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P7–2302

P7-2302 is a potent dual inhibitor of PDE7 (IC50=0.18 nM) and PDE4B (IC50=77.3 nM) that also modulates P-gp/BCRP efflux. Its low brain uptake and suitability for 18F-labeling make it a valuable PET tracer candidate for in vivo imaging and in vitro studies of phosphodiesterase function and transporter interactions.

Product Specifications

Field of Research

Metabolism Research

Molecular Formula

C23H21ClF2N2O4

Molecular Weight

462.87

Storage Conditions

-20°C

Notes

For research use only.

Available Sizes

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