-
1
-
-
0036008097
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
11
-
-
35548947600
-
Proteome analyses of the growth inhibitory effects of NCH-51, a novel histone deacetylase inhibitor, on lymphoid malignant cells
-
Sanda, T.; Okamoto, T.; Uchida, Y.; Nakagawa, H.; Iida, S.; Kayukawa, S.; Suzuki, T.; Oshizawa, T.; Suzuki, T.; Miyata, N.; Ueda, R. Proteome analyses of the growth inhibitory effects of NCH-51, a novel histone deacetylase inhibitor, on lymphoid malignant cells Leukemia 2007, 21, 2344-2353
-
(2007)
Leukemia
, vol.21
, pp. 2344-2353
-
-
Sanda, T.1
Okamoto, T.2
Uchida, Y.3
Nakagawa, H.4
Iida, S.5
Kayukawa, S.6
Suzuki, T.7
Oshizawa, T.8
Suzuki, T.9
Miyata, N.10
Ueda, R.11
-
12
-
-
20044390016
-
Role of thioredoxin in the response of normal and transformed cells to histone deacetylase inhibitors
-
Ungerstedt, J. S.; Sowa, Y.; Xu, W. S.; Shao, Y.; Dokmanovic, M.; Perez, G.; Ngo, L.; Holmgren, A.; Jiang, X.; Marks, P. A. Role of thioredoxin in the response of normal and transformed cells to histone deacetylase inhibitors Proc. Natl. Acad. Sci. U.S.A. 2005, 102, 673-678
-
(2005)
Proc. Natl. Acad. Sci. U.S.A.
, vol.102
, pp. 673-678
-
-
Ungerstedt, J.S.1
Sowa, Y.2
Xu, W.S.3
Shao, Y.4
Dokmanovic, M.5
Perez, G.6
Ngo, L.7
Holmgren, A.8
Jiang, X.9
Marks, P.A.10
-
13
-
-
84899874384
-
Zur kenntnis der thiazol-2-carbonsäure
-
Erlenmeyer, H.; Marbet, R.; Schenkel, H. Zur kenntnis der thiazol-2-carbonsäure Helv. Chim. Acta 1945, 28, 924
-
(1945)
Helv. Chim. Acta
, vol.28
, pp. 924
-
-
Erlenmeyer, H.1
Marbet, R.2
Schenkel, H.3
-
14
-
-
79952050537
-
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
-
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
-
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
-
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
-
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
-
19
-
-
84866856929
-
1 receptor
-
1 receptor J. Med. Chem. 2012, 55, 8047-8065
-
(2012)
J. Med. Chem.
, vol.55
, pp. 8047-8065
-
-
Meyer, C.1
Schepmann, D.2
Yanagisawa, S.3
Yamaguchi, J.4
Dal Col, V.5
Laurini, E.6
Itami, K.7
Pricl, S.8
Wünsch, B.9
-
20
-
-
84891720942
-
Class i HDACs share a common mechanism of regulation by inositol phosphates
-
Millard, C. J.; Watson, P. J.; Celardo, I.; Gordiyenko, Y.; Cowley, S. M.; Robinson, C. V.; Fairall, L.; Schwabe, J. W. Class I HDACs share a common mechanism of regulation by inositol phosphates Mol. Cell 2013, 51, 57-67
-
(2013)
Mol. Cell
, vol.51
, pp. 57-67
-
-
Millard, C.J.1
Watson, P.J.2
Celardo, I.3
Gordiyenko, Y.4
Cowley, S.M.5
Robinson, C.V.6
Fairall, L.7
Schwabe, J.W.8
-
21
-
-
84890449949
-
Exploring the chemical space of multitarget ligands using aligned self-organizing maps
-
Achenbach, J.; Klingler, F. M.; Blöcher, R.; Moser, D.; Häfner, A. K.; Rödl, C. B.; Kretschmer, S.; Krüger, B.; Löhr, F.; Stark, H.; Hofmann, B.; Steinhilber, D.; Proschak, E. Exploring the chemical space of multitarget ligands using aligned self-organizing maps ACS Med. Chem. Lett. 2013, 4, 1169-1172
-
(2013)
ACS Med. Chem. Lett.
, vol.4
, pp. 1169-1172
-
-
Achenbach, J.1
Klingler, F.M.2
Blöcher, R.3
Moser, D.4
Häfner, A.K.5
Rödl, C.B.6
Kretschmer, S.7
Krüger, B.8
Löhr, F.9
Stark, H.10
Hofmann, B.11
Steinhilber, D.12
Proschak, E.13
-
22
-
-
77249170294
-
Rational design of indoleamine 2,3-dioxygenase inhibitors
-
Röhrig, U. F.; Awad, L.; Grosdidier, A.; Larrieu, P.; Stroobant, V.; Colau, D.; Cerundolo, V.; Simpson, A. J.; Vogel, P.; Van den Eynde, B. J.; Zoete, V.; Michielin, O. Rational design of indoleamine 2,3-dioxygenase inhibitors J. Med. Chem. 2010, 53, 1172-1189
-
(2010)
J. Med. Chem.
, vol.53
, pp. 1172-1189
-
-
Röhrig, U.F.1
Awad, L.2
Grosdidier, A.3
Larrieu, P.4
Stroobant, V.5
Colau, D.6
Cerundolo, V.7
Simpson, A.J.8
Vogel, P.9
Van Den Eynde, B.J.10
Zoete, V.11
Michielin, O.12
-
23
-
-
0035282632
-
Thiazole and thiadiazole analogues as a novel class of adenosine receptor antagonists
-
van Muijlwijk-Koezen, J. E.; Timmerman, H.; Vollinga, R. C.; Frijtag von Drabbe Künzel, J.; de Groote, M.; Visser, S.; IJzerman, A. P. Thiazole and thiadiazole analogues as a novel class of adenosine receptor antagonists J. Med. Chem. 2001, 44, 749-762
-
(2001)
J. Med. Chem.
, vol.44
, pp. 749-762
-
-
Van Muijlwijk-Koezen, J.E.1
Timmerman, H.2
Vollinga, R.C.3
Frijtag Von Drabbe Künzel, J.4
De Groote, M.5
Visser, S.6
Ijzerman, A.P.7
-
24
-
-
79955691468
-
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
|