Ciladopa hydrochloride

PDE2/PDE10-IN-1 is a phosphodiesterase 2 ( PDE2 ) and PDE10 inhibitor with IC 50 s of 29 and 480 nM, respectively.In VitroPDE2/PDE10-IN-1 (Compound 6) inhibits PDE2 and PDE10, respectively, with an IC 50 value of 29 and 480 nM. PDE2/PDE10-IN-1 also

PDE2/PDE10-IN-1 is a phosphodiesterase 2 ( PDE2 ) and PDE10 inhibitor with IC 50 s of 29 and 480 nM, respectively.In VitroPDE2/PDE10-IN-1 (Compound 6) inhibits PDE2 and PDE10, respectively, with an IC 50 value of 29 and 480 nM. PDE2/PDE10-IN-1 also

PDE9-IN-1 is a potent, selective, and orally bioavailable phosphodiesterase-9A (PDE9A) Inhibitor with an IC 50 of 8.7 nMIn VitroPDE9-IN-1 is excellent selectivity across PDE families. MCE has not independently confirmed the accuracy of these

PDE9-IN-1 is a potent, selective, and orally bioavailable phosphodiesterase-9A (PDE9A) Inhibitor with an IC 50 of 8.7 nMIn VitroPDE9-IN-1 is excellent selectivity across PDE families. MCE has not independently confirmed the accuracy of these

PDE9-IN-1 is a potent, selective, and orally bioavailable phosphodiesterase-9A (PDE9A) Inhibitor with an IC 50 of 8.7 nMIn VitroPDE9-IN-1 is excellent selectivity across PDE families. MCE has not independently confirmed the accuracy of these

PDE9-IN-1 is a potent, selective, and orally bioavailable phosphodiesterase-9A (PDE9A) Inhibitor with an IC 50 of 8.7 nMIn VitroPDE9-IN-1 is excellent selectivity across PDE families. MCE has not independently confirmed the accuracy of these

Potent and selective PDE2A inhibitor.

Potent and selective PDE2A inhibitor.

PF-04745637 is a potent and selective TRPA1 antagonist with an IC 50 of 17 nM for human TRPA1In VivoTopically applied PF-04745637 (Compound 8: 50 mg/mL and 100 mg/mL) significantly reduces cinnamaldehyde-mediated flare in rat skin . MCE has not

PF-05085727 is a potent, selective and brain penetrant inhibitor of cGMP-dependent PDE2A ( IC 50 =2 nM). PF-05085727 inhibits PDE2A &gt:4,000-fold selectivity over PDE1 and PDE3-11In VitroPF-05085727 shows weak activity with IC 50 of 162 μM to

PF-05085727 is a potent, selective and brain penetrant inhibitor of cGMP-dependent PDE2A ( IC 50 =2 nM). PF-05085727 inhibits PDE2A &gt:4,000-fold selectivity over PDE1 and PDE3-11In VitroPF-05085727 shows weak activity with IC 50 of 162 μM to

PF-05085727 is a potent, selective and brain penetrant inhibitor of cGMP-dependent PDE2A ( IC 50 =2 nM). PF-05085727 inhibits PDE2A &gt:4,000-fold selectivity over PDE1 and PDE3-11In VitroPF-05085727 shows weak activity with IC 50 of 162 μM to