Mocetinostat (MGCD0103)

Catalog #
27109
$380 *
Size: 5 mg
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Description

Mocetinostat (MGCD0103) is an HDAC inhibitor. It was shown to induce hyperacetylation of histones resulting in cancer cell selective apoptosis, and cause cell cycle blockade in various human cancer cell lines in a dose-dependent manner. Mocetinostat inhibites growth of human tumor xenografts in nude mice in a dose-dependent manner and its antitumor activity correlates with induction of histone acetylation in tumors.

Synonyms
MGCD0103
Product Info
Storage and Usage
Citations
Purity

≥99% by HPLC

Format
A crystalline solid
Formula
C23H20N6O
MW
396.4 Da
Solubility
Solubility in DMSO is 13 mg/ml, and in water and ethanol is < 1 mg/ml. DMSO stock solutions are stable up to one week at 4ºC or up to a month at -70ºC. Do not store aqueous solutions for more than one day.
Biological Activity
Mocetinostat (MGCD0103) inhibits HDAC1, HDAC2 and HDAC3 with IC50 values of 0.15 µM, 0.29 µM and 1.66 µM, respectively.
CAS Registry #
726169-73-9
References
1. Foumel, M., et al., Mol Cancer Ther. 2008;7:759-768.
2. Duque-Afonso, J., et al. Oncogene 2011. July;30:3062-72.
3. Munkacsi, A.B., et al. J. Biol. Chem. 2011. July;286:23842-51.
4. Xu, X., et al. PLoS ONE. February 2011. 6:e17138.