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AS1810722

Cat. No. M21381
AS1810722  Structure
Size Price Availability Quantity
5mg USD 300  USD300 In stock
10mg USD 480  USD480 In stock
25mg USD 950  USD950 In stock
50mg USD 1420  USD1420 In stock
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Quality Control & Documentation
Biological Activity

AS1810722 is an orally effective STAT6 inhibitor with an IC50 of 1.9 nM. AS1810722 shows good CYP3A4 inhibition and is a thickened bicyclic pyrimidine derivative with potential for use in allergic disease studies, such as asthma and atopic diseases.

Chemical Information
Molecular Weight 477.51
Formula C25H25F2N7O
CAS Number 909561-15-5
Solubility (25°C) DMSO ≥ 60 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] Shinya Nagashima, et al. Bioorg Med Chem. Novel 7H-pyrrolo[2,3-d]pyrimidine derivatives as potent and orally active STAT6 inhibitors

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  Catalog
Abmole Inhibitor Catalog




Keywords: AS1810722 supplier, STAT, inhibitors, activators


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