated protein kinase (AMPK). Augments proliferation, differentiation and mineralization of osteoblastic MC3T3-EI cells and attenuates psychosine-induced expression of proinflammatory cytokines and iNOS in astrocytes.
Biochem/physiol Actions
AICAR is 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.
References
1) Chopra et al. (2012), Phosphorylation of the insulin receptor by AMP-activated protein kinase (AMPK) promotes ligand-independent activation of the insulin signalling pathway in rodent muscle; Diabetologia, 55 783
2) Sanchez et al. (2012), AMPK promotes skeletal muscle autophagy through activation of forkhead FoxO3a and interaction with Ulk1; J. Cell Biochem., 113 695
3) Ferri et al. (2012), AMP-activated protein kinase and the control of smooth muscle cell hyperproliferation in vascular disease; Vascul. Pharmacol., 56 9
4) Wu et al. (2011) AICAR, a small chemical molecule, primes osteogenic differentiation of adult mesenchymal stem cells; Int. J. Artif. Organs, 34 1128
5) Giri et al. (2004) 5-aminoimidazole-4-carboxamide-1-beta-4-ribofuranoside inhibits proinflammatory response in glial cells: a possible role of AMP-activated protein kinase; J. Neurosci., 24 479
Check Digit Verification of cas no
The CAS Registry Mumber 2627-69-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,2 and 7 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2627-69:
(6*2)+(5*6)+(4*2)+(3*7)+(2*6)+(1*9)=92
92 % 10 = 2
So 2627-69-2 is a valid CAS Registry Number.
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
2627-69-2Relevant articles and documents
Interrogating the mechanism of a tight binding inhibitor of AIR carboxylase
Firestine, Steven M.,Wu, Weidong,Youn, Hasik,Jo Davisson
, p. 794 - 803 (2009)
The enzyme aminoimidazole ribonucleotide (AIR) carboxylase catalyzes the synthesis of the purine intermediate, 4-carboxy-5-aminoimidazole ribonucleotide (CAIR). Previously, we have shown that the compound 4-nitro-5-aminoimidazole ribonucleotide (NAIR) is
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)
Herein, we report the synthesis and the use of new N-1-dinitrophenyl-inosine based solid supports, in which the C-2 of the purine base is strongly activated toward the attack of N-nucleophiles. The synthesized supports, binding the nucleoside by a 5′-O-monomethoxytrityl function, have been used to accomplish the synthesis of a small library of N-1 alkylated inosine and AICAR derivatives. In addition, cleavage of the 2′-3′ ribose bond of N-1 alkylated inosine derivatives anchored to the supports allowed to prepare a new set of N-1 alkylated-2′,3′-secoinosine derivatives in high yields.
IMPROVEMENTS TO ANALOGOUS COMPOUNDS OF 6-THIOGUANOSINE TRIPHOSPHATE, THEIR USE IN MEDICAL FIELDS AND PROCESSES FOR THEIR PREPARATION
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Page/Page column 65, (2008/06/13)
The invention relates to analogous compounds of 6-thioguanosine triphosphate of general formula (I). A compound of the general formula (I); wherein the dashed bond in the sugar moiety can be either single or double and wherein R1 , R2, R3, R4 or R5, equal or different between each other, have general formula -(Int)m-Ter, wherein m is between 0 and 12 and lnt and Ter are Internal and Terminal building blocks, wherein lnt is selected from the group consisting of formula (II); and Ter is selected from the group consisting of formula (III). And wherein X represents either carbon or nitrogen atom within aromatic ring, Y represents either oxygen or sulphur atom and an additional group Q, group Qi or groups Qi (Qi indicates that the group or several groups may be bound to any unsaturated moiety of the ring) are selected from the group consisting of -OH, -COOH, -N(CH3)2, -N(CH2-CH3)2| -CO-CH3, -CO-O-CH3, -O-CH3, -S-CH3,-SO2-CH3, -CN, -NO2 or -Halogen elements, and wherein R5 may be formula (IV) and metal and ammonium salts thereof, wherein n is between O and 5, or oxygen or phosphorus is partially or completely replaced by nitrogen, sulphur, methyleno groups or their derivatives. The invention also concerns the uses of the above mentioned compounds in medical field and the process for their preparation.
