Hcyb1 is a highly selective, orally active PDE2 inhibitor. Hcyb1 has a highly selective inhibition of PDE2A (IC50=0.57 µM) and over 250-fold selectivity against other recombinant PDE family members. Hcyb1 produces neuroprotective and antidepressant-like effects most likely mediated by cAMP/cGMP-CREB-BDNF signaling[1].
Molekulargewicht:
380.44
Reinheit:
98.20
CAS Nummer:
[2988566-71-6]
Formel:
C24H20N4O
Target-Kategorie:
Phosphodiesterase (PDE)
Anwendungsbeschreibung:
MCE Product type: Reference compound
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