Mocetinostat
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Preferred IUPAC name N-(2-Aminophenyl)-4-({[4-(pyridin-3-yl)pyrimidin-2-yl]amino}methyl)benzamide | |
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Chemical formula | C23H20N6O |
Molar mass | 396.454 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). N verify (what is YN ?) Infobox references |
Chemical compound
Mocetinostat (MGCD0103) is a benzamide histone deacetylase inhibitor undergoing clinical trials for treatment of various cancers including follicular lymphoma, Hodgkin's lymphoma and acute myelogenous leukemia.[1][2][3]
One clinical trial (for refractory follicular lymphoma) was temporarily put on hold due to cardiac problems but resumed recruiting in 2009.[4]
In 2010 favourable results were announced from the phase II trial for Hodgkin's lymphoma.[5]
MGCD0103 has also been used as a research reagent where blockage of members of the HDAC-family of histone deacetylases is required.[6]
Mechanism of action
It works by inhibiting mainly histone deacetylase 1 (HDAC1), but also HDAC2, HDAC3, and HDAC11.[7]
References
- ^ "Pharmion Corporation (PHRM) Release: Clinical Data On Oncology HDAC Inhibitor MGCD0103, Presented At The American Society of Clinical Oncology 42nd Annual Meeting" (Press release). Colorado, United States: BioSpace. June 6, 2006. Archived from the original on July 16, 2011.
- ^ Gelmon, K.; Tolcher, A.; Carducci, M.; Reid, G. K.; Li, Z.; Kalita, A.; Callejas, V.; Longstreth, J.; Besterman, J. M.; Siu, L. L. (2005). Phase I trials of the oral histone deacetylase (HDAC) inhibitor MGCD0103 given either daily or 3x weekly for 14 days every 3 weeks in patients (pts) with advanced solid tumors. 2005 ASCO Annual Meeting. J. Clin. Oncol. Vol. 23, no. 16S. 3147. Archived from the original on 2012-07-11.
- ^ MethylGene to Resume Development of its HDAC Inhibitor, MGCD0103 (Mocetinostat), Sept 2009
- ^ "METHYLGENE TO RESUME DEVELOPMENT OF ITS HDAC INHIBITOR, MGCD0103 (MOCETINOSTAT)". 21 Sep 2009. Archived from the original on 29 February 2012. Retrieved 13 September 2010.
- ^ "Final Phase 2 Clinical Data for Mocetinostat (MGCD0103) in Relapsed/Refractory Hodgkin Lymphoma Patients". 6 Dec 2010.
- ^ Pfefferli, Catherine; Müller, Fritz; Jaźwińska, Anna; Wicky, Chantal (2014). "Specific NuRD components are required for fin regeneration in zebrafish". BMC Biol. 12 (30): 30. doi:10.1186/1741-7007-12-30. PMC 4038851. PMID 24779377.
- ^ Fournel, Marielle; Bonfils, Claire; Hou, Yu; Yan, Pu Theresa; Trachy-Bourget, Marie-Claude; Kalita, Ann; Liu, Jianhong; Lu, Ai-Hua; Zhou, Nancy Z.; Robert, Marie-France; Gillespie, Jeffrey; Wang, James J.; Ste-Croix, Hélène; Rahil, Jubrail; Lefebvre, Sylvain (2008-04-01). "MGCD0103, a novel isotype-selective histone deacetylase inhibitor, has broad spectrum antitumor activity in vitro and in vivo". Molecular Cancer Therapeutics. 7 (4): 759–768. doi:10.1158/1535-7163.mct-07-2026. ISSN 1535-7163. PMID 18413790.
- v
- t
- e
- 3,3'-Diindolylmethane
- β-Hydroxybutyric acid (β-hydroxybutyrate)
- Abexinostat
- Acetoacetic acid (acetoacetate)
- Allyl mercaptan
- Apicidin
- Belinostat
- Butyric acid (butyrate)
- Capsaicin
- Citarinostat
- Curcumin
- Diallyl disulfide
- Entinostat
- Fimepinostat
- Givinostat
- Indole-3-carbinol
- Kevetrin
- Martinostat
- Mocetinostat
- Niacinamide
- Panobinostat
- Parthenolide
- Phenylbutyrate
- Pracinostat
- Quisinostat
- Resminostat
- Romidepsin
- Scriptaid
- Sodium butyrate
- Sodium oxybate (GHB sodium)
- Sodium phenylbutyrate
- Sodium valproate
- Sulforaphane
- Trapoxin B
- Trichostatin A
- Tucidinostat
- Valnoctamide
- Valproic acid (valproate)
- Valproate pivoxil
- Valproate semisodium
- Valpromide
- Vorinostat (SAHA)
See also: Receptor/signaling modulators