Basic information Safety Supplier Related

N6-(P-AMINOBENZYL)ADENOSINE

Basic information Safety Supplier Related

N6-(P-AMINOBENZYL)ADENOSINE Basic information

Product Name:
N6-(P-AMINOBENZYL)ADENOSINE
Synonyms:
  • [125I]-N6-(4-Aminobenzyl)adenosine
  • N(sup 6)(p-aminobenzyl)adenosine
  • N-[(4-Aminophenyl)methyl]adenosine
  • N6-(P-AMINOBENZYL)ADENOSINE
  • Adenosine, N-[(4-aminophenyl)methyl]-
  • N [(4 Aminophenyl)methyl]adenosine,N[(4Aminophenyl)methyl]adenosine
  • (2R,3R,4S,5R)-2-(6-((4-Aminobenzyl)amino)-9H-purin-9-yl)-5-(hydroxymethyl)tetrahydrofuran-3,4-diol
CAS:
95523-13-0
MF:
C17H20N6O4
MW:
372.38
Mol File:
95523-13-0.mol
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N6-(P-AMINOBENZYL)ADENOSINE Chemical Properties

Boiling point:
749.0±70.0 °C(Predicted)
Density 
1.71±0.1 g/cm3(Predicted)
storage temp. 
2-8°C
solubility 
Soluble in DMSO
pka
13.12±0.70(Predicted)
form 
Solid
color 
Off-white to light yellow
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N6-(P-AMINOBENZYL)ADENOSINE Usage And Synthesis

Uses

N-[(4-Aminophenyl)methyl]adenosine is a adenosine receptor inhibitor, with Ki of 29 nM for Rat ecto-5′-Nucleotidase. IC50 value: 29.0 ± 1.7 nM (Ki) Target: Adenosine Receptor

References

[1] Bhattarai S, et al. α,β-Methylene-ADP (AOPCP) Derivatives and Analogues: Development of Potent and Selective ecto-5'-Nucleotidase (CD73) Inhibitors. J Med Chem. 2015 Aug 13;58(15):6248-63. DOI:10.1021/acs.jmedchem.5b00802
[2] Chen JB, et al. Design and synthesis of novel dual-action compounds targeting the adenosine A(2A) receptor and adenosine transporter for neuroprotection. ChemMedChem. 2011 Aug 1;6(8):1390-400. DOI:10.1002/cmdc.201100126
[3] Zhu Z, et al. Constrained NBMPR analogue synthesis, pharmacophore mapping and 3D-QSAR modeling of equilibrative nucleoside transporter 1 (ENT1) inhibitory activity. Bioorg Med Chem. 2008 Apr 1;16(7):3848-65. DOI:10.1016/j.bmc.2008.01.044

N6-(P-AMINOBENZYL)ADENOSINESupplier

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