N6-(P-AMINOBENZYL)ADENOSINE
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
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
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
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