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Aristeromycin 

Cat. No. M29022
Aristeromycin  Structure
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Biological Activity

Aristeromycin, an adenosine analog, is an antibiotic and a potent S-adenosylhomocysteine hydrolase (AHCY) inhibitor.

Chemical Information
Molecular Weight 265.27
Formula C11H15N5O3
CAS Number 19186-33-5
Form Solid
Solubility (25°C) DMSO 50 mg/mL (ultrasonic and warming and heat to 60°C)
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] Alex J Vendola, et al. Org Lett. Diastereoselective Diboration of Cyclic Alkenes: Application to the Synthesis of Aristeromycin

[2] Ji-Seong Yoon, et al. J Med Chem. Design, Synthesis, and Anti-RNA Virus Activity of 6'-Fluorinated-Aristeromycin Analogues

[3] Noriko Uchiyama, et al. Eur J Pharmacol. Aristeromycin and DZNeP cause growth inhibition of prostate cancer via induction of mir-26a

[4] Weikuan Li, et al. Bioorg Med Chem Lett. 5'-Fluoro-5'-deoxyaristeromycin

[5] S Liu, et al. J Med Chem. Aristeromycin-5'-carboxaldehyde: a potent inhibitor of S-adenosyl-L-homocysteine hydrolase

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