Synthesis of 2-quinolinecarboxamide derivatives as potential HDAC inhibitors
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[1] P. Bertrand. Inside HDAC with HDAC inhibitors. , 2010, European journal of medicinal chemistry.
[2] C. Supuran,et al. Carbonic anhydrase inhibitors. The nematode alpha-carbonic anhydrase of Caenorhabditis elegans CAH-4b is highly inhibited by 2-(hydrazinocarbonyl)-3-substituted-phenyl-1H-indole-5-sulfonamides. , 2009, Bioorganic & medicinal chemistry.
[3] Ivars Kalvinsh,et al. Novel amide derivatives as inhibitors of histone deacetylase: design, synthesis and SAR. , 2009, European journal of medicinal chemistry.
[4] M. Binaschi,et al. Histone deacetylase inhibitors: from bench to clinic. , 2008, Journal of medicinal chemistry.
[5] K. Glaser,et al. Histone deacetylase inhibitors: the Abbott experience. , 2003, Current medicinal chemistry.
[6] G Brosch,et al. Amide analogues of trichostatin A as inhibitors of histone deacetylase and inducers of terminal cell differentiation. , 1999, Journal of medicinal chemistry.
[7] J. Frère,et al. Phosphonamidate analogues of dipeptides with carboxypeptidase A and beta-lactamase-inhibitory activity: elucidation of the mechanism of beta-lactamase inhibition by electrospray mass spectrometry. , 1996, The Biochemical journal.
[8] M. Körner,et al. Histone deacetylase inhibitors: a novel class of anti-cancer agents on its way to the market. , 2008, Progress in medicinal chemistry.