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N6-(4-Hydroxybenzyl)adenosine

Cat. No. M38965
N6-(4-Hydroxybenzyl)adenosine Structure
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Biological Activity

N6-(4-Hydroxybenzyl)adenosine is a inhibitor of platelet aggregation induced in vitro by collagen and their activity range was demonstrated (IC50: 6.77-141 μM).

Chemical Information
Molecular Weight 373.36
Formula C17H19N5O5
CAS Number 110505-75-4
Form Solid
Solubility (25°C) DMSO ≥ 90 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
Conversion of different model animals based on BSA (PMID: 27057123)
Species Mouse Rat Rabbit Guinea pig Hamster Dog
Weight (kg) 0.02 0.15 1.8 0.4 0.08 10
Body Surface Area (m2) 0.007 0.025 0.15 0.05 0.02 0.5
Km factor 3 6 12 8 5 20
Animal A (mg/kg) = Animal B (mg/kg) multiplied by  Animal B Km
Animal A Km

For example, to modify the dose of Compound A used for a mouse (20 mg/kg) to a dose based on the BSA for a rat, multiply 20 mg/kg by the Km factor for a mouse and then divide by the Km factor for a rat. This calculation results in a rat equivalent dose for Compound A of 10 mg/kg.

References

[1] Wei-Hsiang Hsu et al. Aging (Albany NY). T1-11, an adenosine derivative, ameliorates aging-related behavioral physiology and senescence markers in aging mice

[2] Sa-Ik Hong et al. J Pharmacol Exp Ther. Novel Adenosine Analog, N 6-(4-Hydroxybenzyl)-Adenosine, Dampens Alcohol Drinking and Seeking Behaviors

[3] An-Hsun Chou et al. Neuropharmacology. T1-11 and JMF1907 ameliorate polyglutamine-expanded ataxin-3-induced neurodegeneration, transcriptional dysregulation and ataxic symptom in the SCA3 transgenic mouse

[4] Pavel Starha et al. Molecules. N6-benzyladenosine derivatives as novel N-donor ligands of platinum(II) dichlorido complexes

[5] Jhih-Bin Chen et al. ChemMedChem. Design and synthesis of novel dual-action compounds targeting the adenosine A(2A) receptor and adenosine transporter for neuroprotection

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Keywords: N6-(4-Hydroxybenzyl)adenosine supplier, P2 Receptor, inhibitors, activators


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