>>Signaling Pathways>> Chromatin/Epigenetics>> HDAC>>CM-675

CM-675

Catalog No.GC65426

CM-675는 이중 포스포디에스테라제 5(PDE5) 및 클래스 I 히스톤 데아세틸라제 선택적 억제제로서 PDE5 및 HDAC1에 대해 각각 IC50 값이 114nM 및 673nM입니다.

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CM-675 Chemical Structure

Cas No.: 1872466-47-1

Size 가격 재고 수량
5mg
US$270.00
재고 있음
10mg
US$432.00
재고 있음

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Sample solution is provided at 25 µL, 10mM.

Description Protocol Chemical Properties Product Documents

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].

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].

[1]. Rabal O, et al. Discovery of in Vivo Chemical Probes for Treating Alzheimer's Disease: Dual Phosphodiesterase 5 (PDE5) and Class I Histone Deacetylase Selective Inhibitors. ACS Chem Neurosci. 2019 Mar 20;10(3):1765-1782.

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Average Rating: 5 ★★★★★ (Based on Reviews and 30 reference(s) in Google Scholar.)

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