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Cobicistat

Cat. No. M2537
Cobicistat  Structure
Synonym:

GS-9350

Size Price Availability Quantity
10mg USD 165  USD165 In stock
50mg USD 490  USD490 In stock
100mg USD 700  USD700 In stock
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Quality Control & Documentation
Biological Activity

Cobicistat (GS-9350) is a potent and selective inhibitor of CYP3A with IC50 of 30-285 nM.

Chemical Information
Molecular Weight 776.02
Formula C40H53N7O5S2
CAS Number 1004316-88-4
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] Lianhong Xu, et al. ACS Med Chem Lett. Cobicistat (GS-9350): A Potent and Selective Inhibitor of Human CYP3A as a Novel Pharmacoenhancer

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Keywords: Cobicistat , GS-9350 supplier, Cytochrome P450 (e.g. CYP17), inhibitors, activators


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