-
1
-
-
33947659939
-
20S Proteasome and its inhibitors: Crystallographic knowledge for drug development
-
L. Borissenko, and M. Groll 20S Proteasome and its inhibitors: crystallographic knowledge for drug development Chem. Rev. 107 2007 687 717
-
(2007)
Chem. Rev.
, vol.107
, pp. 687-717
-
-
Borissenko, L.1
Groll, M.2
-
2
-
-
80051978811
-
The predator becomes the prey: Regulating the ubiquitin system by ubiquitylation and degradation
-
A.M. Weissman, N. Shabek, and A. Ciechanover The predator becomes the prey: regulating the ubiquitin system by ubiquitylation and degradation Nat. Rev. Mol. Cell Biol. 12 2011 605 620
-
(2011)
Nat. Rev. Mol. Cell Biol.
, vol.12
, pp. 605-620
-
-
Weissman, A.M.1
Shabek, N.2
Ciechanover, A.3
-
3
-
-
84860225255
-
Intracellular protein degradation: From a vague idea through the lysosome and the ubiquitin-proteasome system and onto human diseases and drug targeting
-
A. Ciechanover Intracellular protein degradation: from a vague idea through the lysosome and the ubiquitin-proteasome system and onto human diseases and drug targeting Neurodegener. Dis. 10 2012 7 22
-
(2012)
Neurodegener. Dis.
, vol.10
, pp. 7-22
-
-
Ciechanover, A.1
-
5
-
-
34848870352
-
Bortezomib for the treatment of mantle cell lymphoma
-
R.C. Kane, R. Dagher, A. Farrell, C.W. Ko, R. Sridhara, R. Justice, and R. Pazdur Bortezomib for the treatment of mantle cell lymphoma Clin. Cancer Res. 13 2007 5291 5294
-
(2007)
Clin. Cancer Res.
, vol.13
, pp. 5291-5294
-
-
Kane, R.C.1
Dagher, R.2
Farrell, A.3
Ko, C.W.4
Sridhara, R.5
Justice, R.6
Pazdur, R.7
-
6
-
-
0027423502
-
Concepts and progress in the development of peptide mimetics
-
G.L. Olson, D.R. Bolin, M.P. Bonner, M. Bös, C.M. Cook, D.C. Fry, B.J. Graves, M. Hatada, D.E. Hill, M. Kahn, V.S. Madison, V.K. Rusiecki, R. Sarabu, J. Sepinwall, G.P. Vincent, and M.E. Voss Concepts and progress in the development of peptide mimetics J. Med. Chem. 36 1993 3039 3049
-
(1993)
J. Med. Chem.
, vol.36
, pp. 3039-3049
-
-
Olson, G.L.1
Bolin, D.R.2
Bonner, M.P.3
Bös, M.4
Cook, C.M.5
Fry, D.C.6
Graves, B.J.7
Hatada, M.8
Hill, D.E.9
Kahn, M.10
Madison, V.S.11
Rusiecki, V.K.12
Sarabu, R.13
Sepinwall, J.14
Vincent, G.P.15
Voss, M.E.16
-
7
-
-
33644845743
-
Crystal structure of the boronic acid-based proteasome inhibitor bortezomib in complex with the yeast 20S proteasome
-
M. Groll, C.R. Berkers, H.L. Ploegh, and H. Ovaa Crystal structure of the boronic acid-based proteasome inhibitor bortezomib in complex with the yeast 20S proteasome Structure 14 2006 451 456
-
(2006)
Structure
, vol.14
, pp. 451-456
-
-
Groll, M.1
Berkers, C.R.2
Ploegh, H.L.3
Ovaa, H.4
-
8
-
-
34249033946
-
A general strategy for the synthesis of amino-substituted 2-pyridones using a palladium-catalyzed amination reaction
-
Y.H. Kim, Y. Kim, S. Chang, B. Kim, and J. Heo A general strategy for the synthesis of amino-substituted 2-pyridones using a palladium-catalyzed amination reaction Bull. Korean Chem. Soc. 28 2007 777 782
-
(2007)
Bull. Korean Chem. Soc.
, vol.28
, pp. 777-782
-
-
Kim, Y.H.1
Kim, Y.2
Chang, S.3
Kim, B.4
Heo, J.5
-
9
-
-
0000793111
-
Synthesis and properties of pinanediol α-amido boronic esters
-
D.S. Matteson, P.K. Jesthi, and K.M. Sadhu Synthesis and properties of pinanediol α-amido boronic esters Organometallics 3 1984 1284 1288
-
(1984)
Organometallics
, vol.3
, pp. 1284-1288
-
-
Matteson, D.S.1
Jesthi, P.K.2
Sadhu, K.M.3
-
10
-
-
33750933092
-
Ready access to 7,8-dihydro- and 1,2,3,4-tetrahydro-1,6-naphthyridine- 5(6H)-ones from simple pyridine precursors
-
H.D.H. Showalter Ready access to 7,8-dihydro- and 1,2,3,4-tetrahydro-1,6- naphthyridine-5(6H)-ones from simple pyridine precursors J. Heterocycl. Chem. 43 2006 1311 1317
-
(2006)
J. Heterocycl. Chem.
, vol.43
, pp. 1311-1317
-
-
Showalter, H.D.H.1
-
11
-
-
0033152760
-
Proteasome inhibitors: A novel class of potent and effective antitumor agents
-
J. Adams, V.J. Palombella, E.A. Sausville, J. Johnson, A. Destree, D.D. Lazarus, J. Maas, C.S. Pien, S. Prakash, and P.J. Elliott Proteasome inhibitors: a novel class of potent and effective antitumor agents Cancer Res. 59 1999 2615 2622
-
(1999)
Cancer Res.
, vol.59
, pp. 2615-2622
-
-
Adams, J.1
Palombella, V.J.2
Sausville, E.A.3
Johnson, J.4
Destree, A.5
Lazarus, D.D.6
Maas, J.7
Pien, C.S.8
Prakash, S.9
Elliott, P.J.10
-
12
-
-
33646841837
-
Importance of different active sites in protein breakdown by 26S proteasomes and the efficacy of proteasome inhibitors varies with the protein substrate
-
A.F. Kisselev, A. Callard, and A.L. Goldberg Importance of different active sites in protein breakdown by 26S proteasomes and the efficacy of proteasome inhibitors varies with the protein substrate J. Biol. Chem. 281 2006 8582 8590
-
(2006)
J. Biol. Chem.
, vol.281
, pp. 8582-8590
-
-
Kisselev, A.F.1
Callard, A.2
Goldberg, A.L.3
-
13
-
-
73149103209
-
Selective inhibitor of proteasome's caspase-like sites sensitises cells to specific inhibition of chymotripsin-like sites
-
M. Britton, M.M. Lucas, S.L. Downey, M. Screen, A.A. Pletnev, M. Verdoes, R.A. Tokhunts, O. Amir, A.L. Goddard, P.M. Pelphrey, D.L. Wright, H.S. OverKleeft, and A.F. Kisselev Selective inhibitor of proteasome's caspase-like sites sensitises cells to specific inhibition of chymotripsin-like sites Chem. Biol. 16 2009 1278 1289
-
(2009)
Chem. Biol.
, vol.16
, pp. 1278-1289
-
-
Britton, M.1
Lucas, M.M.2
Downey, S.L.3
Screen, M.4
Pletnev, A.A.5
Verdoes, M.6
Tokhunts, R.A.7
Amir, O.8
Goddard, A.L.9
Pelphrey, P.M.10
Wright, D.L.11
Overkleeft, H.S.12
Kisselev, A.F.13
-
14
-
-
70350708810
-
Carfilzomib can induce tumor cell death through selective inhibition of the chymotrypsin-like activity of the proteasome
-
F. Parlati, S.J. Lee, M. Aujay, E. Suzuk, K. Levitsky, J.B. Lorens, D.R. Micklem, P. Ruurs, C. Sylvain, Y. Lu, K.D. Shenk, and M.K. Bennett Carfilzomib can induce tumor cell death through selective inhibition of the chymotrypsin-like activity of the proteasome Blood 114 2009 3439 3447
-
(2009)
Blood
, vol.114
, pp. 3439-3447
-
-
Parlati, F.1
Lee, S.J.2
Aujay, M.3
Suzuk, E.4
Levitsky, K.5
Lorens, J.B.6
Micklem, D.R.7
Ruurs, P.8
Sylvain, C.9
Lu, Y.10
Shenk, K.D.11
Bennett, M.K.12
-
15
-
-
0031552362
-
Development and validation of a genetic algorithm for flexible docking
-
G. Jones, P. Willett, R.C. Glen, A.R. Leach, and R. Taylor Development and validation of a genetic algorithm for flexible docking J. Mol. Biol. 267 1997 727 748
-
(1997)
J. Mol. Biol.
, vol.267
, pp. 727-748
-
-
Jones, G.1
Willett, P.2
Glen, R.C.3
Leach, A.R.4
Taylor, R.5
-
16
-
-
84875060651
-
-
The Cambridge Crystallographic Data Centre Cambridge, U.K.
-
GOLD, Version 5.1 2012 The Cambridge Crystallographic Data Centre Cambridge, U.K.
-
(2012)
GOLD, Version 5.1
-
-
-
17
-
-
0041919542
-
Improved protein-ligand docking using GOLD
-
M.L. Verdonk, J.C. Cole, M.J. Hartshorn, C.W. Murray, and R.D. Taylor Improved protein-ligand docking using GOLD Proteins: Struct. Funct. Genet. 52 2003 609 623
-
(2003)
Proteins: Struct. Funct. Genet.
, vol.52
, pp. 609-623
-
-
Verdonk, M.L.1
Cole, J.C.2
Hartshorn, M.J.3
Murray, C.W.4
Taylor, R.D.5
-
18
-
-
70350041556
-
New 2-aryloxy-3-phenyl-propanoic acids as PPAR α/γ dual agonists with improved potency and reduced adverse effects on skeletal muscle function
-
G. Fracchiolla, A. Laghezza, L. Piemontese, P. Tortorella, F. Mazza, R. Montanari, G. Pochetti, A. Lavecchia, E. Novellino, S. Pierno, D. Conte Camerino, and F. Loiodice New 2-aryloxy-3-phenyl-propanoic acids as PPAR α/γ dual agonists with improved potency and reduced adverse effects on skeletal muscle function J. Med. Chem. 52 2009 6382 6393
-
(2009)
J. Med. Chem.
, vol.52
, pp. 6382-6393
-
-
Fracchiolla, G.1
Laghezza, A.2
Piemontese, L.3
Tortorella, P.4
Mazza, F.5
Montanari, R.6
Pochetti, G.7
Lavecchia, A.8
Novellino, E.9
Pierno, S.10
Conte Camerino, D.11
Loiodice, F.12
-
19
-
-
64349101279
-
Exploiting the pyrazolo[3,4-d]pyrimidin-4-one ring system as a useful template to obtain potent adenosine deaminase inhibitors
-
C. La Motta, S. Sartini, L. Mugnaini, S. Salerno, F. Simorini, S. Taliani, A.M. Marini, F. Da Settimo, A. Lavecchia, E. Novellino, L. Antonioli, M. Fornai, C. Blandizzi, and M. Del Tacca Exploiting the pyrazolo[3,4-d] pyrimidin-4-one ring system as a useful template to obtain potent adenosine deaminase inhibitors J. Med. Chem. 52 2009 1681 1692
-
(2009)
J. Med. Chem.
, vol.52
, pp. 1681-1692
-
-
La Motta, C.1
Sartini, S.2
Mugnaini, L.3
Salerno, S.4
Simorini, F.5
Taliani, S.6
Marini, A.M.7
Da Settimo, F.8
Lavecchia, A.9
Novellino, E.10
Antonioli, L.11
Fornai, M.12
Blandizzi, C.13
Del Tacca, M.14
-
20
-
-
84855839232
-
Synthesis, characterization and biological evaluation of ureidofibrate-like derivatives endowed with peroxisome proliferator-activated receptor activity
-
L. Porcelli, F. Gilardi, A. Laghezza, L. Piemontese, N. Mitro, A. Azzariti, F. Altieri, L. Cervoni, G. Fracchiolla, M. Giudici, U. Guerrini, A. Lavecchia, R. Montanari, C. Di Giovanni, A. Paradiso, G. Pochetti, G.M. Simone, P. Tortorella, M. Crestani, and F. Loiodice Synthesis, characterization and biological evaluation of ureidofibrate-like derivatives endowed with peroxisome proliferator-activated receptor activity J. Med. Chem. 55 2012 37 54
-
(2012)
J. Med. Chem.
, vol.55
, pp. 37-54
-
-
Porcelli, L.1
Gilardi, F.2
Laghezza, A.3
Piemontese, L.4
Mitro, N.5
Azzariti, A.6
Altieri, F.7
Cervoni, L.8
Fracchiolla, G.9
Giudici, M.10
Guerrini, U.11
Lavecchia, A.12
Montanari, R.13
Di Giovanni, C.14
Paradiso, A.15
Pochetti, G.16
Simone, G.M.17
Tortorella, P.18
Crestani, M.19
Loiodice, F.20
more..
-
21
-
-
84859199887
-
Core ring nature in diarylheterocycle COX-1 inhibitors
-
M.G. Perrone, P. Vitale, P. Malerba, A. Altomare, A. Lavecchia, C. Di Giovanni, E. Novellino, and A. Scilimati Core ring nature in diarylheterocycle COX-1 inhibitors Chem. Med. Chem. 7 2012 629 641
-
(2012)
Chem. Med. Chem.
, vol.7
, pp. 629-641
-
-
Perrone, M.G.1
Vitale, P.2
Malerba, P.3
Altomare, A.4
Lavecchia, A.5
Di Giovanni, C.6
Novellino, E.7
Scilimati, A.8
-
22
-
-
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
-
Y.Q. Zhu, X. Zhao, X.R. Zhu, G. Wu, Y.J. Li, Y.H. Ma, Y.X. Yuan, J. Yang, Y. Hu, L. Ai, and Q.Z. Gao 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. 52 2009 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
-
23
-
-
33646753668
-
Optimization of subsite binding to the 5 subunit of the human 20S proteasome using vinyl sulfones and 2-keto-1, 3, 4-oxadiazoles: Syntheses and cellular properties of potent, selective proteasome inhibitors
-
R.M. Rydzewski, L. Burrill, R. Mendonca, J.T. Palmer, M. Rice, R. Tahilramani, K.E. Bass, L. Leung, E. Gjerstad, J.W. Janc, and L. Pan Optimization of subsite binding to the 5 subunit of the human 20S proteasome using vinyl sulfones and 2-keto-1, 3, 4-oxadiazoles: syntheses and cellular properties of potent, selective proteasome inhibitors J. Med. Chem. 49 2006 2953 2968
-
(2006)
J. Med. Chem.
, vol.49
, pp. 2953-2968
-
-
Rydzewski, R.M.1
Burrill, L.2
Mendonca, R.3
Palmer, J.T.4
Rice, M.5
Tahilramani, R.6
Bass, K.E.7
Leung, L.8
Gjerstad, E.9
Janc, J.W.10
Pan, L.11
-
24
-
-
80053555768
-
Strength and character of halogen bonds in protein-ligand complexes
-
K.E. Riley, and P.J. Hobza Strength and character of halogen bonds in protein-ligand complexes Cryst. Growth Des. 11 2011 4272 4278
-
(2011)
Cryst. Growth Des.
, vol.11
, pp. 4272-4278
-
-
Riley, K.E.1
Hobza, P.J.2
-
26
-
-
84879106434
-
Preparation of 2-hydroxypyridines and 2-(1H)-pyridones by hydrogenation of aralkyloxypyridines
-
JP 09059254 A2
-
A. Terajima, T. Kajashiki, and T. Kato Preparation of 2-hydroxypyridines and 2-(1H)-pyridones by hydrogenation of aralkyloxypyridines Jpn. Kokai Tokkyo Koho 4 March 1997 JP 09059254 A2
-
(1997)
Jpn. Kokai Tokkyo Koho
-
-
Terajima, A.1
Kajashiki, T.2
Kato, T.3
-
27
-
-
27744564578
-
Design and synthesis of aromatic inhibitors of anthranilate synthase
-
R.J. Payne, E.M.M. Bulloch, A.D. Abell, and C. Abell Design and synthesis of aromatic inhibitors of anthranilate synthase Org. Biomol. Chem. 3 2005 3629 3635
-
(2005)
Org. Biomol. Chem.
, vol.3
, pp. 3629-3635
-
-
Payne, R.J.1
Bulloch, E.M.M.2
Abell, A.D.3
Abell, C.4
-
28
-
-
80054956766
-
-
Schrödinger, LLC New York, NY
-
Maestro, Version 9.2 2011 Schrödinger, LLC New York, NY
-
(2011)
Maestro, Version 9.2
-
-
-
29
-
-
0000577528
-
Chimera: An extensible molecular modelling application constructed using standard components
-
C.C. Huang, G.S. Couch, E.F. Pettersen, and T.E. Ferrin Chimera: an extensible molecular modelling application constructed using standard components Pacif. Symp. Biocomput. 1 1996 724 http://www.cgl.ucsf.edu/chimera
-
(1996)
Pacif. Symp. Biocomput.
, vol.1
, pp. 724
-
-
Huang, C.C.1
Couch, G.S.2
Pettersen, E.F.3
Ferrin, T.E.4
-
30
-
-
0003845223
-
-
DeLano Scientific LLC, San Carlos, CA, USA
-
W.L. DeLano, The PyMOL Molecular Graphics System, DeLano Scientific LLC, San Carlos, CA, USA, http://www.pymol.org/. della Ricerca Scientifica e Tecnologica
-
The PyMOL Molecular Graphics System
-
-
Delano, W.L.1
|