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N6-(P-AMINOBENZYL)ADENOSINE

N6-(P-AMINOBENZYL)ADENOSINE Structure
N6-(P-AMINOBENZYL)ADENOSINE
  • CAS No.95523-13-0
  • Chemical Name:N6-(P-AMINOBENZYL)ADENOSINE
  • CBNumber:CB7496943
  • Molecular Formula:C17H20N6O4
  • Formula Weight:372.38
  • MOL File:95523-13-0.mol
N6-(P-AMINOBENZYL)ADENOSINE Property
  • 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
Hazard and Precautionary Statements (GHS)
  • Symbol(GHS)
  • Signal word
  • Hazard statements
  • Precautionary statements

N6-(P-AMINOBENZYL)ADENOSINE Chemical Properties,Usage,Production

  • 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)ADENOSINE Preparation Products And Raw materials
Raw materials
Preparation Products
N6-(P-AMINOBENZYL)ADENOSINE Suppliers
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N6-(P-AMINOBENZYL)ADENOSINE Spectrum
95523-13-0, N6-(P-AMINOBENZYL)ADENOSINERelated Search:
  • 抑制剂
  • (2R,3R,4S,5R)-2-(6-((4-氨基苄基)氨基)-9H-嘌呤-9-基)-5-(羟甲基)四氢呋喃-3,4-二醇
  • 化合物 T16166
  • N-[(4-氨基苯基)甲基]腺苷
  • 95523-13-0
  • (2R,3R,4S,5R)-2-(6-((4-Aminobenzyl)amino)-9H-purin-9-yl)-5-(hydroxymethyl)tetrahydrofuran-3,4-diol
  • N [(4 Aminophenyl)methyl]adenosine,N[(4Aminophenyl)methyl]adenosine
  • Adenosine, N-[(4-aminophenyl)methyl]-
  • [125I]-N6-(4-Aminobenzyl)adenosine
  • N6-(P-AMINOBENZYL)ADENOSINE
  • N-[(4-Aminophenyl)methyl]adenosine
  • N(sup 6)(p-aminobenzyl)adenosine

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