-
1
-
-
0036083396
-
The ubiquitin-proteasome proteolytic pathway: Destruction for the sake of construction
-
Glickman, M. H.; Ciechanover, A. The ubiquitin-proteasome proteolytic pathway: Destruction for the sake of construction Physiol. Rev. 2002, 82, 373-428
-
(2002)
Physiol. Rev.
, vol.82
, pp. 373-428
-
-
Glickman, M.H.1
Ciechanover, A.2
-
3
-
-
0034915764
-
Mechanisms underlying ubiquitination
-
Pickart, C. M. Mechanisms underlying ubiquitination Annu. Rev. Biochem. 2001, 70, 503-533
-
(2001)
Annu. Rev. Biochem.
, vol.70
, pp. 503-533
-
-
Pickart, C.M.1
-
4
-
-
33947659939
-
20S proteasome and its inhibitors: Crystallographic knowledge for drug development
-
Borissenko, L.; Groll, M. 20S proteasome and its inhibitors: crystallographic knowledge for drug development Chem. Rev. 2007, 107, 687-717
-
(2007)
Chem. Rev.
, vol.107
, pp. 687-717
-
-
Borissenko, L.1
Groll, M.2
-
5
-
-
0033197542
-
Proteasome active sites allosterically regulate each other, suggesting a cyclical bite-chew mechanism for protein breakdown
-
Kisselev, A. F.; Akopian, T. N.; Castillo, V.; Goldberg, A. L. Proteasome active sites allosterically regulate each other, suggesting a cyclical bite-chew mechanism for protein breakdown Mol. Cell 1999, 4, 395-402
-
(1999)
Mol. Cell
, vol.4
, pp. 395-402
-
-
Kisselev, A.F.1
Akopian, T.N.2
Castillo, V.3
Goldberg, A.L.4
-
6
-
-
2342667387
-
The development of proteasome inhibitors as anticancer drugs
-
Adams, J. The development of proteasome inhibitors as anticancer drugs Cancer Cell 2004, 5, 417-421
-
(2004)
Cancer Cell
, vol.5
, pp. 417-421
-
-
Adams, J.1
-
7
-
-
20444455939
-
Bortezomib for myeloma - Much ado about something
-
Dispenzieri, A. Bortezomib for myeloma - Much ado about something N. Engl. J. Med. 2005, 352, 2546-2548
-
(2005)
N. Engl. J. Med.
, vol.352
, pp. 2546-2548
-
-
Dispenzieri, A.1
-
8
-
-
33746160660
-
Proteasome inhibitor bortezomib for the treatment of multiple myeloma
-
Cavo, M. Proteasome inhibitor bortezomib for the treatment of multiple myeloma Leukemia 2006, 20, 1341-1352
-
(2006)
Leukemia
, vol.20
, pp. 1341-1352
-
-
Cavo, M.1
-
9
-
-
20444433230
-
Bortezomib or high-dose dexamethasone for relapsed multiple myeloma
-
Richardson, P. G.; Sonneveld, P.; Schuster, M. W.; Irwin, D.; Stadtmauer, E. A.; Facon, T.; Harousseau, J. L.; Yehuda, B. D.; Lonial, S.; Goldschmidt, M. B.; Cavenagh, J.; Dalton, W. S.; Boral, A. L.; Esseltine, D. L.; Porter, J. B.; Schenkein, D.; Anderson, K. C. Bortezomib or high-dose dexamethasone for relapsed multiple myeloma N. Engl. J. Med. 2005, 352, 2487-2498
-
(2005)
N. Engl. J. Med.
, vol.352
, pp. 2487-2498
-
-
Richardson, P.G.1
Sonneveld, P.2
Schuster, M.W.3
Irwin, D.4
Stadtmauer, E.A.5
Facon, T.6
Harousseau, J.L.7
Yehuda, B.D.8
Lonial, S.9
Goldschmidt, M.B.10
Cavenagh, J.11
Dalton, W.S.12
Boral, A.L.13
Esseltine, D.L.14
Porter, J.B.15
Schenkein, D.16
Anderson, K.C.17
-
10
-
-
33644875054
-
Marked clinical activity of the proteasome inhibitor bortezomib in patients with follicular and mantle-cell lymphoma
-
O'Connor, O. A. Marked clinical activity of the proteasome inhibitor bortezomib in patients with follicular and mantle-cell lymphoma Clin. Lymphoma Myeloma 2005, 6, 191-199
-
(2005)
Clin. Lymphoma Myeloma
, vol.6
, pp. 191-199
-
-
O'Connor, O.A.1
-
11
-
-
33750625445
-
Multicenter phase II study of bortezomib in patients with relapsed or refractory mantle cell lymphoma
-
Fisher, R. I.; Bernstein, S. H.; Kahl, B. S.; Djulbegovic, B.; Robertson, M. J.; de Vos, S.; Epner, E.; Krishnan, A.; Leonard, J. P.; Lonial, S.; Stadtmauer, E. A.; O'Connor, O. A.; Shi, H.; Boral, A. L.; Goy, A. Multicenter phase II study of bortezomib in patients with relapsed or refractory mantle cell lymphoma J. Clin. Oncol. 2006, 24, 4867-4874
-
(2006)
J. Clin. Oncol.
, vol.24
, pp. 4867-4874
-
-
Fisher, R.I.1
Bernstein, S.H.2
Kahl, B.S.3
Djulbegovic, B.4
Robertson, M.J.5
De Vos, S.6
Epner, E.7
Krishnan, A.8
Leonard, J.P.9
Lonial, S.10
Stadtmauer, E.A.11
O'Connor, O.A.12
Shi, H.13
Boral, A.L.14
Goy, A.15
-
12
-
-
0037973279
-
A phase 2 study of bortezomib in relapsed, refractory myeloma
-
Richardson, P. G.; Barlogie, B.; Berenson, J.; Singhal, S.; Jagannath, S.; Irwin, D.; Rajkumar, S. V.; Srkalovic, G.; Alsina, M.; Alexanian, R.; Siegel, D.; Orlowski, R. Z.; Kuter, D.; Limentani, S. A.; Lee, S.; Hideshima, T.; Esseltine, D. L.; Kauffman, M.; Adams, J.; Schenkein, D. P.; Anderson, K. C. A phase 2 study of bortezomib in relapsed, refractory myeloma N. Engl. J. Med. 2003, 348, 2609-2617
-
(2003)
N. Engl. J. Med.
, vol.348
, pp. 2609-2617
-
-
Richardson, P.G.1
Barlogie, B.2
Berenson, J.3
Singhal, S.4
Jagannath, S.5
Irwin, D.6
Rajkumar, S.V.7
Srkalovic, G.8
Alsina, M.9
Alexanian, R.10
Siegel, D.11
Orlowski, R.Z.12
Kuter, D.13
Limentani, S.A.14
Lee, S.15
Hideshima, T.16
Esseltine, D.L.17
Kauffman, M.18
Adams, J.19
Schenkein, D.P.20
Anderson, K.C.21
more..
-
13
-
-
27244460815
-
Proteasome inhibition and its clinical prospects in the treatment of hematologic and solid malignancies
-
Ludwig, H.; Khayat, D.; Giaccone, G.; Facon, T. Proteasome inhibition and its clinical prospects in the treatment of hematologic and solid malignancies Cancer 2005, 104, 1794-1807
-
(2005)
Cancer
, vol.104
, pp. 1794-1807
-
-
Ludwig, H.1
Khayat, D.2
Giaccone, G.3
Facon, T.4
-
14
-
-
67650754085
-
Design, synthesis, biological evaluation, and structure-activity relationship (SAR) discussion of dipeptidyl boronate proteasome inhibitors, part I: Comprehensive understanding of the SAR of α -amino acid boronates
-
Zhu, Y. Q.; Zhao, X.; Zhu, X. R; Wu, G.; Li, Y. J.; Ma, Y. H.; Yuan, Y. X.; Yang, J.; Hu, Y.; Ai, L.; Gao, Q. Z. Design, synthesis, biological evaluation, and structure-activity relationship (SAR) discussion of dipeptidyl boronate proteasome inhibitors, part I: Comprehensive understanding of the SAR of α -amino acid boronates J. Med. Chem. 2009, 52, 4192-4199
-
(2009)
J. Med. Chem.
, vol.52
, pp. 4192-4199
-
-
Zhu, Y.Q.1
Zhao, X.2
Zhu, X.R.3
Wu, G.4
Li, Y.J.5
Ma, Y.H.6
Yuan, Y.X.7
Yang, J.8
Hu, Y.9
Ai, L.10
Gao, Q.Z.11
-
15
-
-
69949163678
-
Design, synthesis and biological evaluation of tripeptide boronic acid proteasome inhibitors
-
Zhu, Y. Q.; Yao, S. Y; Xu, B.; Ge, Z. M.; Cui, J. R.; Chen, T. M.; Li, R. T. Design, synthesis and biological evaluation of tripeptide boronic acid proteasome inhibitors Bioorg. Med. Chem. 2009, 17, 6851-6861
-
(2009)
Bioorg. Med. Chem.
, vol.17
, pp. 6851-6861
-
-
Zhu, Y.Q.1
Yao, S.Y.2
Xu, B.3
Ge, Z.M.4
Cui, J.R.5
Chen, T.M.6
Li, R.T.7
-
16
-
-
14844312173
-
Asymmetric synthesis of β-amino acids and α-substituted β-amino acids
-
Cardillo, G.; Tomasini, C. Asymmetric synthesis of β-amino acids and α-substituted β-amino acids Chem. Soc. Rev. 1996, 25, 117-128
-
(1996)
Chem. Soc. Rev.
, vol.25
, pp. 117-128
-
-
Cardillo, G.1
Tomasini, C.2
-
17
-
-
3242870662
-
The conquest of Taxol
-
Nicolaou, K. C.; Guy, R. K. The conquest of Taxol Angew. Chem., Int. Ed. Engl. 1995, 34, 2079-2090
-
(1995)
Angew. Chem., Int. Ed. Engl.
, vol.34
, pp. 2079-2090
-
-
Nicolaou, K.C.1
Guy, R.K.2
-
18
-
-
0023238523
-
Chemistry of emeriamine and its analogs and their inhibitory activity in long-chain fatty acid oxidation
-
Shinagawa, S.; Kanamaru, T.; Harada, S.; Asai, M.; Okazaki, H. Chemistry of emeriamine and its analogs and their inhibitory activity in long-chain fatty acid oxidation J. Med. Chem. 1987, 30, 1458-1463
-
(1987)
J. Med. Chem.
, vol.30
, pp. 1458-1463
-
-
Shinagawa, S.1
Kanamaru, T.2
Harada, S.3
Asai, M.4
Okazaki, H.5
-
19
-
-
0033618140
-
HIV-inhibitory and cytotoxic depsipeptides from the sponge theonella mirabilis and theonella swinhoei collected in Papua new Guinea
-
Ford, P. W.; Gustafson, K. R.; McKee, T. C.; Shigematsu, N.; Maurizi, L. K.; Pannell, L. K.; Williams, D. E.; de Silva, E. D.; Lassota, P.; Allen, T. M.; Van Soest, R.; Andersen, R. J.; Boyd, M. R.; Papuamides, A-D HIV-inhibitory and cytotoxic depsipeptides from the sponge theonella mirabilis and theonella swinhoei collected in Papua new Guinea J. Am. Chem. Soc. 1999, 121, 5899-5909
-
(1999)
J. Am. Chem. Soc.
, vol.121
, pp. 5899-5909
-
-
Ford, P.W.1
Gustafson, K.R.2
McKee, T.C.3
Shigematsu, N.4
Maurizi, L.K.5
Pannell, L.K.6
Williams, D.E.7
De Silva, E.D.8
Lassota, P.9
Allen, T.M.10
Van Soest, R.11
Andersen, R.J.12
Boyd, M.R.13
Papuamides, A.-D.14
-
20
-
-
0015211527
-
Plant Antitumor Agents. VI. The isolation and structure of Taxol, a novel antileukemic and antitumor agent from Taxus brevifolia
-
Wani, M. C.; Taylor, H. L.; Wall, M. E.; Coggon, P.; McPhail, A. T. Plant Antitumor Agents. VI. The isolation and structure of Taxol, a novel antileukemic and antitumor agent from Taxus brevifolia J. Am. Chem. Soc. 1971, 93, 2325-2327
-
(1971)
J. Am. Chem. Soc.
, vol.93
, pp. 2325-2327
-
-
Wani, M.C.1
Taylor, H.L.2
Wall, M.E.3
Coggon, P.4
McPhail, A.T.5
-
21
-
-
0013926298
-
On the chemical nature of the antibiotic edeine
-
Roncari, G.; Kurylo-Borowska, Z.; Craig, L. C. On the chemical nature of the antibiotic edeine Biochemistry 1966, 5, 2153-2159
-
(1966)
Biochemistry
, vol.5
, pp. 2153-2159
-
-
Roncari, G.1
Kurylo-Borowska, Z.2
Craig, L.C.3
-
22
-
-
0019815526
-
Studies of nitrogen metabolism using C-13 NMR spectroscopy. 3. Synthesis of DL-[3-13C, 2-15N]lysine and its incorporation into streptothricin F1
-
Gould, S. J.; Thiruvengadam, T. K. Studies of nitrogen metabolism using C-13 NMR spectroscopy. 3. Synthesis of DL-[3-13C, 2-15N]lysine and its incorporation into streptothricin F1 J. Am. Chem. Soc. 1981, 103, 6752-6754
-
(1981)
J. Am. Chem. Soc.
, vol.103
, pp. 6752-6754
-
-
Gould, S.J.1
Thiruvengadam, T.K.2
-
23
-
-
0000466569
-
The biological stability of β-peptides: No interactions between α- And β-peptidic structures?
-
Hinterman, T.; Seebach, D. The biological stability of β-peptides: No interactions between α- and β-peptidic structures? Chimia 1997, 51, 244-247
-
(1997)
Chimia
, vol.51
, pp. 244-247
-
-
Hinterman, T.1
Seebach, D.2
-
24
-
-
77949367260
-
Synthesis, in vitro and in vivo biological evaluation, docking studies and structure-activity relationship (SAR) discussion of dipeptidyl boronic acid proteasome inhibitors composed of β-amino acids
-
Zhu, Y. Q.; Zhu, X. R.; Wu, G.; Ma, Y. H.; Li, Y. J.; Zhao, X.; Yuan, Y. X.; Yang, J.; Yu, S.; Shao, F.; Li, R. T.; Ke, Y. R.; Lu, A. J.; Liu, Z. M.; Zhang, L. R. Synthesis, in vitro and in vivo biological evaluation, docking studies and structure-activity relationship (SAR) discussion of dipeptidyl boronic acid proteasome inhibitors composed of β-amino acids J. Med. Chem. 2010, 53, 1990-1999
-
(2010)
J. Med. Chem.
, vol.53
, pp. 1990-1999
-
-
Zhu, Y.Q.1
Zhu, X.R.2
Wu, G.3
Ma, Y.H.4
Li, Y.J.5
Zhao, X.6
Yuan, Y.X.7
Yang, J.8
Yu, S.9
Shao, F.10
Li, R.T.11
Ke, Y.R.12
Lu, A.J.13
Liu, Z.M.14
Zhang, L.R.15
-
25
-
-
85004737474
-
Coupling reagents in peptide synthesis
-
Klausner, Y. S.; Bodansky, M. Coupling reagents in peptide synthesis Synthesis 1972, 453-463
-
(1972)
Synthesis
, pp. 453-463
-
-
Klausner, Y.S.1
Bodansky, M.2
-
26
-
-
13044316560
-
Role of the proteasome and NF-kappa B in streptoccal cell wall-induced polyarthritis
-
Pallombella, V. J.; Conner, E. M.; Fuseler, J. W.; Destree, A.; Davis, J. M.; Laroux, F. S.; Wolf, R. E.; Huang, J.; Brand, S.; Elliott, P. J.; Lazarus, D.; Parent, L.; Stein, R.; Adams, J.; Grisham, M. B. Role of the proteasome and NF-kappa B in streptoccal cell wall-induced polyarthritis Proc. Natl. Acad. Sci. U.S.A. 1998, 95, 15671-15676
-
(1998)
Proc. Natl. Acad. Sci. U.S.A.
, vol.95
, pp. 15671-15676
-
-
Pallombella, V.J.1
Conner, E.M.2
Fuseler, J.W.3
Destree, A.4
Davis, J.M.5
Laroux, F.S.6
Wolf, R.E.7
Huang, J.8
Brand, S.9
Elliott, P.J.10
Lazarus, D.11
Parent, L.12
Stein, R.13
Adams, J.14
Grisham, M.B.15
-
27
-
-
0032885416
-
The proteasome inhibitor PS-341 in cancer therapy
-
Teicher, B. A.; Ara, G.; Herbst, R.; Palombella, V. J.; Adams, J. The proteasome inhibitor PS-341 in cancer therapy Clin. Cancer Res. 1999, 5, 2638-2645
-
(1999)
Clin. Cancer Res.
, vol.5
, pp. 2638-2645
-
-
Teicher, B.A.1
Ara, G.2
Herbst, R.3
Palombella, V.J.4
Adams, J.5
|