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ADENOSINE, PERIODATE OXIDIZED

Product Name
ADENOSINE, PERIODATE OXIDIZED
CAS No.
34240-05-6
Chemical Name
ADENOSINE, PERIODATE OXIDIZED
Synonyms
AdenosineDialdehyde(ADOX);ADENOSINE-2',3'-DIALDEHYDE;periodate-oxidizedadenosine;ADENOSINE, PERIODATE OXIDIZED;Adenosine, periodate oxidized >=93%;2-(1-(6-aMino-9H-purin-9-yl)-2-oxoethoxy)-3-hydroxypropanal;Hydracrylaldehyde, 2-((6-amino-9H-purin-9-yl)formylmethoxy)-;9H-Purine-9-acetaldehyde, 6-amino-α-(1-formyl-2-hydroxyethoxy)-;6-amino-alpha-(1-formyl-2-hydroxyethoxy)-9h-purine-9-acetaldehyd;alpha-(Hydroxymethyl)-alpha'-(6-aminopurin-9-yl)diglycolaldehyde
CBNumber
CB1348648
Molecular Formula
C10H11N5O4
Formula Weight
265.23
MOL File
34240-05-6.mol
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ADENOSINE, PERIODATE OXIDIZED Property

Boiling point:
532.9±60.0 °C(Predicted)
Density 
1.69±0.1 g/cm3(Predicted)
storage temp. 
-20°C
solubility 
Soluble in DMSO
form 
powder
pka
13.72±0.10(Predicted)
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Safety

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
1
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H370Causes damage to organs

Precautionary statements

P260Do not breathe dust/fume/gas/mist/vapours/spray.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P270Do not eat, drink or smoke when using this product.

P307+P311IF exposed: call a POISON CENTER or doctor/physician.

P321Specific treatment (see … on this label).

P405Store locked up.

P501Dispose of contents/container to..…

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
A7154
Product name
Adenosine, periodate oxidized
Purity
≥93%
Packaging
25mg
Price
$121
Updated
2024/03/01
Sigma-Aldrich
Product number
A7154
Product name
Adenosine, periodate oxidized
Purity
≥93%
Packaging
100mg
Price
$376
Updated
2024/03/01
Cayman Chemical
Product number
15644
Product name
Adenosine Dialdehyde
Purity
≥95%
Packaging
5mg
Price
$31
Updated
2024/03/01
Cayman Chemical
Product number
15644
Product name
Adenosine Dialdehyde
Purity
≥95%
Packaging
10mg
Price
$48
Updated
2024/03/01
Cayman Chemical
Product number
15644
Product name
Adenosine Dialdehyde
Purity
≥95%
Packaging
25mg
Price
$89
Updated
2024/03/01
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ADENOSINE, PERIODATE OXIDIZED Chemical Properties,Usage,Production

Uses

Adenosine, periodate oxidized has been used:

  • as a methylarginine transferase inhibitor in the human embryonic kidney (HEK)-293 T cells
  • as a methylase inhibitor in H4 neuroglioma
  • as a broad inhibitor of S-adenosylmethionine (AdoMet)-dependent methyltransferases in mouse embryo fibroblast NIH3T3 cells

Uses

2-(1-(6-aMino-9H-purin-9-yl)-2-oxoethoxy)-3-hydroxypropanal is an inhibitor of S-adenosylhomocysteine hydrolase (AdoHcy hydrolase ) and it may be used in studies on the role of AdoHcy hydrolase in adenosine induce apoptosis and related S-adenosylhomocysteine-regulated processes. Adox is a methylation inhibitor that inhibits histone methytransferases (HMTase) and arginine methylation.

Biological Activity

adenosine dialdehyde (adox) has been identified as an indirect methyltransferase inhibitor.histone methyltransferases are a group of enzymes that catalyze the methylation of histone lysine and arginine by adding methyl groups to specific histone arginine or lysine residues.

Biochem/physiol Actions

Adenosine, periodate oxidized (Adox) is a protein arginine methyltransferases (PRMTs) inhibitor. It also inhibits the enzyme S-adenosylhomocysteine hydrolase and induces apoptosis. Its inhibitory effect on histone methyltransferases prevents histone methylation. Adox also elicits intrinsic cytotoxic properties.

in vitro

previous cell-based study showed that the treatment of cells with the methyltransferase inhibitor adenosine dialdehyde (adox) could lead to cell cycle arrest and death in different tested cell types. in addition, the e form of cell death and phenotypical outcom was found to be strikingly dependent on the concentration of adox. results showed that lower adox concentrations could result in a g2 arrest and predominantly cause apoptosis, which was measured by biochemical and morphological criteria. in contrast, higher concentrations of adox led to a novel and so far undescribed form of cell death that was characterized by distinct, caspase-independent alterations of the cell shape with a marked protuberation of the nucleus, actin aggregation, cytoplasmic extensions, as well as incomplete chromatin condensation [1].

References

[1] schwerk c, schulze-osthoff k. methyltransferase inhibition induces p53-dependent apoptosis and a novel form of cell death. oncogene.2005 oct 27;24(47):7002-11.

ADENOSINE, PERIODATE OXIDIZED Preparation Products And Raw materials

Raw materials

Preparation Products

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34240-05-6, ADENOSINE, PERIODATE OXIDIZEDRelated Search:


  • ADENOSINE, PERIODATE OXIDIZED
  • ADENOSINE-2',3'-DIALDEHYDE
  • 6-amino-alpha-(1-formyl-2-hydroxyethoxy)-9h-purine-9-acetaldehyd
  • AdenosineDialdehyde(ADOX)
  • 2-(1-(6-aMino-9H-purin-9-yl)-2-oxoethoxy)-3-hydroxypropanal
  • 6-amino-alpha-(1-formyl-2-hydroxyethoxy)-9h-purine-9-acetaldehyde
  • periodate-oxidizedadenosine
  • 9H-Purine-9-acetaldehyde, 6-amino-alpha-(1-formyl-2-hydroxyethoxy)-
  • alpha-(Hydroxymethyl)-alpha'-(6-aminopurin-9-yl)diglycolaldehyde
  • Hydracrylaldehyde, 2-((6-amino-9H-purin-9-yl)formylmethoxy)-
  • 9H-Purine-9-acetaldehyde, 6-amino-α-(1-formyl-2-hydroxyethoxy)-
  • Adenosine, periodate oxidized >=93%
  • 34240-05-6
  • BioChemical
  • Biochemicals and Reagents
  • Nucleosides
  • Nucleosides, Nucleotides, Oligonucleotides
  • Aldehydes
  • Biochemicals and Reagents
  • Building Blocks
  • C10-C12
  • Carbonyl Compounds
  • Chemical Synthesis
  • Nucleosides
  • Nucleotides
  • Oligonucleotides
  • Organic Building Blocks