-
2
-
-
0037444803
-
Histone deacetylases (HDACs): Characterization of the classical HDAC family
-
De Ruijter AJM, Van Gennip AH, Caron HN, et al. Histone deacetylases (HDACs): characterization of the classical HDAC family. Biochem J 2003;370:737-49.
-
(2003)
Biochem J
, vol.370
, pp. 737-749
-
-
De Ruijter, A.J.M.1
Van Gennip, A.H.2
Caron, H.N.3
-
3
-
-
33745835064
-
Dissecting the biological functions of Drosophila histone deacetylases by RNA interference and transcriptional profiling
-
Foglietti C, Filocamo G, Cundari E, et al. Dissecting the biological functions of Drosophila histone deacetylases by RNA interference and transcriptional profiling. J Biol Chem 2006;281:17968-76.
-
(2006)
J Biol Chem
, vol.281
, pp. 17968-17976
-
-
Foglietti, C.1
Filocamo, G.2
Cundari, E.3
-
4
-
-
4944255743
-
Post-translational modification of p53 in tumorigenesis
-
Bode AM, Dong ZG. Post-translational modification of p53 in tumorigenesis. Nat Rev Cancer 2004;4:793-805.
-
(2004)
Nat Rev Cancer
, vol.4
, pp. 793-805
-
-
Bode, A.M.1
Dong, Z.G.2
-
5
-
-
2342522110
-
Shaping the nuclear action of NF-kappa B
-
Chen LF, Greene WC. Shaping the nuclear action of NF-kappa B. Nat Rev Mol Cell Bio 2004;5:392-401.
-
(2004)
Nat Rev Mol Cell Bio
, vol.5
, pp. 392-401
-
-
Chen, L.F.1
Greene, W.C.2
-
6
-
-
21144444486
-
HDAC6 regulates Hsp90 acetylation and chaperone-dependent activation of glucocorticoid receptor
-
Kovacs JJ, Murphy PJM, Gaillard S, et al. HDAC6 regulates Hsp90 acetylation and chaperone-dependent activation of glucocorticoid receptor. Mol Cell 2005;18:601-7.
-
(2005)
Mol Cell
, vol.18
, pp. 601-607
-
-
Kovacs, J.J.1
Murphy, P.J.M.2
Gaillard, S.3
-
7
-
-
0035755974
-
Histone deacetylases and cancer: Causes and therapies
-
Marks PA, Rifkind RA, Richon VM, et al. Histone deacetylases and cancer: causes and therapies. Nat Rev Cancer 2001;1:194-202.
-
(2001)
Nat Rev Cancer
, vol.1
, pp. 194-202
-
-
Marks, P.A.1
Rifkind, R.A.2
Richon, V.M.3
-
8
-
-
0036527775
-
Histone-deacetylase inhibitors: Novel drugs for the treatment of cancer
-
Johnstone RW. Histone-deacetylase inhibitors: novel drugs for the treatment of cancer. Nat Rev Drug Discov 2002;1:287-99.
-
(2002)
Nat Rev Drug Discov
, vol.1
, pp. 287-299
-
-
Johnstone, R.W.1
-
9
-
-
13444274622
-
Inhibitors of histone deacetylases induce tumor-selective apoptosis through activation of the death receptor pathway
-
Insinga A, Monestiroli S, Ronzoni S, et al. Inhibitors of histone deacetylases induce tumor-selective apoptosis through activation of the death receptor pathway. Nat Med 2005;11:233.
-
(2005)
Nat Med
, vol.11
, pp. 233
-
-
Insinga, A.1
Monestiroli, S.2
Ronzoni, S.3
-
10
-
-
0032539890
-
A class of hybrid polar inducers of transformed cell differentiation inhibits histone deacetylases
-
Richon VM, Emiliani S, Verdin E, et al. A class of hybrid polar inducers of transformed cell differentiation inhibits histone deacetylases. P Natl Acad Sci USA 1998;95:3003-7.
-
(1998)
P Natl Acad Sci USA
, vol.95
, pp. 3003-3007
-
-
Richon, V.M.1
Emiliani, S.2
Verdin, E.3
-
11
-
-
0028258610
-
Fr901228, a novel antitumor bicyclic depsipeptide produced by chromobacterium-violaceum no-968.1. Taxonomy, fermentation, isolation, physicochemical and biological properties, and antitumor-activity
-
Ueda H, Nakajima H, Hori Y, et al. Fr901228, a novel antitumor bicyclic depsipeptide produced by chromobacterium-violaceum no-968.1. Taxonomy, fermentation, isolation, physicochemical and biological properties, and antitumor-activity. J Antibiot 1994;47: 301-10.
-
(1994)
J Antibiot
, vol.47
, pp. 301-310
-
-
Ueda, H.1
Nakajima, H.2
Hori, Y.3
-
12
-
-
84861917256
-
Discovery of a novel histone deacetylase 8 inhibitor by virtual screening
-
Zhang L, Li MY, Feng JH, et al. Discovery of a novel histone deacetylase 8 inhibitor by virtual screening. Med Chem Res 2012; 21:152-6.
-
(2012)
Med Chem Res
, vol.21
, pp. 152-156
-
-
Zhang, L.1
Li, M.Y.2
Feng, J.H.3
-
13
-
-
84864917818
-
Development of potent carbonic anhydrase inhibitors incorporating both sulfonamide and sulfamide groups
-
D'Ambrosio K, Smaine F-Z, Carta F, et al. Development of potent carbonic anhydrase inhibitors incorporating both sulfonamide and sulfamide groups. J Med Chem 2012;55:6776-83.
-
(2012)
J Med Chem
, vol.55
, pp. 6776-6783
-
-
D'ambrosio, K.1
Smaine, F.-Z.2
Carta, F.3
-
14
-
-
84872946971
-
The extremo-alpha-carbonic anhydrase (CA) from Sulfurihydrogenibium azorense, the fastest CA known, is highly activated by amino acids and amines
-
Akdemir A, Vullo D, Luca VD, et al. The extremo-alpha-carbonic anhydrase (CA) from Sulfurihydrogenibium azorense, the fastest CA known, is highly activated by amino acids and amines. Bioorg Med Chem Lett 2013;23:1087-90.
-
(2013)
Bioorg Med Chem Lett
, vol.23
, pp. 1087-1090
-
-
Akdemir, A.1
Vullo, D.2
Luca, V.D.3
-
15
-
-
84887843075
-
Synthesis of aminocyanopyrazoles via a multi-component reaction and anticarbonic anhydrase inhibitory activity of their sulfamide derivatives against cytosolic and transmembrane isoforms
-
Allouche F, Chabchoub F, Carta F, Supuran CT. Synthesis of aminocyanopyrazoles via a multi-component reaction and anticarbonic anhydrase inhibitory activity of their sulfamide derivatives against cytosolic and transmembrane isoforms. J Enzym Inhib Med Chem 2013;28:343-9.
-
(2013)
J Enzym Inhib Med Chem
, vol.28
, pp. 343-349
-
-
Allouche, F.1
Chabchoub, F.2
Carta, F.3
Supuran, C.T.4
-
16
-
-
84879037030
-
Secondary/tertiary benzenesulfonamides with inhibitory action against the cytosolic human carbonic anhydrase isoforms i and II
-
Alp C, Maresca A, Alp NA, et al. Secondary/tertiary benzenesulfonamides with inhibitory action against the cytosolic human carbonic anhydrase isoforms I and II. J Enzym Inhib Med Chem 2013;28: 294-8.
-
(2013)
J Enzym Inhib Med Chem
, vol.28
, pp. 294-298
-
-
Alp, C.1
Maresca, A.2
Alp, N.A.3
-
17
-
-
84874626003
-
Dihalogenated sulfanilamides and benzolamides are effective inhibitors of the three beta-class carbonic anhydrases from Mycobacterium tuberculosis
-
Maresca A, Scozzafava A, Vullo D, Supuran CT. Dihalogenated sulfanilamides and benzolamides are effective inhibitors of the three beta-class carbonic anhydrases from Mycobacterium tuberculosis. J Enzym Inhib Med Chem 2013;28:384-7.
-
(2013)
J Enzym Inhib Med Chem
, vol.28
, pp. 384-387
-
-
Maresca, A.1
Scozzafava, A.2
Vullo, D.3
Supuran, C.T.4
-
18
-
-
84890292269
-
Three new aromatic sulfonamide inhibitors of carbonic anhydrases I, II, IV and XII
-
Supuran CT, Maresca A, Gregan F, Remko M. Three new aromatic sulfonamide inhibitors of carbonic anhydrases I, II, IV and XII. J Enzym Inhib Med Chem 2013;28:289-93.
-
(2013)
J Enzym Inhib Med Chem
, vol.28
, pp. 289-293
-
-
Supuran, C.T.1
Maresca, A.2
Gregan, F.3
Remko, M.4
-
19
-
-
84871256917
-
Development of synthetic aminopeptidase N/CD13 inhibitors to overcome cancer metastasis and angiogenesis
-
Su L, Cao J, Jia Y, et al. Development of synthetic aminopeptidase N/CD13 inhibitors to overcome cancer metastasis and angiogenesis. ACS Med Chem Lett 2012;3:959-64.
-
(2012)
ACS Med Chem Lett
, vol.3
, pp. 959-964
-
-
Su, L.1
Cao, J.2
Jia, Y.3
-
20
-
-
77249167010
-
Design, synthesis and preliminary activity assay of 1,2,3,4- tetrahydroisoquinoline-3-carboxylic acid derivatives as novel histone deacetylases (HDACs) inhibitors
-
Zhang YJ, Feng JH, Liu CX, et al. Design, synthesis and preliminary activity assay of 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid derivatives as novel histone deacetylases (HDACs) inhibitors. Bioorg Med Chem 2010;18:1761-72.
-
(2010)
Bioorg Med Chem
, vol.18
, pp. 1761-1772
-
-
Zhang, Y.J.1
Feng, J.H.2
Liu, C.X.3
|