-
1
-
-
84979097462
-
Metalloprotein Inhibitors for the Treatment of Human Diseases
-
Yang, Y.; Hu, X.-Q.; Li, Q.-S.; Zhang, X.-X.; Ruan, B.-F.; Xu, J.; Liao, C. Metalloprotein Inhibitors for the Treatment of Human Diseases Curr. Top. Med. Chem. 2016, 16, 384-396 10.2174/1568026615666150813145218
-
(2016)
Curr. Top. Med. Chem.
, vol.16
, pp. 384-396
-
-
Yang, Y.1
Hu, X.-Q.2
Li, Q.-S.3
Zhang, X.-X.4
Ruan, B.-F.5
Xu, J.6
Liao, C.7
-
2
-
-
84906871164
-
Metalloprotein Inhibitors
-
Storr, T. John Wiley & Sons, Ltd: United Kingdom
-
Martin, D. P.; Puerta, D. T.; Cohen, S. M. Metalloprotein Inhibitors. In Ligand Design in Medicinal Inorganic Chemistry; Storr, T., Ed.; John Wiley & Sons, Ltd: United Kingdom, 2014; pp 375-404.
-
(2014)
Ligand Design in Medicinal Inorganic Chemistry
, pp. 375-404
-
-
Martin, D.P.1
Puerta, D.T.2
Cohen, S.M.3
-
3
-
-
0001651169
-
Design and therapeutic application of matrix metalloproteinase inhibitors
-
Whittaker, M.; Floyd, C. D.; Brown, P.; Gearing, A. J. H. Design and therapeutic application of matrix metalloproteinase inhibitors Chem. Rev. 1999, 99, 2735-2776 10.1021/cr9804543
-
(1999)
Chem. Rev.
, vol.99
, pp. 2735-2776
-
-
Whittaker, M.1
Floyd, C.D.2
Brown, P.3
Gearing, A.J.H.4
-
4
-
-
84925796249
-
Beyond Iron: Non-classical Biological Functions of Bacterial Siderophores
-
Johnstone, T. C.; Nolan, E. M. Beyond Iron: Non-classical Biological Functions of Bacterial Siderophores Dalton Trans. 2015, 44, 6320-6339 10.1039/C4DT03559C
-
(2015)
Dalton Trans.
, vol.44
, pp. 6320-6339
-
-
Johnstone, T.C.1
Nolan, E.M.2
-
5
-
-
16944365890
-
Discovery of potent nonpeptide inhibitors of stromelysin using SAR by NMR
-
Hajduk, P. J.; Sheppard, G.; Nettesheim, D. G.; Olejniczak, E. T.; Shuker, S. B.; Meadows, R. P.; Steinman, D. H.; Carrera, G. M., Jr.; Marcotte, P. A.; Severin, J.; Walter, K.; Smith, H.; Gubbins, E.; Simmer, R.; Holzman, T. F.; Morgan, D. W.; Davidsen, S. K.; Summers, J. B.; Fesik, S. W. Discovery of potent nonpeptide inhibitors of stromelysin using SAR by NMR J. Am. Chem. Soc. 1997, 119, 5818-5827 10.1021/ja9702778
-
(1997)
J. Am. Chem. Soc.
, vol.119
, pp. 5818-5827
-
-
Hajduk, P.J.1
Sheppard, G.2
Nettesheim, D.G.3
Olejniczak, E.T.4
Shuker, S.B.5
Meadows, R.P.6
Steinman, D.H.7
Carrera, G.M.8
Marcotte, P.A.9
Severin, J.10
Walter, K.11
Smith, H.12
Gubbins, E.13
Simmer, R.14
Holzman, T.F.15
Morgan, D.W.16
Davidsen, S.K.17
Summers, J.B.18
Fesik, S.W.19
-
6
-
-
3142738143
-
New beginnings for matrix metalloproteinase inhibitors: Identification of high-affinity zinc-binding groups
-
Puerta, D. T.; Lewis, J. A.; Cohen, S. M. New beginnings for matrix metalloproteinase inhibitors: identification of high-affinity zinc-binding groups J. Am. Chem. Soc. 2004, 126, 8388-8389 10.1021/ja0485513
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 8388-8389
-
-
Puerta, D.T.1
Lewis, J.A.2
Cohen, S.M.3
-
7
-
-
46849089254
-
Recent developments in fragment-based drug discovery
-
Congreve, M.; Chessari, G.; Tisi, D.; Woodhead, A. J. Recent developments in fragment-based drug discovery J. Med. Chem. 2008, 51, 3661-3680 10.1021/jm8000373
-
(2008)
J. Med. Chem.
, vol.51
, pp. 3661-3680
-
-
Congreve, M.1
Chessari, G.2
Tisi, D.3
Woodhead, A.J.4
-
8
-
-
84978474564
-
Twenty Years On: The Impact of Fragments on Drug Discovery
-
Erlanson, D. A.; Fesik, S. W.; Hubbard, R. E.; Jahnke, W.; Jhoti, H. Twenty Years On: The Impact of Fragments on Drug Discovery Nat. Rev. Drug Discovery 2016, 15, 605-619 10.1038/nrd.2016.109
-
(2016)
Nat. Rev. Drug Discovery
, vol.15
, pp. 605-619
-
-
Erlanson, D.A.1
Fesik, S.W.2
Hubbard, R.E.3
Jahnke, W.4
Jhoti, H.5
-
9
-
-
26844560948
-
Potent, selective pyrone-based inhibitors of stromelysin-1
-
Puerta, D. T.; Mongan, J.; Tran, B. L.; McCammon, J. A.; Cohen, S. M. Potent, selective pyrone-based inhibitors of stromelysin-1 J. Am. Chem. Soc. 2005, 127, 14148-14149 10.1021/ja054558o
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 14148-14149
-
-
Puerta, D.T.1
Mongan, J.2
Tran, B.L.3
McCammon, J.A.4
Cohen, S.M.5
-
10
-
-
33644944087
-
A new role for old ligands: Discerning chelators for zinc metalloproteinases
-
Jacobsen, F. E.; Lewis, J. A.; Cohen, S. M. A new role for old ligands: discerning chelators for zinc metalloproteinases J. Am. Chem. Soc. 2006, 128, 3156-3157 10.1021/ja057957s
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 3156-3157
-
-
Jacobsen, F.E.1
Lewis, J.A.2
Cohen, S.M.3
-
11
-
-
77953647112
-
From Sensors to Silencers: Quinoline- and Benzimidazole-Sulfonamides as Inhibitors for Zinc Proteases
-
Rouffet, M.; de Oliveira, C. A. F.; Udi, Y.; Agrawal, A.; Sagi, I.; McCammon, J. A.; Cohen, S. M. From Sensors to Silencers: Quinoline- and Benzimidazole-Sulfonamides as Inhibitors for Zinc Proteases J. Am. Chem. Soc. 2010, 132, 8232-8233 10.1021/ja101088j
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 8232-8233
-
-
Rouffet, M.1
De Oliveira, C.A.F.2
Udi, Y.3
Agrawal, A.4
Sagi, I.5
McCammon, J.A.6
Cohen, S.M.7
-
12
-
-
0035289779
-
Experimental and Computational Approaches to Estimate Solubility and Permeability in Drug Discovery and Development Settings
-
Lipinski, C. A.; Lombardo, F.; Dominy, B. W.; Feeney, P. J. Experimental and Computational Approaches to Estimate Solubility and Permeability in Drug Discovery and Development Settings Adv. Drug Delivery Rev. 2001, 46, 3-26 10.1016/S0169-409X(00)00129-0
-
(2001)
Adv. Drug Delivery Rev.
, vol.46
, pp. 3-26
-
-
Lipinski, C.A.1
Lombardo, F.2
Dominy, B.W.3
Feeney, P.J.4
-
13
-
-
0141726877
-
A 'Rule of Three' for Fragment-based Lead Discovery
-
Congreve, M.; Carr, R.; Murray, C.; Jhoti, H. A 'Rule of Three' for Fragment-based Lead Discovery Drug Discovery Today 2003, 8, 876-877 10.1016/S1359-6446(03)02831-9
-
(2003)
Drug Discovery Today
, vol.8
, pp. 876-877
-
-
Congreve, M.1
Carr, R.2
Murray, C.3
Jhoti, H.4
-
14
-
-
0037137618
-
NMR-Based Modification of Matrix Metalloproteinase Inhibitors with Improved Bioavailability
-
Hajduk, P. J.; Shuker, S. B.; Nettesheim, D. G.; Craig, R.; Augeri, D. J.; Betebenner, D.; Albert, D. H.; Guo, Y.; Meadows, R. P.; Xu, L.; Michaelides, M.; Davidsen, S. K.; Fesik, S. W. NMR-Based Modification of Matrix Metalloproteinase Inhibitors with Improved Bioavailability J. Med. Chem. 2002, 45, 5628-5639 10.1021/jm020160g
-
(2002)
J. Med. Chem.
, vol.45
, pp. 5628-5639
-
-
Hajduk, P.J.1
Shuker, S.B.2
Nettesheim, D.G.3
Craig, R.4
Augeri, D.J.5
Betebenner, D.6
Albert, D.H.7
Guo, Y.8
Meadows, R.P.9
Xu, L.10
Michaelides, M.11
Davidsen, S.K.12
Fesik, S.W.13
-
15
-
-
0032795252
-
Transitions, Transition States, Transition State Analogues: Zinc Pyrazolylborate Chemistry Related to Zinc Enzymes
-
Vahrenkamp, H. Transitions, Transition States, Transition State Analogues: Zinc Pyrazolylborate Chemistry Related to Zinc Enzymes Acc. Chem. Res. 1999, 32, 589-596 10.1021/ar9703185
-
(1999)
Acc. Chem. Res.
, vol.32
, pp. 589-596
-
-
Vahrenkamp, H.1
-
16
-
-
0037037494
-
Elucidating Drug-Metalloprotein Interactions with Tris(pyrazolyl)borate Model Complexes
-
Puerta, D. T.; Cohen, S. M. Elucidating Drug-Metalloprotein Interactions with Tris(pyrazolyl)borate Model Complexes Inorg. Chem. 2002, 41, 5075-5082 10.1021/ic0204272
-
(2002)
Inorg. Chem.
, vol.41
, pp. 5075-5082
-
-
Puerta, D.T.1
Cohen, S.M.2
-
17
-
-
0042865983
-
From Model Complexes to Metalloprotein Inhibition: A Synergistic Approach to Structure-based Drug Discovery
-
Puerta, D. T.; Schames, J. R.; Henchman, R. H.; McCammon, J. A.; Cohen, S. M. From Model Complexes to Metalloprotein Inhibition: A Synergistic Approach to Structure-based Drug Discovery Angew. Chem., Int. Ed. 2003, 42, 3772-3774 10.1002/anie.200351433
-
(2003)
Angew. Chem., Int. Ed.
, vol.42
, pp. 3772-3774
-
-
Puerta, D.T.1
Schames, J.R.2
Henchman, R.H.3
McCammon, J.A.4
Cohen, S.M.5
-
19
-
-
75749098088
-
Chelator fragment libraries for targeting metalloproteinases
-
Agrawal, A.; Johnson, S. L.; Jacobsen, J. A.; Miller, M. T.; Chen, L.-H.; Pellecchia, M.; Cohen, S. M. Chelator fragment libraries for targeting metalloproteinases ChemMedChem 2010, 5, 195-199 10.1002/cmdc.200900516
-
(2010)
ChemMedChem
, vol.5
, pp. 195-199
-
-
Agrawal, A.1
Johnson, S.L.2
Jacobsen, J.A.3
Miller, M.T.4
Chen, L.-H.5
Pellecchia, M.6
Cohen, S.M.7
-
20
-
-
78751661570
-
Identifying Chelators for Metalloprotein Inhibitors Using a Fragment-Based Approach
-
Jacobsen, J. A.; Fullagar, J. L.; Miller, M. T.; Cohen, S. M. Identifying Chelators for Metalloprotein Inhibitors Using a Fragment-Based Approach J. Med. Chem. 2011, 54, 591-602 10.1021/jm101266s
-
(2011)
J. Med. Chem.
, vol.54
, pp. 591-602
-
-
Jacobsen, J.A.1
Fullagar, J.L.2
Miller, M.T.3
Cohen, S.M.4
-
21
-
-
84875444608
-
Antagonism of a Zinc Metalloprotease Using a Unique Metal-Chelating Scaffold: Tropolones as Inhibitors of P. aeruginosa Elastase
-
Fullagar, J. L.; Garner, A. L.; Struss, A. K.; Day, J. A.; Martin, D. P.; Yu, J.; Cai, X. Q.; Janda, K. D.; Cohen, S. M. Antagonism of a Zinc Metalloprotease Using a Unique Metal-Chelating Scaffold: Tropolones as Inhibitors of P. aeruginosa Elastase Chem. Commun. 2013, 49, 3197-3199 10.1039/c3cc41191e
-
(2013)
Chem. Commun.
, vol.49
, pp. 3197-3199
-
-
Fullagar, J.L.1
Garner, A.L.2
Struss, A.K.3
Day, J.A.4
Martin, D.P.5
Yu, J.6
Cai, X.Q.7
Janda, K.D.8
Cohen, S.M.9
-
22
-
-
85013833905
-
Discovery of an Inhibitor of the Proteasome Subunit Rpn11
-
Perez, C.; Li, J.; Parlati, F.; Rouffet, M.; Ma, Y.; Mackinnon, A. L.; Chou, T.-F.; Deshaies, R. J.; Cohen, S. M. Discovery of an Inhibitor of the Proteasome Subunit Rpn11 J. Med. Chem. 2017, 60, 1343-1361 10.1021/acs.jmedchem.6b01379
-
(2017)
J. Med. Chem.
, vol.60
, pp. 1343-1361
-
-
Perez, C.1
Li, J.2
Parlati, F.3
Rouffet, M.4
Ma, Y.5
Mackinnon, A.L.6
Chou, T.-F.7
Deshaies, R.J.8
Cohen, S.M.9
-
23
-
-
79956366646
-
Proteasome Inhibitors in Cancer Therapy
-
Crawford, L. J.; Walker, B.; Irvine, A. E. Proteasome Inhibitors in Cancer Therapy J. Cell Commun. Signal 2011, 5, 101-110 10.1007/s12079-011-0121-7
-
(2011)
J. Cell Commun. Signal
, vol.5
, pp. 101-110
-
-
Crawford, L.J.1
Walker, B.2
Irvine, A.E.3
-
24
-
-
78049264771
-
The 26S proteasome: Assembly and Function of a Destructive Machine
-
Gallastegui, N.; Groll, M. The 26S proteasome: Assembly and Function of a Destructive Machine Trends Biochem. Sci. 2010, 35, 634-642 10.1016/j.tibs.2010.05.005
-
(2010)
Trends Biochem. Sci.
, vol.35
, pp. 634-642
-
-
Gallastegui, N.1
Groll, M.2
-
25
-
-
19344364762
-
JAMM: A Metalloprotease-like Zinc Site in the Proteasome and Signalosome
-
Ambroggio, X. I.; Rees, D. C.; Deshaies, R. J. JAMM: A Metalloprotease-like Zinc Site in the Proteasome and Signalosome PLoS Biol. 2003, 2, e2 10.1371/journal.pbio.0020002
-
(2003)
PLoS Biol.
, vol.2
, pp. e2
-
-
Ambroggio, X.I.1
Rees, D.C.2
Deshaies, R.J.3
-
26
-
-
0037131243
-
Role of Rpn11 Metalloprotease in Deubiquitination and Degradation by the 26S Proteasome
-
Verma, R.; Aravind, L.; Oania, R.; McDonald, W. H.; Yates, J. R.; Koonin, E. V.; Deshaies, R. J. Role of Rpn11 Metalloprotease in Deubiquitination and Degradation by the 26S Proteasome Science 2002, 298, 611-615 10.1126/science.1075898
-
(2002)
Science
, vol.298
, pp. 611-615
-
-
Verma, R.1
Aravind, L.2
Oania, R.3
McDonald, W.H.4
Yates, J.R.5
Koonin, E.V.6
Deshaies, R.J.7
-
27
-
-
85013819302
-
Capzimin is a Potent and Specific Inhibitor of Proteasome Isopeptidase Rpn11
-
Li, J.; Yakushi, T.; Parlati, F.; Mackinnon, A. L.; Perez, C.; Ma, Y.; Carter, K. P.; Colayco, S.; Magnuson, G.; Brown, B.; Nguyen, K.; Vasile, S.; Suyama, E.; Smith, L. H.; Sergienko, E.; Pinkerton, A. B.; Chung, T. D. Y.; Palmer, A. E.; Pass, I.; Hess, S.; Cohen, S. M.; Deshaies, R. J. Capzimin is a Potent and Specific Inhibitor of Proteasome Isopeptidase Rpn11 Nat. Chem. Biol. 2017, 13, 486-493 10.1038/nchembio.2326
-
(2017)
Nat. Chem. Biol.
, vol.13
, pp. 486-493
-
-
Li, J.1
Yakushi, T.2
Parlati, F.3
Mackinnon, A.L.4
Perez, C.5
Ma, Y.6
Carter, K.P.7
Colayco, S.8
Magnuson, G.9
Brown, B.10
Nguyen, K.11
Vasile, S.12
Suyama, E.13
Smith, L.H.14
Sergienko, E.15
Pinkerton, A.B.16
Chung, T.D.Y.17
Palmer, A.E.18
Pass, I.19
Hess, S.20
Cohen, S.M.21
Deshaies, R.J.22
more..
-
28
-
-
84886506966
-
Investigating the Selectivity of Metalloenzyme Inhibitors
-
Day, J. A.; Cohen, S. M. Investigating the Selectivity of Metalloenzyme Inhibitors J. Med. Chem. 2013, 56, 7997-8007 10.1021/jm401053m
-
(2013)
J. Med. Chem.
, vol.56
, pp. 7997-8007
-
-
Day, J.A.1
Cohen, S.M.2
-
29
-
-
84942516466
-
Investigating the Selectivity of Metalloenzyme Inhibitors in the Presence of Competing Metalloproteins
-
Chen, Y.; Cohen, S. M. Investigating the Selectivity of Metalloenzyme Inhibitors in the Presence of Competing Metalloproteins ChemMedChem 2015, 10, 1733-1738 10.1002/cmdc.201500293
-
(2015)
ChemMedChem
, vol.10
, pp. 1733-1738
-
-
Chen, Y.1
Cohen, S.M.2
-
30
-
-
85027440810
-
The Effect of Metalloprotein Inhibitors on Cellular Metal Ion Content and Distribution
-
Chen, Y.; Lai, B.; Zhang, Z.; Cohen, S. M. The Effect of Metalloprotein Inhibitors on Cellular Metal Ion Content and Distribution Metallomics 2017, 9, 250-257 10.1039/C6MT00267F
-
(2017)
Metallomics
, vol.9
, pp. 250-257
-
-
Chen, Y.1
Lai, B.2
Zhang, Z.3
Cohen, S.M.4
-
31
-
-
84887128203
-
Metalloprotein-Inhibitor Binding: Human Carbonic Anhydrase II as a Model for Probing Metal-Ligand Interactions in a Metalloprotein Active Site
-
Martin, D. P.; Hann, Z. S.; Cohen, S. M. Metalloprotein-Inhibitor Binding: Human Carbonic Anhydrase II as a Model for Probing Metal-Ligand Interactions in a Metalloprotein Active Site Inorg. Chem. 2013, 52, 12207-12215 10.1021/ic400295f
-
(2013)
Inorg. Chem.
, vol.52
, pp. 12207-12215
-
-
Martin, D.P.1
Hann, Z.S.2
Cohen, S.M.3
-
32
-
-
85017097386
-
Effect of donor atom identity on metal-binding pharmacophore coordination
-
Dick, B. L.; Patel, A.; McCammon, J. A.; Cohen, S. M. Effect of donor atom identity on metal-binding pharmacophore coordination JBIC, J. Biol. Inorg. Chem. 2017, 22, 605-613 10.1007/s00775-017-1454-3
-
(2017)
JBIC, J. Biol. Inorg. Chem.
, vol.22
, pp. 605-613
-
-
Dick, B.L.1
Patel, A.2
McCammon, J.A.3
Cohen, S.M.4
-
33
-
-
84906874907
-
Exploring the Influence of the Protein Environment on Metal-Binding Pharmacophores
-
Martin, D. P.; Blachly, P. G.; McCammon, J. A.; Cohen, S. M. Exploring the Influence of the Protein Environment on Metal-Binding Pharmacophores J. Med. Chem. 2014, 57, 7126-7135 10.1021/jm500984b
-
(2014)
J. Med. Chem.
, vol.57
, pp. 7126-7135
-
-
Martin, D.P.1
Blachly, P.G.2
McCammon, J.A.3
Cohen, S.M.4
-
34
-
-
84897998448
-
Unconventional' Coordination Chemistry by Metal Chelating Fragments in a Metalloprotein Active Site
-
Martin, D. P.; Blachly, P. G.; Marts, A. R.; Woodruff, T. M.; deOliveira, C. A. F.; McCammon, J. A.; Tierney, D. L.; Cohen, S. M. Unconventional' Coordination Chemistry by Metal Chelating Fragments in a Metalloprotein Active Site J. Am. Chem. Soc. 2014, 136, 5400-5406 10.1021/ja500616m
-
(2014)
J. Am. Chem. Soc.
, vol.136
, pp. 5400-5406
-
-
Martin, D.P.1
Blachly, P.G.2
Marts, A.R.3
Woodruff, T.M.4
DeOliveira, C.A.F.5
McCammon, J.A.6
Tierney, D.L.7
Cohen, S.M.8
-
35
-
-
84885181482
-
Crystallographic fragment screening and structure-based optimization yields a new class of influenza endonuclease inhibitors
-
Bauman, J. D.; Patel, D.; Baker, S. F.; Vijayan, R. S.; Xiang, A.; Parhi, A. K.; Martinez-Sobrido, L.; LaVoie, E. J.; Das, K.; Arnold, E. Crystallographic fragment screening and structure-based optimization yields a new class of influenza endonuclease inhibitors ACS Chem. Biol. 2013, 8, 2501-2508 10.1021/cb400400j
-
(2013)
ACS Chem. Biol.
, vol.8
, pp. 2501-2508
-
-
Bauman, J.D.1
Patel, D.2
Baker, S.F.3
Vijayan, R.S.4
Xiang, A.5
Parhi, A.K.6
Martinez-Sobrido, L.7
LaVoie, E.J.8
Das, K.9
Arnold, E.10
-
36
-
-
0038792294
-
Discovery and structural modification of inhibitors of methionine aminopeptidases from Escherichia coli and Saccharomyces cerevisiae
-
Luo, Q. L.; Li, J. Y.; Liu, Z. Y.; Chen, L. L.; Li, J.; Qian, Z.; Shen, Q.; Li, Y.; Lushington, G. H.; Ye, Q. Z.; Nan, F. J. Discovery and structural modification of inhibitors of methionine aminopeptidases from Escherichia coli and Saccharomyces cerevisiae J. Med. Chem. 2003, 46, 2631-2640 10.1021/jm0300532
-
(2003)
J. Med. Chem.
, vol.46
, pp. 2631-2640
-
-
Luo, Q.L.1
Li, J.Y.2
Liu, Z.Y.3
Chen, L.L.4
Li, J.5
Qian, Z.6
Shen, Q.7
Li, Y.8
Lushington, G.H.9
Ye, Q.Z.10
Nan, F.J.11
-
37
-
-
84877701677
-
3-Hydroxypyridin-2-thione as novel zinc binding group for selective histone deacetylase inhibition
-
Patil, V.; Sodji, Q. H.; Kornacki, J. R.; Mrksich, M.; Oyelere, A. K. 3-Hydroxypyridin-2-thione as novel zinc binding group for selective histone deacetylase inhibition J. Med. Chem. 2013, 56, 3492-3506 10.1021/jm301769u
-
(2013)
J. Med. Chem.
, vol.56
, pp. 3492-3506
-
-
Patil, V.1
Sodji, Q.H.2
Kornacki, J.R.3
Mrksich, M.4
Oyelere, A.K.5
-
38
-
-
84870237988
-
Design and evaluation of azaindole-substituted N-hydroxypyridones as glyoxalase i inhibitors
-
Chiba, T.; Ohwada, J.; Sakamoto, H.; Kobayashi, T.; Fukami, T. A.; Irie, M.; Miura, T.; Ohara, K.; Koyano, H. Design and evaluation of azaindole-substituted N-hydroxypyridones as glyoxalase I inhibitors Bioorg. Med. Chem. Lett. 2012, 22, 7486-7489 10.1016/j.bmcl.2012.10.045
-
(2012)
Bioorg. Med. Chem. Lett.
, vol.22
, pp. 7486-7489
-
-
Chiba, T.1
Ohwada, J.2
Sakamoto, H.3
Kobayashi, T.4
Fukami, T.A.5
Irie, M.6
Miura, T.7
Ohara, K.8
Koyano, H.9
|