95523-13-0
![N-[(4-Aminophenyl)methyl]adenosine Chemical Structure](http://file.medchemexpress.cn/product_pic/hy-100130.gif "N-[(4-Aminophenyl)methyl]adenosine Chemical Structure")
95523-13-0
Chemical Structure
N-[(4-Aminophenyl)methyl]adenosine
- CAS No.: 95523-13-0
- Formula:C17H20N6O4
- Molecular Weight:372.38
IUPAC Name: (2R,3R,4S,5R)-2-(6-((4-aminobenzyl)amino)-9H-purin-9-yl)-5-(hydroxymethyl)tetrahydrofuran-3,4-diol
InChIKey: PMUVNAUPWLXPSA-LSCFUAHRSA-N
SMILES: OC[C@@H]1[C@H]([C@H]([C@H](N2C=NC3=C2N=CN=C3NCC4=CC=C(N)C=C4)O1)O)O
Biological Activity:
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N-[(4-Aminophenyl)methyl]adenosine | 98.06% | N-[(4-Aminophenyl)methyl]adenosine is a adenosine receptor inhibitor, with Ki of 29 nM for Rat ecto-5′-Nucleotidase. | ||||||||||||||||||||
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N-[(4-Aminophenyl)methyl]adenosine (Standard) | ≥98% | N-[(4-Aminophenyl)methyl]adenosine (Standard) is the analytical standard of N-[(4-Aminophenyl)methyl]adenosine (HY-100130). This product is intended for research and analytical applications. 0 | ||||||||||||||||||||
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References
- 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. [Content Brief]
- 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. [Content Brief]
- 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. [Content Brief]
