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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