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Cat. No.: HY-100130R

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N-[(4-Aminophenyl)methyl]adenosine (Standard)

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

For research use only. We do not sell to patients.

CAS No.: 95523-13-0
Formula: C₁₇H₂₀N₆O₄
Molecular Weight:372.38

Storage:

Please store the product under the recommended conditions in the Certificate of Analysis.

N-[(4-Aminophenyl)methyl]adenosine (Standard) Chemical Structure

CAS No.: 95523-13-0

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Strong Fluorescence Signal / Multi-Disciplinary Applications / High Fluorescence Specificity

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Product Information

Information

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

Application

The compound is the grade of analytical standard, which is the reference standard supplied assay. It is commonly used in qualitative, quantitative and methodological research experiments in HPLC, GC and MS.

Chemical Information

CAS No. 95523-13-0
Molecular Weight 372.38
Formula C₁₇H₂₀N₆O₄
SMILES

OC[C@@H]1[C@H]([C@H]([C@H](N2C=NC3=C2N=CN=C3NCC4=CC=C(N)C=C4)O1)O)O
Shipping

Room temperature in continental US; may vary elsewhere.
Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Purity & Documentation

Select Batch:

Purity: 99.98%

Assay: 99.98%

ee.: 99.98%

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. [Content Brief]

[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. [Content Brief]

[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. [Content Brief]

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Help & FAQs

How should lyophilized recombinant proteins be reconstituted and stored?

1. Before opening the cap, centrifuge the vial at 13000 rpm for 20-30 seconds. This step will ensure that any lyophilized powder that may have adhered to the cap or walls is collected at the bottom of the vial, minimizing the risk of product loss.

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N-[(4-Aminophenyl)methyl]adenosine (Standard)

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N-[(4-Aminophenyl)methyl]adenosine (Standard)

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