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Cyclic acid anhydrides as a new class of potent, selective and non-peptidic inhibitors of geranylgeranyl transferase.
Bioorg Med Chem Lett. 2002 Jan 21;12(2):255-9. doi: 10.1016/s0960-894x(01)00718-1.
Bioorg Med Chem Lett. 2002.
PMID: 11755366
Stereodefined and polyunsaturated inhibitors of histone deacetylase based on (2E,4E)-5-arylpenta-2,4-dienoic acid hydroxyamides.
Marson CM, Serradji N, Rioja AS, Gastaud SP, Alao JP, Coombes RC, Vigushin DM.
Marson CM, et al. Among authors: rioja as.
Bioorg Med Chem Lett. 2004 May 17;14(10):2477-81. doi: 10.1016/j.bmcl.2004.03.012.
Bioorg Med Chem Lett. 2004.
PMID: 15109636
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Aromatic sulfide inhibitors of histone deacetylase based on arylsulfinyl-2,4-hexadienoic acid hydroxyamides.
Marson CM, Savy P, Rioja AS, Mahadevan T, Mikol C, Veerupillai A, Nsubuga E, Chahwan A, Joel SP.
Marson CM, et al. Among authors: rioja as.
J Med Chem. 2006 Jan 26;49(2):800-5. doi: 10.1021/jm051010j.
J Med Chem. 2006.
PMID: 16420064
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The histone deacetylase inhibitor UCL67022 has potent activity in multiple myeloma and non-Hodgkin lymphoma pre-clinical models.
Maharaj L, Marson CM, Middleton BJ, Rioja AS, Perry J, Oakervee H, Cavenagh J, Joel SP, Popat R.
Maharaj L, et al. Among authors: rioja as.
Br J Haematol. 2013 Oct;163(1):135-9. doi: 10.1111/bjh.12456. Epub 2013 Jul 9.
Br J Haematol. 2013.
PMID: 23834265
Free article.
No abstract available.
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