Name | CM-675 |
---|
Description | CM-675 is a dual phosphodiesterase 5 (PDE5) and class I histone deacetylases-selective inhibitor, with IC50 values of 114 nM and 673 nM for PDE5 and HDAC1, respectively. CM-675 has potential to treat Alzheimer’s disease[1]. |
---|---|
Related Catalog | |
Target |
HDAC1:673 nM (IC50, 30 min (time-dependent)) PDE5:114 nM nM (IC50) |
In Vitro | CM-675 (29a) shows a significant time-dependent effect on class I HDAC inhibition, particularly towards HDAC2. For HDAC1, its inhibitory potency also increased significantly (~1 log unit) with the pre-incubation time: 673 nM (30 min), 180 nM (4 hours) and 69 nM (6 hours) [1]. |
References |
Molecular Formula | C31H32N6O3 |
---|---|
Molecular Weight | 536.62 |