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CM-675

CM-675
CM-675 is a dual inhibitor of phosphodiesterase 5 (PDE5) and class I histone deacetylases (IC50s: 114 nM and 673 nM for PDE5 and HDAC1) with the potential to treat Alzheimer’s disease.
Catalog No. T10841Cas No. 1872466-47-1
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Purity:99.67%
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CM-675

Catalog No. T10841Cas No. 1872466-47-1

CM-675 is a dual inhibitor of phosphodiesterase 5 (PDE5) and class I histone deacetylases (IC50s: 114 nM and 673 nM for PDE5 and HDAC1) with the potential to treat Alzheimer’s disease.
All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.
Pack SizePriceAvailabilityQuantity
1 mg$58In Stock
2 mg$87In Stock
5 mg$148In Stock
10 mg$238In Stock
25 mg$397In Stock
50 mg$567In Stock
100 mg$768In Stock
1 mL x 10 mM (in DMSO)$163In Stock
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Product Introduction

Bioactivity
Description
CM-675 is a dual inhibitor of phosphodiesterase 5 (PDE5) and class I histone deacetylases (IC50s: 114 nM and 673 nM for PDE5 and HDAC1) with the potential to treat Alzheimer’s disease.
Targets&IC50
PDE5:114 nM nM
In vitro
CM-675 (29a) demonstrates a pronounced time-dependent inhibitory effect on class I HDACs, particularly HDAC2. Its potency against HDAC1 also significantly enhances over time, showing increased inhibition (~1 log unit) at varying pre-incubation intervals: 673 nM at 30 minutes, 180 nM at 4 hours, and 69 nM at 6 hours[1].
Chemical Properties
Molecular Weight536.62
FormulaC31H32N6O3
Cas No.1872466-47-1
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 22.5 mg/mL (41.9 mM), Sonication and heating to 60℃ are recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM1.8635 mL9.3176 mL18.6352 mL93.1758 mL
5 mM0.3727 mL1.8635 mL3.7270 mL18.6352 mL
10 mM0.1864 mL0.9318 mL1.8635 mL9.3176 mL
20 mM0.0932 mL0.4659 mL0.9318 mL4.6588 mL

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