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Aliases: Mocetinostat; N-(2-aminophenyl)-4-[(4-pyridin-3-ylpyrimidin-2-ylamino)methyl]benzamide; MGCD010
商品コード: 14136 Format: 25 mg ¥57,000 Buy Now
商品コード: 14137 Format: 5 mg ¥18,400 Buy Now
Application: Histone Acetylation (HAT & HDAC)

for MocetinostatChemical Properties

MW = 396.4
CAS 726169-73-9
>98% (HPLC); NMR (Conforms)

for MocetinostatDescription

Class I, isoform-selective HDAC inhibitor (IC50 = 0.15, 0.29, 1.66 and 0.59 µM for HDAC1, 2, 3 and 11 respectively) (ref 1). Induces hyperacetylation of histones, induces expression of the tumor supressor p21WAF1 and inhibits proliferation of human cancer cells (ref 2). Displays antifibrotic effects in ischemic heart failure (ref 3). Attenuates the development of hypersensitivity in models of neuropathic pain (ref 4). Active in vivo (ref 5).

for MocetinostatContents

Off-white crystalline powder. May be dissolved in DMSO (25 mg/ml).

for MocetinostatReferences

1. N Zhou et al. J. Med. Chem. 2008, 51:4072
2. S Raeppel et al. Bioorg. Med. Chem. Lett. 2009, 19:644
3. H Nural-Govener et al. Int. J. Mol. Sci. 2015, 16:11482
4. F Denk et al. Pain 2013, 154:1668
5. C Bonfils et al. Clin. Cancer Res. 2008, 14:3441

Chemical structure of Mocetinostat.

Chemical structure of Mocetinostat.


Technical Data Sheet


Data Thumbnails

Chemical structure of Mocetinostat.

Chemical structure of Mocetinostat (click to enlarge.)