-
1
-
-
0034020466
-
-
(a) Cheung, W. L.; Briggs, S. D.; Allis, C. D. Curr. Opin. Cell Biol. 2000, 12, 326
-
(2000)
Curr. Opin. Cell Biol.
, vol.12
, pp. 326
-
-
Cheung, W.L.1
Briggs, S.D.2
Allis, C.D.3
-
5
-
-
0035917474
-
-
(b) For a discussion of the SIRT active site, see: Dutnall R.N., Pillus L. Cell. 105:2001;161.
-
(2001)
Cell
, vol.105
, pp. 161
-
-
Dutnall, R.N.1
Pillus, L.2
-
6
-
-
0037016696
-
-
For the most recent published isolation (HDAC 10), see: Kao H.Y., Lee C.H., Komarov A., Han C.C., Evans R.M. J. Biol. Chem. 277:2002;187.
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 187
-
-
Kao, H.Y.1
Lee, C.H.2
Komarov, A.3
Han, C.C.4
Evans, R.M.5
-
9
-
-
0032539890
-
-
50 was determined using immunoprecipitated HDAC1. Richon V.M., Emiliani S., Verdin E., Webb Y., Breslow R., Rifkind R.A., Marks P.A. Proc. Natl. Acad. Sci. U.S.A. 95:1998;3003.
-
(1998)
Proc. Natl. Acad. Sci. U.S.A.
, vol.95
, pp. 3003
-
-
Richon, V.M.1
Emiliani, S.2
Verdin, E.3
Webb, Y.4
Breslow, R.5
Rifkind, R.A.6
Marks, P.A.7
-
10
-
-
0027378351
-
-
50 was determined in ref 8 against recombinant HDAC1. Kijima M., Yoshida M., Sugita K., Horinouchi S., Beppu T. J. Biol. Chem. 268:1993;22429.
-
(1993)
J. Biol. Chem.
, vol.268
, pp. 22429
-
-
Kijima, M.1
Yoshida, M.2
Sugita, K.3
Horinouchi, S.4
Beppu, T.5
-
11
-
-
0035793107
-
-
50 was determined using recombinant HDAC1. Furumai R., Komatsu Y., Nishino N., Khochbin S., Yoshida M., Horinouchi S. Proc. Natl. Acad. Sci. U.S.A. 98:2001;87.
-
(2001)
Proc. Natl. Acad. Sci. U.S.A.
, vol.98
, pp. 87
-
-
Furumai, R.1
Komatsu, Y.2
Nishino, N.3
Khochbin, S.4
Yoshida, M.5
Horinouchi, S.6
-
12
-
-
0011115960
-
-
note
-
18
-
-
-
-
13
-
-
0030744926
-
-
(b) Compound 4 is similar to inhibitors reported in: Jung M.; Hoffmann, K.; Brosch, G.; Loidl, P. Bioorg. Med. Chem. Lett. 1997, 7, 1655.
-
(1997)
Bioorg. Med. Chem. Lett.
, vol.7
, pp. 1655
-
-
Jung, M.1
Hoffmann, K.2
Brosch, G.3
Loidl, P.4
-
15
-
-
0033523895
-
-
(b) Jung M., Gerald B., Kolle D., Scherf H., Gerhauser C., Loidl P. J. Med. Chem. 42:1999;4669.
-
(1999)
J. Med. Chem.
, vol.42
, pp. 4669
-
-
Jung, M.1
Gerald, B.2
Kolle, D.3
Scherf, H.4
Gerhauser, C.5
Loidl, P.6
-
16
-
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0032544135
-
-
Steinman D.H., Curtin M.L., Garland R.B., Davidsen S.K., Heyman R.H., Holms J.H., Albert D.H., Magoc T.J., Nagy I.B., Marcotte P.A., Li J., Morgan D.W., Hutchins C., Summers J.B. Bioorg. Med. Chem. Lett. 8:1998;2087.
-
(1998)
Bioorg. Med. Chem. Lett.
, vol.8
, pp. 2087
-
-
Steinman, D.H.1
Curtin, M.L.2
Garland, R.B.3
Davidsen, S.K.4
Heyman, R.H.5
Holms, J.H.6
Albert, D.H.7
Magoc, T.J.8
Nagy, I.B.9
Marcotte, P.A.10
Li, J.11
Morgan, D.W.12
Hutchins, C.13
Summers, J.B.14
-
17
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0011110949
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note
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1H NMR, mass spectroscopy and elemental analysis.
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18
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0011153113
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An X-ray crystal structure was obtained of carboxylic acid 9, which was isolated in low yield from a macrocycle synthetic route similar to that shown in Scheme 4 . Carboxylic acid 9 was coupled with amine 10 and the product was debenzylated to give authentic hydroxamic acid 6.
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19
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0022600858
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Cyclizations of succinamide esters under basic conditions have been reported but only for acyclic systems with unhindered esters (i.e., methyl, benzyl). For an example, see: Fujii N., Nomizu M., Futaki S., Otaka A., Funakoshi S., Akaji K., Watanabe K., Yajima H. Chem. Pharm. Bull. 34:1986;864.
-
(1986)
Chem. Pharm. Bull.
, vol.34
, pp. 864
-
-
Fujii, N.1
Nomizu, M.2
Futaki, S.3
Otaka, A.4
Funakoshi, S.5
Akaji, K.6
Watanabe, K.7
Yajima, H.8
-
22
-
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0032537578
-
-
Curtin M.L., Garland R.B., Davidsen S.K., Marcotte P.A., Albert D.H., Magoc T.J., Hutchins C. Bioorg. Med. Chem. Lett. 8:1998;1443.
-
(1998)
Bioorg. Med. Chem. Lett.
, vol.8
, pp. 1443
-
-
Curtin, M.L.1
Garland, R.B.2
Davidsen, S.K.3
Marcotte, P.A.4
Albert, D.H.5
Magoc, T.J.6
Hutchins, C.7
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24
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0011078958
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note
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max fluorescence plate reader (Molecular Devices, San Diego, CA, USA). Treated cells were compared to vehicle treated cells to determine growth inhibition.
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25
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0011153114
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note
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(a) Hyperacetylation of histone H4 was induced in T24 bladder carcinoma cells after 4 h exposure to HDAC inhibitors. Hyperacetylated histone H4 was analyzed by Western blot using an anti-acetylated H4 antibody (UBI, Lake Placid, NY) and 5 μg/lane of acid-extracted nuclear histones
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26
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0011153320
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note
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waf1/cip1 monoclonal antibody (UBI) and 100 μg/lane of cellular lysate.
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27
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0033520944
-
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Sambucetti L.C., Fischer D.D., Zabludoff S., Kwon P.O., Chamberlin H., Trogani N., Xu H., Cohen D. J. Biol. Chem. 274:1999;34940.
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 34940
-
-
Sambucetti, L.C.1
Fischer, D.D.2
Zabludoff, S.3
Kwon, P.O.4
Chamberlin, H.5
Trogani, N.6
Xu, H.7
Cohen, D.8
-
28
-
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0033539092
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-
Finnin M.S., Donigian J.R., Cohen A., Richon V.M., Rifkind R.A., Marks P.A., Breslow R., Pavletich N.P. Nature. 401:1999;188.
-
(1999)
Nature
, vol.401
, pp. 188
-
-
Finnin, M.S.1
Donigian, J.R.2
Cohen, A.3
Richon, V.M.4
Rifkind, R.A.5
Marks, P.A.6
Breslow, R.7
Pavletich, N.P.8
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