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Capadenoson

Cat. No. M9799

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Capadenoson Structure
Synonym:

BAY 68-4986

Size Price Availability Quantity
5mg USD 70 In stock
10mg USD 100 In stock
25mg USD 200 In stock
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Quality Control & Documentation
Biological Activity

Capadenoson (BAY 68-4986) is an oral active, potent and selective adenosine A1 receptor agonist. In vivo, Wistar rats and SHR are pre-treated with Capadenoson at a concentration of 0.15 mg/kg for 5 days. On day 5, a stress test (physical restraint) is performed for 2 hours. The plasma concentration of Capadenoson measured 3 hours after drug intake remains constant in the 5 days prior to the restraint stress test and averaged 7.63 µg/L on day 4 and 5, respectively.

Chemical Information
Molecular Weight 520.03
Formula C25H18ClN5O2S2
CAS Number 544417-40-5
Solubility (25°C) DMSO ≥ 40 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Isaac R Bailey, et al. J Pharmacol Exp Ther. Optimization of Thermolytic Response to A 1 Adenosine Receptor Agonists in Rats

[2] Julien Louvel, et al. Eur J Med Chem. Structure-kinetics relationships of Capadenoson derivatives as adenosine A1 receptor agonists

[3] Lorenz Bott-Flugel, et al. PLoS One. Selective attenuation of norepinephrine release and stress-induced heart rate increase by partial adenosine A1 agonism

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Keywords: Capadenoson, BAY 68-4986 supplier, Adenosine Receptor, inhibitors, activators

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