메뉴 건너뛰기




Volumn 5, Issue 5, 2014, Pages 582-586

Late-stage C-H coupling enables rapid identification of HDAC inhibitors: Synthesis and evaluation of NCH-31 analogues

Author keywords

C H coupling; HDAC6; Histone deacetylase; inhibitor

Indexed keywords

2 AMINOTHIAZOLE DERIVATIVE; HISTONE DEACETYLASE 1; HISTONE DEACETYLASE 6; HISTONE DEACETYLASE 9; HISTONE DEACETYLASE INHIBITOR; UNCLASSIFIED DRUG;

EID: 84900392663     PISSN: None     EISSN: 19485875     Source Type: Journal    
DOI: 10.1021/ml500024s     Document Type: Article
Times cited : (29)

References (25)
  • 1
    • 0036008097 scopus 로고    scopus 로고
    • Deacetylase enzymes: Biological functions and the use of small-molecule inhibitors
    • Grozinger, C. M.; Schreiber, S. L. Deacetylase enzymes: Biological functions and the use of small-molecule inhibitors Chem. Biol. 2002, 9, 3-16
    • (2002) Chem. Biol. , vol.9 , pp. 3-16
    • Grozinger, C.M.1    Schreiber, S.L.2
  • 2
    • 28044471827 scopus 로고    scopus 로고
    • Acetylation and deacetylation of non-histone proteins
    • Glozak, M. A.; Sengupta, N.; Zhang, X.; Seto, E. Acetylation and deacetylation of non-histone proteins Gene 2005, 363, 15-23
    • (2005) Gene , vol.363 , pp. 15-23
    • Glozak, M.A.1    Sengupta, N.2    Zhang, X.3    Seto, E.4
  • 3
    • 0642286534 scopus 로고    scopus 로고
    • Protein deacetylases: Enzymes with functional diversity as novel therapeutic targets
    • Yoshida, M.; Shimazu, T.; Matsuyama, A. Protein deacetylases: enzymes with functional diversity as novel therapeutic targets Prog. Cell Cycle Res. 2003, 5, 269-278
    • (2003) Prog. Cell Cycle Res. , vol.5 , pp. 269-278
    • Yoshida, M.1    Shimazu, T.2    Matsuyama, A.3
  • 4
    • 42049118549 scopus 로고    scopus 로고
    • Isoform-selective histone deacetylase inhibitors
    • Itoh, Y.; Suzuki, T.; Miyata, N. Isoform-selective histone deacetylase inhibitors Curr. Pharm. Des. 2008, 14, 529-544
    • (2008) Curr. Pharm. Des. , vol.14 , pp. 529-544
    • Itoh, Y.1    Suzuki, T.2    Miyata, N.3
  • 5
    • 84875867286 scopus 로고    scopus 로고
    • Small-molecular modulators of cancer-associated epigenetic mechanisms
    • Itoh, Y.; Suzuki, T.; Miyata, N. Small-molecular modulators of cancer-associated epigenetic mechanisms Mol. Biosyst. 2013, 9, 873-896
    • (2013) Mol. Biosyst. , vol.9 , pp. 873-896
    • Itoh, Y.1    Suzuki, T.2    Miyata, N.3
  • 6
    • 33846122993 scopus 로고    scopus 로고
    • Dimethyl sulfoxide to vorinostat: Development of this histone deacetylase inhibitor as an anticancer drug
    • Marks, P. A.; Breslow, R. Dimethyl sulfoxide to vorinostat: development of this histone deacetylase inhibitor as an anticancer drug Nat. Biotechnol. 2007, 25, 84-90
    • (2007) Nat. Biotechnol. , vol.25 , pp. 84-90
    • Marks, P.A.1    Breslow, R.2
  • 7
    • 79960356610 scopus 로고    scopus 로고
    • Romidepsin: A novel histone deacetylase inhibitor for cancer
    • Bertino, E. M.; Otterson, G. A. Romidepsin: a novel histone deacetylase inhibitor for cancer Expert Opin. Invest. Drugs 2011, 20, 1151-1158
    • (2011) Expert Opin. Invest. Drugs , vol.20 , pp. 1151-1158
    • Bertino, E.M.1    Otterson, G.A.2
  • 8
    • 41149089267 scopus 로고    scopus 로고
    • Histone deacetylase inhibitors: From bench to clinic
    • Paris, M.; Porcelloni, M.; Binaschi, M.; Fattori, D. Histone deacetylase inhibitors: from bench to clinic J. Med. Chem. 2008, 51, 1505-1529
    • (2008) J. Med. Chem. , vol.51 , pp. 1505-1529
    • Paris, M.1    Porcelloni, M.2    Binaschi, M.3    Fattori, D.4
  • 9
    • 13944254995 scopus 로고    scopus 로고
    • Novel inhibitors of human histone deacetylases: Design, synthesis, enzyme inhibition, and cancer cell growth inhibition of SAHA-based non-hydroxamates
    • Suzuki, T.; Nagano, Y.; Kouketsu, A.; Matsuura, A.; Maruyama, S.; Kurotaki, M.; Nakagawa, H.; Miyata, N. Novel inhibitors of human histone deacetylases: design, synthesis, enzyme inhibition, and cancer cell growth inhibition of SAHA-based non-hydroxamates J. Med. Chem. 2005, 48, 1019-1032
    • (2005) J. Med. Chem. , vol.48 , pp. 1019-1032
    • Suzuki, T.1    Nagano, Y.2    Kouketsu, A.3    Matsuura, A.4    Maruyama, S.5    Kurotaki, M.6    Nakagawa, H.7    Miyata, N.8
  • 10
    • 0038274087 scopus 로고    scopus 로고
    • Structural biasing elements for in-cell histone deacetylase paralog selectivity
    • Wong, J. C.; Hong, R.; Schreiber, S. L. Structural biasing elements for in-cell histone deacetylase paralog selectivity J. Am. Chem. Soc. 2003, 125, 5586-5587
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 5586-5587
    • Wong, J.C.1    Hong, R.2    Schreiber, S.L.3
  • 14
    • 79952050537 scopus 로고    scopus 로고
    • Oxidative biaryl coupling of thiophenes and thiazoles with arylboronic acids through palladium catalysis: Otherwise difficult C4-selective C-H arylation enabled by boronic acids
    • Kirchberg, S.; Tani, S.; Ueda, K.; Yamaguchi, J.; Studer, A.; Itami, K. Oxidative biaryl coupling of thiophenes and thiazoles with arylboronic acids through palladium catalysis: otherwise difficult C4-selective C-H arylation enabled by boronic acids Angew. Chem., Int. Ed. 2011, 50, 2387-2391
    • (2011) Angew. Chem., Int. Ed. , vol.50 , pp. 2387-2391
    • Kirchberg, S.1    Tani, S.2    Ueda, K.3    Yamaguchi, J.4    Studer, A.5    Itami, K.6
  • 15
    • 84888580306 scopus 로고    scopus 로고
    • Programmed synthesis of arylthiazoles through sequential C-H couplings
    • Tani, S.; Uehara, T. N.; Yamaguchi, J.; Itami, K. Programmed synthesis of arylthiazoles through sequential C-H couplings Chem. Sci. 2014, 5, 123-135
    • (2014) Chem. Sci. , vol.5 , pp. 123-135
    • Tani, S.1    Uehara, T.N.2    Yamaguchi, J.3    Itami, K.4
  • 16
    • 84896285797 scopus 로고    scopus 로고
    • Palladium-catalyzed C-H and C-N arylation of aminothiazoles with arylboronic Acids
    • Uehara, T. N.; Yamaguchi, J.; Itami, K. Palladium-catalyzed C-H and C-N arylation of aminothiazoles with arylboronic Acids Asian J. Org. Chem. 2013, 2, 938-942
    • (2013) Asian J. Org. Chem. , vol.2 , pp. 938-942
    • Uehara, T.N.1    Yamaguchi, J.2    Itami, K.3
  • 17
    • 84865838463 scopus 로고    scopus 로고
    • C-H bond functionalization: Emerging synthetic tools for natural products and pharmaceuticals
    • Yamaguchi, J.; Yamaguchi, A. D.; Itami, K. C-H bond functionalization: emerging synthetic tools for natural products and pharmaceuticals Angew. Chem., Int. Ed. 2012, 51, 8960-9009
    • (2012) Angew. Chem., Int. Ed. , vol.51 , pp. 8960-9009
    • Yamaguchi, J.1    Yamaguchi, A.D.2    Itami, K.3
  • 18
    • 84876828644 scopus 로고    scopus 로고
    • C-H bond activation enables the rapid construction and late-stage diversification of functional molecules
    • Wencel-Delord, J.; Glorius, F. C-H bond activation enables the rapid construction and late-stage diversification of functional molecules Nat. Chem. 2013, 5, 369-375
    • (2013) Nat. Chem. , vol.5 , pp. 369-375
    • Wencel-Delord, J.1    Glorius, F.2
  • 24
    • 79955691468 scopus 로고    scopus 로고
    • Divergent C-H functionalizations directed by sulfonamide pharmacophores: Late-stage diversification as a tool for drug discovery
    • Dai, H.-X.; Stepan, A. F.; Plummer, M. S.; Zhang, Y.-H.; Yu, J.-Q. Divergent C-H functionalizations directed by sulfonamide pharmacophores: late-stage diversification as a tool for drug discovery J. Am. Chem. Soc. 2011, 133, 7222-7228
    • (2011) J. Am. Chem. Soc. , vol.133 , pp. 7222-7228
    • Dai, H.-X.1    Stepan, A.F.2    Plummer, M.S.3    Zhang, Y.-H.4    Yu, J.-Q.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.