-
1
-
-
0036882393
-
Human and parasitic papainlike cysteine proteases: Their role in physiology and pathology and recent developments in inhibitor design
-
Lecaille, F.; Kaleta, J.; Bromme, D. Human and parasitic papainlike cysteine proteases: their role in physiology and pathology and recent developments in inhibitor design. Chem. Rev., 2002, 102, 4459-4488.
-
(2002)
Chem. Rev.
, vol.102
, pp. 4459-4488
-
-
Lecaille, F.1
Kaleta, J.2
Bromme, D.3
-
2
-
-
0036882396
-
Irreversible inhibitors of serine, cysteine, and threonine proteases
-
Powers, J.C.; Asgian, J.L.; Ekici, O.D.; James, K.E. Irreversible inhibitors of serine, cysteine, and threonine proteases. Chem. Rev., 2002, 102, 4639-4750.
-
(2002)
Chem. Rev.
, vol.102
, pp. 4639-4750
-
-
Powers, J.C.1
Asgian, J.L.2
Ekici, O.D.3
James, K.E.4
-
3
-
-
0034930561
-
Evolutionary lines of cysteine peptidases
-
Barrett, A.J.; Rawlings, N.D. Evolutionary lines of cysteine peptidases. Biol. Chem., 2001, 382, 727-733.
-
(2001)
Biol. Chem.
, vol.382
, pp. 727-733
-
-
Barrett, A.J.1
Rawlings, N.D.2
-
4
-
-
33646058296
-
Thiol proteases: Inhibitors and potential therapeutic targets
-
Leung-Toung, R.; Zhao, Y.; Li, W.; Tam, T.F.; Karimian, K.; Spino, M. Thiol proteases: inhibitors and potential therapeutic targets. Curr. Med. Chem., 2006, 13, 547-581.
-
(2006)
Curr. Med. Chem.
, vol.13
, pp. 547-581
-
-
Leung-Toung, R.1
Zhao, Y.2
Li, W.3
Tam, T.F.4
Karimian, K.5
Spino, M.6
-
5
-
-
0036882392
-
Viral proteases
-
Tong, L. Viral proteases. Chem. Rev., 2002, 102, 4609-4626.
-
(2002)
Chem. Rev.
, vol.102
, pp. 4609-4626
-
-
Tong, L.1
-
6
-
-
0037561920
-
Characterization of a novel coronavirus associated with severe acute respiratory syndrome
-
DOI 10.1126/science.1085952
-
Rota, P.A.; Oberste, M.S.; Monroe, S.S.; Nix, W.A.; Campagnoli, R.; Icenogle, J.P.; Penaranda, S.; Bankamp, B.; Maher, K.; Chen, M.H.; Tong, S.; Tamin, A.; Lowe, L.; Frace, M.; DeRisi, J.L.; Chen, Q.; Wang, D.; Erdman, D.D.; Peret, T.C.; Burns, C.; Ksiazek, T.G.; Rollin, P.E.; Sanchez, A.; Liffick, S.; Holloway, B.; Limor, J.; McCaustland, K.; Olsen-Rasmussen, M.; Fouchier, R.; Gunther, S.; Osterhaus, A.D.; Drosten, C.; Pallansch, M.A.; Anderson, L.J.; Bellini, W.J. Characterization of a novel coronavirus associated with severe acute respiratory syndrome. Science, 2003, 300, 1394-1399. (Pubitemid 36638152)
-
(2003)
Science
, vol.300
, Issue.5624
, pp. 1394-1399
-
-
Rota, P.A.1
Oberste, M.S.2
Monroe, S.S.3
Nix, W.A.4
Campagnoli, R.5
Icenogle, J.P.6
Penaranda, S.7
Bankamp, B.8
Maher, K.9
Chen, M.-H.10
Tong, S.11
Tamin, A.12
Lowe, L.13
Frace, M.14
Derisi, J.L.15
Chen, Q.16
Wang, D.17
Erdman, D.D.18
Peret, T.C.T.19
Burns, C.20
Ksiazek, T.G.21
Rollin, P.E.22
Sanchez, A.23
Liffick, S.24
Holloway, B.25
Limor, J.26
McCaustland, K.27
Olsen-Rasmussen, M.28
Fouchier, R.29
Gunther, S.30
Osterhaus, A.D.H.E.31
Drosten, C.32
Pallansch, M.A.33
Anderson, L.J.34
Bellini, W.J.35
more..
-
7
-
-
0038120984
-
pro) Structure: Basis for design of anti-SARS drugs
-
DOI 10.1126/science.1085658
-
Anand, K.; Ziebuhr, J.; Wadhwani, P.; Mesters, J.R.; Hilgenfeld, R. Coronavirus main proteinase (3CLpro) structure: basis for design of anti-SARS drugs. Science (Washington, DC, U. S.), 2003, 300,1763-1767. (Pubitemid 36712575)
-
(2003)
Science
, vol.300
, Issue.5626
, pp. 1763-1767
-
-
Anand, K.1
Ziebuhr, J.2
Wadhwani, P.3
Mesters, J.R.4
Hilgenfeld, R.5
-
8
-
-
10744228371
-
Structure-based design, synthesis, and biological evaluation of irreversible human rhinovirus 3C protease inhibitors. 8. Pharmacological optimization of orally bioavailable 2-pyridone-containing peptidomimetics
-
Dragovich, P.S.; Prins, T.J.; Zhou, R.; Johnson, T.O.; Hua, Y.; Luu, H.T.; Sakata, S.K.; Brown, E.L.; Maldonado, F.C.; Tuntland, T.; Lee, C.A.; Fuhrman, S.A.; Zalman, L.S.; Patick, A.K.; Matthews, D.A.; Wu, E.Y.; Guo, M.; Borer, B.C.; Nayyar, N.K.; Moran, T.; Chen, L.; Rejto, P.A.; Rose, P.W.; Guzman, M.C.; Dovalsantos, E.Z.; Lee, S.; McGee, K.; Mohajeri, M.; Liese, A.; Tao, J.; Kosa, M.B.; Liu, B.; Batugo, M.R.; Gleeson, J.P.; Wu, Z.P.; Liu, J.; Meador, J.W., 3rd; Ferre, R.A. Structure-based design, synthesis, and biological evaluation of irreversible human rhinovirus 3C protease inhibitors. 8. Pharmacological optimization of orally bioavailable 2-pyridone-containing peptidomimetics. J. Med. Chem., 2003, 46, 4572-4585.
-
(2003)
J. Med. Chem.
, vol.46
, pp. 4572-4585
-
-
Dragovich, P.S.1
Prins, T.J.2
Zhou, R.3
Johnson, T.O.4
Hua, Y.5
Luu, H.T.6
Sakata, S.K.7
Brown, E.L.8
Maldonado, F.C.9
Tuntland, T.10
Lee, C.A.11
Fuhrman, S.A.12
Zalman, L.S.13
Patick, A.K.14
Matthews, D.A.15
Wu, E.Y.16
Guo, M.17
Borer, B.C.18
Nayyar, N.K.19
Moran, T.20
Chen, L.21
Rejto, P.A.22
Rose, P.W.23
Guzman, M.C.24
Dovalsantos, E.Z.25
Lee, S.26
McGee, K.27
Mohajeri, M.28
Liese, A.29
Tao, J.30
Kosa, M.B.31
Liu, B.32
Batugo, M.R.33
Gleeson, J.P.34
Wu, Z.P.35
Liu, J.36
Meador III, J.W.37
Ferre, R.A.38
more..
-
9
-
-
6444244485
-
Crystal structures of reversible ketone-Based inhibitors of the cysteine protease cruzain
-
Huang, L.; Brinen, L.S.; Ellman, J.A. Crystal structures of reversible ketone-Based inhibitors of the cysteine protease cruzain. Bioorg. Med. Chem., 2003, 11, 21-29.
-
(2003)
Bioorg. Med. Chem.
, vol.11
, pp. 21-29
-
-
Huang, L.1
Brinen, L.S.2
Ellman, J.A.3
-
10
-
-
0035282807
-
Cyclic ketone inhibitors of the cysteine protease cathepsin K
-
DOI 10.1021/jm000320t
-
Marquis, R.W.; Ru, Y.; Zeng, J.; Trout, R.E.; LoCastro, S.M.; Gribble, A.D.; Witherington, J.; Fenwick, A.E.; Garnier, B.; Tomaszek, T.; Tew, D.; Hemling, M.E.; Quinn, C.J.; Smith, W.W.; Zhao, B.; McQueney, M.S.; Janson, C.A.; D'Alessio, K.; Veber, D.F. Cyclic ketone inhibitors of the cysteine protease cathepsin K. J. Med. Chem., 2001, 44, 725-736. (Pubitemid 32171669)
-
(2001)
Journal of Medicinal Chemistry
, vol.44
, Issue.5
, pp. 725-736
-
-
Marquis, R.W.1
Ru, Y.2
Zeng, J.3
Lee Trout, R.E.4
Locastro, S.M.5
Gribble, A.D.6
Witherington, J.7
Fenwick, A.E.8
Garnier, B.9
Tomaszek, T.10
Tew, D.11
Hemling, M.E.12
Quinn, C.J.13
Smith, W.W.14
Zhao, B.15
McQueney, M.S.16
Janson, C.A.17
D'Alessio, K.18
Veber, D.F.19
-
11
-
-
0037447948
-
Structure-based approach to falcipain-2 inhibitors: Synthesis and biological evaluation of 1,6,7-Trisubstituted dihydroisoquinolines and isoquinolines
-
Batra, S.; Sabnis, Y.A.; Rosenthal, P.J.; Avery, M.A. Structure-based approach to falcipain-2 inhibitors: synthesis and biological evaluation of 1,6,7-Trisubstituted dihydroisoquinolines and isoquinolines. Bioorg. Med. Chem., 2003, 11, 2293-2299.
-
(2003)
Bioorg. Med. Chem.
, vol.11
, pp. 2293-2299
-
-
Batra, S.1
Sabnis, Y.A.2
Rosenthal, P.J.3
Avery, M.A.4
-
12
-
-
0036244780
-
Homology modeling of falcipain-2: Validation, de novo ligand design and synthesis of novel inhibitors
-
Sabnis, Y.; Rosenthal, P.J.; Desai, P.; Avery, M.A. Homology modeling of falcipain-2: validation, de novo ligand design and synthesis of novel inhibitors. J. Biomol. Struct. Dyn., 2002, 19, 765-774.
-
(2002)
J. Biomol. Struct. Dyn.
, vol.19
, pp. 765-774
-
-
Sabnis, Y.1
Rosenthal, P.J.2
Desai, P.3
Avery, M.A.4
-
13
-
-
14444272282
-
Structure-based design, synthesis, and biological evaluation of irreversible human rhinovirus 3C protease inhibitors. 1. Michael acceptor structure-activity studies
-
Dragovich, P.S.; Webber, S.E.; Babine, R.E.; Fuhrman, S.A.; Patick, A.K.; Matthews, D.A.; Lee, C.A.; Reich, S.H.; Prins, T.J.; Marakovits, J.T.; Littlefield, E.S.; Zhou, R.; Tikhe, J.; Ford, C.E.; Wallace, M.B.; Meador, J.W., 3rd; Ferre, R.A.; Brown, E.L.; Binford, S.L.; Harr, J.E.; DeLisle, D.M.; Worland, S.T. Structure-based design, synthesis, and biological evaluation of irreversible human rhinovirus 3C protease inhibitors. 1. Michael acceptor structure-activity studies. J. Med. Chem., 1998, 41, 2806-2818.
-
(1998)
J. Med. Chem.
, vol.41
, pp. 2806-2818
-
-
Dragovich, P.S.1
Webber, S.E.2
Babine, R.E.3
Fuhrman, S.A.4
Patick, A.K.5
Matthews, D.A.6
Lee, C.A.7
Reich, S.H.8
Prins, T.J.9
Marakovits, J.T.10
Littlefield, E.S.11
Zhou, R.12
Tikhe, J.13
Ford, C.E.14
Wallace, M.B.15
Meador III, J.W.16
Ferre, R.A.17
Brown, E.L.18
Binford, S.L.19
Harr, J.E.20
DeLisle, D.M.21
Worland, S.T.22
more..
-
14
-
-
39749155747
-
Development of peptidomimetics with a vinyl sulfone warhead as irreversible falcipain-2 inhibitors
-
Ettari, R.; Nizi, E.; Di Francesco, M.E.; Dude, M.A.; Pradel, G.; Vicik, R.; Schirmeister, T.; Micale, N.; Grasso, S.; Zappala, M. Development of peptidomimetics with a vinyl sulfone warhead as irreversible falcipain-2 inhibitors. J. Med. Chem., 2008, 51, 988-996.
-
(2008)
J. Med. Chem.
, vol.51
, pp. 988-996
-
-
Ettari, R.1
Nizi, E.2
Di Francesco, M.E.3
Dude, M.A.4
Pradel, G.5
Vicik, R.6
Schirmeister, T.7
Micale, N.8
Grasso, S.9
Zappala, M.10
-
15
-
-
0033765620
-
A survey of calpain inhibitors
-
Donkor, I.O. A survey of calpain inhibitors. Curr. Med. Chem., 2000, 7, 1171-1188.
-
(2000)
Curr. Med. Chem.
, vol.7
, pp. 1171-1188
-
-
Donkor, I.O.1
-
16
-
-
0036682237
-
Synthesis and in vitro studies of novel pyrimidinyl peptidomimetics as potential antimalarial therapeutic agents
-
Zhu, S.; Hudson, T.H.; Kyle, D.E.; Lin, A.J. Synthesis and in vitro studies of novel pyrimidinyl peptidomimetics as potential antimalarial therapeutic agents. J. Med. Chem., 2002, 45, 3491-3496.
-
(2002)
J. Med. Chem.
, vol.45
, pp. 3491-3496
-
-
Zhu, S.1
Hudson, T.H.2
Kyle, D.E.3
Lin, A.J.4
-
17
-
-
33751577809
-
Discovering severe acute respiratory syndrome coronavirus 3CL protease inhibitors: Virtual screening, surface plasmon resonance, and fluorescence resonance energy transfer assays
-
Chen, L.; Chen, S.; Gui, C.; Shen, J.; Shen, X.; Jiang, H. Discovering severe acute respiratory syndrome coronavirus 3CL protease inhibitors: virtual screening, surface plasmon resonance, and fluorescence resonance energy transfer assays. J. Biomol. Screen., 2006, 11, 915-921.
-
(2006)
J. Biomol. Screen.
, vol.11
, pp. 915-921
-
-
Chen, L.1
Chen, S.2
Gui, C.3
Shen, J.4
Shen, X.5
Jiang, H.6
-
18
-
-
41649107991
-
Structure-based virtual screening against SARS-3CL(pro) to identify novel non-peptidic hits
-
Mukherjee, P.; Desai, P.; Ross, L.; White, E.L.; Avery, M.A. Structure-based virtual screening against SARS-3CL(pro) to identify novel non-peptidic hits. Bioorg. Med. Chem., 2008, 16,4138-4149.
-
(2008)
Bioorg. Med. Chem.
, vol.16
, pp. 4138-4149
-
-
Mukherjee, P.1
Desai, P.2
Ross, L.3
White, E.L.4
Avery, M.A.5
-
19
-
-
57649122948
-
-
[Access date: August 8, 2009].
-
World Malaria Report 2008, http://malaria.who.int/wmr2008/ [Access date: August 8, 2009].
-
World Malaria Report 2008
-
-
-
21
-
-
0035997361
-
Biological roles of proteases in parasitic protozoa
-
Klemba, M.; Goldberg, D.E. Biological roles of proteases in parasitic protozoa. Annu. Rev. Biochem., 2002, 71, 275-305.
-
(2002)
Annu. Rev. Biochem.
, vol.71
, pp. 275-305
-
-
Klemba, M.1
Goldberg, D.E.2
-
22
-
-
0036183460
-
Hydrolysis of erythrocyte proteins by proteases of malaria parasites
-
Rosenthal, P.J. Hydrolysis of erythrocyte proteins by proteases of malaria parasites. Curr. Opin. Hematol., 2002, 9, 140-145.
-
(2002)
Curr. Opin. Hematol.
, vol.9
, pp. 140-145
-
-
Rosenthal, P.J.1
-
23
-
-
1442326738
-
Structure-based approaches to the development of novel anti-malarials
-
DOI 10.2174/1389450043490587
-
Brady, R.L.; Cameron, A. Structure-based approaches to the development of novel anti-malarials. Curr. Drug Targets, 2004, 5,137-149. (Pubitemid 38279412)
-
(2004)
Current Drug Targets
, vol.5
, Issue.2
, pp. 137-149
-
-
Brady, R.L.1
Cameron, A.2
-
25
-
-
0034666133
-
Characterization of native and recombinant falcipain-2, a principal trophozoite cysteine protease and essential hemoglobinase of Plasmodium falciparum
-
Shenai, B.R.; Sijwali, P.S.; Singh, A.; Rosenthal, P.J. Characterization of native and recombinant falcipain-2, a principal trophozoite cysteine protease and essential hemoglobinase of Plasmodium falciparum. J. Biol. Chem., 2000, 275, 29000-29010.
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 29000-29010
-
-
Shenai, B.R.1
Sijwali, P.S.2
Singh, A.3
Rosenthal, P.J.4
-
26
-
-
12344273618
-
Biosynthesis, localization, and processing of falcipain cysteine proteases of Plasmodium falciparum
-
DOI 10.1016/j.molbiopara.2004.11.009, PII S0166685104003135
-
Dahl, E.L.; Rosenthal, P.J. Biosynthesis, localization, and processing of falcipain cysteine proteases of Plasmodium falciparum. Mol. Biochem. Parasitol., 2005, 139, 205-212. (Pubitemid 40128216)
-
(2005)
Molecular and Biochemical Parasitology
, vol.139
, Issue.2
, pp. 205-212
-
-
Dahl, E.L.1
Rosenthal, P.J.2
-
27
-
-
0035644195
-
Expression and characterization of the Plasmodium falciparum haemoglobinase falcipain-3
-
DOI 10.1042/0264-6021:3600481
-
Sijwali, P.S.; Shenai, B.R.; Gut, J.; Singh, A.; Rosenthal, P.J. Expression and characterization of the Plasmodium falciparum haemoglobinase falcipain-3. Biochem. J., 2001, 360, 481-489. (Pubitemid 33151343)
-
(2001)
Biochemical Journal
, vol.360
, Issue.2
, pp. 481-489
-
-
Sijwali, P.S.1
Shenai, B.R.2
Gut, J.3
Singh, A.4
Rosenthal, P.J.5
-
28
-
-
33748328016
-
Gene disruptions demonstrate independent roles for the four falcipain cysteine proteases of Plasmodium falciparum
-
Sijwali, P.S.; Koo, J.; Singh, N.; Rosenthal, P.J. Gene disruptions demonstrate independent roles for the four falcipain cysteine proteases of Plasmodium falciparum. Mol. Biochem. Parasitol., 2006, 150, 96-106.
-
(2006)
Mol. Biochem. Parasitol.
, vol.150
, pp. 96-106
-
-
Sijwali, P.S.1
Koo, J.2
Singh, N.3
Rosenthal, P.J.4
-
29
-
-
0035986688
-
Cysteine protease of malaria parasites: Targets for chemotherapy
-
DOI 10.2174/1381612023394197
-
Rosenthal, P.J.; Sijwali, P.S.; Singh, A.; Shenai, B.R. Cysteine proteases of malaria parasites: targets for chemotherapy. Curr. Pharm. Des., 2002, 8, 1659-1672. (Pubitemid 34752832)
-
(2002)
Current Pharmaceutical Design
, vol.8
, Issue.18
, pp. 1659-1672
-
-
Rosenthal, P.J.1
Sijwali, P.S.2
Singh, A.3
Shenai, B.R.4
-
30
-
-
2242432614
-
A role for the protease falcipain 1 in host cell invasion by the human malaria parasite
-
DOI 10.1126/science.1077426
-
Greenbaum, D.C.; Baruch, A.; Grainger, M.; Bozdech, Z.; Medzihradszky, K.F.; Engel, J.; DeRisi, J.; Holder, A.A.; Bogyo, M. A role for the protease falcipain 1 in host cell invasion by the human malaria parasite. Science, 2002, 298, 2002-2006. (Pubitemid 35425258)
-
(2002)
Science
, vol.298
, Issue.5600
, pp. 2002-2006
-
-
Greenbaum, D.C.1
Baruch, A.2
Grainger, M.3
Bozdech, Z.4
Medzihradszky, K.F.5
Engel, J.6
Derisi, J.7
Holder, A.A.8
Bogyo, M.9
-
31
-
-
1842533231
-
Gene disruption confirms a critical role for the cysteine protease falcipain-2 in hemoglobin hydrolysis by Plasmodium falciparum
-
Sijwali, P.S.; Rosenthal, P.J. Gene disruption confirms a critical role for the cysteine protease falcipain-2 in hemoglobin hydrolysis by Plasmodium falciparum. Proc. Natl. Acad. Sci. USA, 2004, 101, 4384-4389.
-
(2004)
Proc. Natl. Acad. Sci. USA
, vol.101
, pp. 4384-4389
-
-
Sijwali, P.S.1
Rosenthal, P.J.2
-
32
-
-
0036682503
-
Plasmodium falciparum cysteine protease falcipain-2 cleaves erythrocyte membrane skeletal proteins at late stages of parasite development
-
Hanspal, M.; Dua, M.; Takakuwa, Y.; Chishti, A.H.; Mizuno, A. Plasmodium falciparum cysteine protease falcipain-2 cleaves erythrocyte membrane skeletal proteins at late stages of parasite development. Blood, 2002, 100, 1048-1054.
-
(2002)
Blood
, vol.100
, pp. 1048-1054
-
-
Hanspal, M.1
Dua, M.2
Takakuwa, Y.3
Chishti, A.H.4
Mizuno, A.5
-
33
-
-
0037370645
-
Probing the structure of falcipain-3, a cysteine protease from Plasmodium falciparum: Comparative protein modeling and docking studies
-
Sabnis, Y.A.; Desai, P.V.; Rosenthal, P.J.; Avery, M.A. Probing the structure of falcipain-3, a cysteine protease from Plasmodium falciparum: Comparative protein modeling and docking studies. Protein Sci., 2003, 12, 501-509.
-
(2003)
Protein Sci.
, vol.12
, pp. 501-509
-
-
Sabnis, Y.A.1
Desai, P.V.2
Rosenthal, P.J.3
Avery, M.A.4
-
34
-
-
0035163181
-
The impact of whole genome sequence data on drug discovery - A malaria case study
-
Joachimiak, M.P.; Chang, C.; Rosenthal, P.J.; Cohen, F.E. The impact of whole genome sequence data on drug discovery - a malaria case study. Mol. Med., 2001, 7, 698-710.
-
(2001)
Mol. Med.
, vol.7
, pp. 698-710
-
-
Joachimiak, M.P.1
Chang, C.2
Rosenthal, P.J.3
Cohen, F.E.4
-
35
-
-
4544367028
-
Homology modeling and mutagenesis analyses of Plasmodium falciparum falcipain 2A: Implications for rational drug design
-
Goh, L.L.; Sim, T.S. Homology modeling and mutagenesis analyses of Plasmodium falciparum falcipain 2A: implications for rational drug design. Biochem. Biophys. Res. Commun., 2004, 323,565-572.
-
(2004)
Biochem. Biophys. Res. Commun.
, vol.323
, pp. 565-572
-
-
Goh, L.L.1
Sim, T.S.2
-
36
-
-
33748746156
-
Structural and functional characterization of Falcipain-2, a hemoglobinase from the malarial parasite Plasmodium falciparum
-
Hogg, T.; Nagarajan, K.; Herzberg, S.; Chen, L.; Shen, X.; Jiang, H.; Wecke, M.; Blohmke, C.; Hilgenfeld, R.; Schmidt, C.L. Structural and functional characterization of Falcipain-2, a hemoglobinase from the malarial parasite Plasmodium falciparum. J. Biol. Chem., 2006, 281, 25425-25437.
-
(2006)
J. Biol. Chem.
, vol.281
, pp. 25425-25437
-
-
Hogg, T.1
Nagarajan, K.2
Herzberg, S.3
Chen, L.4
Shen, X.5
Jiang, H.6
Wecke, M.7
Blohmke, C.8
Hilgenfeld, R.9
Schmidt, C.L.10
-
37
-
-
61449267734
-
Structures of falcipain-2 and falcipain- 3 bound to small molecule inhibitors: Implications for substrate specificity
-
Kerr, I.D.; Lee, J.H.; Pandey, K.C.; Harrison, A.; Sajid, M.; Rosenthal, P.J.; Brinen, L.S. Structures of falcipain-2 and falcipain- 3 bound to small molecule inhibitors: implications for substrate specificity. J. Med. Chem., 2009, 52, 852-857.
-
(2009)
J. Med. Chem.
, vol.52
, pp. 852-857
-
-
Kerr, I.D.1
Lee, J.H.2
Pandey, K.C.3
Harrison, A.4
Sajid, M.5
Rosenthal, P.J.6
Brinen, L.S.7
-
38
-
-
34248154849
-
The Structure of Chagasin in Complex with a Cysteine Protease Clarifies the Binding Mode and Evolution of an Inhibitor Family
-
DOI 10.1016/j.str.2007.03.012, PII S0969212607001207
-
Wang, S.X.; Pandey, K.C.; Scharfstein, J.; Whisstock, J.; Huang, R.K.; Jacobelli, J.; Fletterick, R.J.; Rosenthal, P.J.; Abrahamson, M.; Brinen, L.S.; Rossi, A.; Sali, A.; McKerrow, J.H. The structure of chagasin in complex with a cysteine protease clarifies the binding mode and evolution of an inhibitor family. Structure, 2007,15, 535-543. (Pubitemid 46705555)
-
(2007)
Structure
, vol.15
, Issue.5
, pp. 535-543
-
-
Wang, S.X.1
Pandey, K.C.2
Scharfstein, J.3
Whisstock, J.4
Huang, R.K.5
Jacobelli, J.6
Fletterick, R.J.7
Rosenthal, P.J.8
Abrahamson, M.9
Brinen, L.S.10
Rossi, A.11
Sali, A.12
McKerrow, J.H.13
-
39
-
-
33746791205
-
Structural basis for unique mechanisms of folding and hemoglobin binding by a malarial protease
-
Wang, S.X.; Pendey, K.C.; Somoza, J.R.; Sijwali, P.S.; Kortemme, T.; Brinen, L.S.; Fletterick, R.J.; Rosenthal, P.J.; McKerrow, J.H. Structural basis for unique mechanisms of folding and hemoglobin binding by a malarial protease. Proc. Natl. Acad. Sci. USA, 2006, 103, 11503-11508.
-
(2006)
Proc. Natl. Acad. Sci. USA
, vol.103
, pp. 11503-11508
-
-
Wang, S.X.1
Pendey, K.C.2
Somoza, J.R.3
Sijwali, P.S.4
Kortemme, T.5
Brinen, L.S.6
Fletterick, R.J.7
Rosenthal, P.J.8
McKerrow, J.H.9
-
40
-
-
32644476297
-
Plasmodium falciparum: Biochemical characterization of the cysteine protease falcipain-2'
-
DOI 10.1016/j.exppara.2005.10.007, PII S0014489405002808
-
Singh, N.; Sijwali, P.S.; Pandey, K.C.; Rosenthal, P.J. Plasmodium falciparum: biochemical characterization of the cysteine protease falcipain-2'. Exp. Parasitol., 2006, 112, 187-192. (Pubitemid 43247780)
-
(2006)
Experimental Parasitology
, vol.112
, Issue.3
, pp. 187-192
-
-
Singh, N.1
Sijwali, P.S.2
Pandey, K.C.3
Rosenthal, P.J.4
-
41
-
-
0025964131
-
Reversible binding of peptide aldehydes to papain. Structure-activity relationships
-
Hanzlik, R.P.; Jacober, S.P.; Zygmunt, J. Reversible binding of peptide aldehydes to papain. Structure-activity relationships. Biochim. Biophys. Acta, 1991, 1073, 33-42.
-
(1991)
Biochim. Biophys. Acta
, vol.1073
, pp. 33-42
-
-
Hanzlik, R.P.1
Jacober, S.P.2
Zygmunt, J.3
-
42
-
-
0025102977
-
Inhibition of cathepsin B and papain by peptidyl alpha-keto esters, alpha-keto amides, alpha-diketones, and alpha-keto acids
-
Hu, L.Y.; Abeles, R.H. Inhibition of cathepsin B and papain by peptidyl alpha-keto esters, alpha-keto amides, alpha-diketones, and alpha-keto acids. Arch. Biochem. Biophys., 1990, 281, 271-274.
-
(1990)
Arch. Biochem. Biophys.
, vol.281
, pp. 271-274
-
-
Hu, L.Y.1
Abeles, R.H.2
-
43
-
-
0027424453
-
Peptide alpha-keto ester, alpha-keto amide, and alpha-keto acid inhibitors of calpains and other cysteine proteases
-
Li, Z.; Patil, G.S.; Golubski, Z.E.; Hori, H.; Tehrani, K.; Foreman, J.E.; Eveleth, D.D.; Bartus, R.T.; Powers, J.C. Peptide alpha-keto ester, alpha-keto amide, and alpha-keto acid inhibitors of calpains and other cysteine proteases. J. Med. Chem., 1993, 36, 3472-3480.
-
(1993)
J. Med. Chem.
, vol.36
, pp. 3472-3480
-
-
Li, Z.1
Patil, G.S.2
Golubski, Z.E.3
Hori, H.4
Tehrani, K.5
Foreman, J.E.6
Eveleth, D.D.7
Bartus, R.T.8
Powers, J.C.9
-
44
-
-
0025345455
-
Reversible covalent binding of peptide nitriles to papain
-
Hanzlik, R.P.; Zygmunt, J.; Moon, J.B. Reversible covalent binding of peptide nitriles to papain. Biochim. Biophys. Acta, 1990, 1035,62-70.
-
(1990)
Biochim. Biophys. Acta
, vol.1035
, pp. 62-70
-
-
Hanzlik, R.P.1
Zygmunt, J.2
Moon, J.B.3
-
45
-
-
0022398321
-
Synthesis of peptide fluoromethyl ketones and the inhibition of human cathepsin B
-
Rasnick, D. Synthesis of peptide fluoromethyl ketones and the inhibition of human cathepsin B. Anal. Biochem., 1985, 149, 461-465.
-
(1985)
Anal. Biochem.
, vol.149
, pp. 461-465
-
-
Rasnick, D.1
-
46
-
-
0028269184
-
E64 [trans-epoxysuccinyl-L-leucylamido-(4- Guanidino)butane] analogues as inhibitors of cysteine proteinases: Investigation of S2 subsite interactions
-
Gour-Salin, B.J.; Lachance, P.; Magny, M.C.; Plouffe, C.; Menard, R.; Storer, A.C. E64 [trans-epoxysuccinyl-L-leucylamido-(4- guanidino)butane] analogues as inhibitors of cysteine proteinases: investigation of S2 subsite interactions. Biochem. J., 1994, 299 (Pt2), 389-392.
-
(1994)
Biochem. J.
, vol.299
, Issue.PART2
, pp. 389-392
-
-
Gour-Salin, B.J.1
Lachance, P.2
Magny, M.C.3
Plouffe, C.4
Menard, R.5
Storer, A.C.6
-
47
-
-
0029099619
-
Vinyl Sulfones as Mechanism-Based Cysteine Protease Inhibitors
-
Palmer, J.T.; Rasnick, D.; Klaus, J.L.; Bromme, D. Vinyl Sulfones as Mechanism-Based Cysteine Protease Inhibitors. J. Med. Chem., 1995, 38, 3193-3196.
-
(1995)
J. Med. Chem.
, vol.38
, pp. 3193-3196
-
-
Palmer, J.T.1
Rasnick, D.2
Klaus, J.L.3
Bromme, D.4
-
48
-
-
0025719869
-
Antimalarial effects of peptide inhibitors of a Plasmodium falciparum cysteine proteinase
-
Rosenthal, P.J.; Wollish, W.S.; Palmer, J.T.; Rasnick, D. Antimalarial effects of peptide inhibitors of a Plasmodium falciparum cysteine proteinase. J. Clin. Invest., 1991, 88, 1467-1472.
-
(1991)
J. Clin. Invest.
, vol.88
, pp. 1467-1472
-
-
Rosenthal, P.J.1
Wollish, W.S.2
Palmer, J.T.3
Rasnick, D.4
-
49
-
-
0027512171
-
Inhibition of a Plasmodium vinckei cysteine proteinase cures murine malaria
-
Rosenthal, P.J.; Lee, G.K.; Smith, R.E. Inhibition of a Plasmodium vinckei cysteine proteinase cures murine malaria. J. Clin. Invest., 1993, 91, 1052-1056.
-
(1993)
J. Clin. Invest.
, vol.91
, pp. 1052-1056
-
-
Rosenthal, P.J.1
Lee, G.K.2
Smith, R.E.3
-
50
-
-
0030011095
-
Antimalarial effects of vinyl sulfone cysteine proteinase inhibitors
-
Rosenthal, P.J.; Olson, J.E.; Lee, G.K.; Palmer, J.T.; Klaus, J.L.; Rasnick, D. Antimalarial effects of vinyl sulfone cysteine proteinase inhibitors. Antimicrob. Agents Chemother., 1996, 40,1600-1603. (Pubitemid 26227342)
-
(1996)
Antimicrobial Agents and Chemotherapy
, vol.40
, Issue.7
, pp. 1600-1603
-
-
Rosenthal, P.J.1
Olson, J.E.2
Lee, G.K.3
Palmer, J.T.4
Klaus, J.L.5
Rasnick, D.6
-
51
-
-
0142142211
-
Cysteine protease inhibitors containing small rings
-
Schirmeister, T.; Klockow, A. Cysteine protease inhibitors containing small rings. Mini-Rev. Med. Chem., 2003, 3, 585-596.
-
(2003)
Mini-Rev. Med. Chem.
, vol.3
, pp. 585-596
-
-
Schirmeister, T.1
Klockow, A.2
-
52
-
-
0024208917
-
A malarial cysteine proteinase is necessary for hemoglobin degradation by Plasmodium falciparum
-
Rosenthal, P.J.; McKerrow, J.H.; Aikawa, M.; Nagasawa, H.; Leech, J.H. A malarial cysteine proteinase is necessary for hemoglobin degradation by Plasmodium falciparum. J. Clin. Invest., 1988, 82, 1560-1566.
-
(1988)
J. Clin. Invest.
, vol.82
, pp. 1560-1566
-
-
Rosenthal, P.J.1
McKerrow, J.H.2
Aikawa, M.3
Nagasawa, H.4
Leech, J.H.5
-
53
-
-
0141509925
-
Selective inhibition of a two-step egress of malaria parasites from the host erythrocyte
-
Wickham, M.E.; Culvenor, J.G.; Cowman, A.F. Selective inhibition of a two-step egress of malaria parasites from the host erythrocyte. J. Biol. Chem., 2003, 278, 37658-37663.
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 37658-37663
-
-
Wickham, M.E.1
Culvenor, J.G.2
Cowman, A.F.3
-
54
-
-
0033057631
-
Antimalarial effects in mice of orally administered peptidyl cysteine protease inhibitors
-
Olson, J.E.; Lee, G.K.; Semenov, A.; Rosenthal, P.J. Antimalarial effects in mice of orally administered peptidyl cysteine protease inhibitors. Bioorg. Med. Chem., 1999, 7, 633-638.
-
(1999)
Bioorg. Med. Chem.
, vol.7
, pp. 633-638
-
-
Olson, J.E.1
Lee, G.K.2
Semenov, A.3
Rosenthal, P.J.4
-
55
-
-
0037226491
-
Structure-activity relationships for inhibition of cysteine protease activity and development of Plasmodium falciparum by peptidyl vinyl sulfones
-
Shenai, B.R.; Lee, B.J.; Alvarez-Hernandez, A.; Chong, P.Y.; Emal, C.D.; Neitz, R.J.; Roush, W.R.; Rosenthal, P.J. Structure-activity relationships for inhibition of cysteine protease activity and development of Plasmodium falciparum by peptidyl vinyl sulfones. Antimicrob. Agents Chemother., 2003, 47, 154-160.
-
(2003)
Antimicrob. Agents Chemother.
, vol.47
, pp. 154-160
-
-
Shenai, B.R.1
Lee, B.J.2
Alvarez-Hernandez, A.3
Chong, P.Y.4
Emal, C.D.5
Neitz, R.J.6
Roush, W.R.7
Rosenthal, P.J.8
-
56
-
-
33745242354
-
Dipeptide vinyl sultams: Synthesis via the Wittig-Horner reaction and activity against papain, falcipain-2 and Plasmodium falciparum
-
Valente, C.; Guedes, R.C.; Moreira, R.; Iley, J.; Gut, J.; Rosenthal, P.J. Dipeptide vinyl sultams: synthesis via the Wittig-Horner reaction and activity against papain, falcipain-2 and Plasmodium falciparum. Bioorg. Med. Chem. Lett., 2006, 16, 4115-4119.
-
(2006)
Bioorg. Med. Chem. Lett.
, vol.16
, pp. 4115-4119
-
-
Valente, C.1
Guedes, R.C.2
Moreira, R.3
Iley, J.4
Gut, J.5
Rosenthal, P.J.6
-
57
-
-
0344875075
-
Antimalarial activities of novel synthetic cysteine protease inhibitors
-
Lee, B.J.; Singh, A.; Chiang, P.; Kemp, S.J.; Goldman, E.A.; Weinhouse, M.I.; Vlasuk, G.P.; Rosenthal, P.J. Antimalarial activities of novel synthetic cysteine protease inhibitors. Antimicrob. Agents Chemother., 2003, 47, 3810-3814.
-
(2003)
Antimicrob. Agents Chemother.
, vol.47
, pp. 3810-3814
-
-
Lee, B.J.1
Singh, A.2
Chiang, P.3
Kemp, S.J.4
Goldman, E.A.5
Weinhouse, M.I.6
Vlasuk, G.P.7
Rosenthal, P.J.8
-
58
-
-
33750947149
-
Synthesis and biological evaluation of phenolic Mannich bases of benzaldehyde and (thio)semicarbazone derivatives against the cysteine protease falcipain-2 and a chloroquine resistant strain of Plasmodium falciparum
-
Chipeleme, A.; Gut, J.; Rosenthal, P.J.; Chibale, K. Synthesis and biological evaluation of phenolic Mannich bases of benzaldehyde and (thio)semicarbazone derivatives against the cysteine protease falcipain-2 and a chloroquine resistant strain of Plasmodium falciparum. Bioorg. Med. Chem., 2007, 15, 273-282.
-
(2007)
Bioorg. Med. Chem.
, vol.15
, pp. 273-282
-
-
Chipeleme, A.1
Gut, J.2
Rosenthal, P.J.3
Chibale, K.4
-
59
-
-
0029130176
-
Aziridine analogs of [[trans-(epoxysuccinyl)-L-leucyl]amino]-4- Guanidinobutane (E-64) as inhibitors of cysteine proteases
-
Martichonok, V.; Plouffe, C.; Storer, A.C.; Menard, R.; Jones, J.B. Aziridine analogs of [[trans-(epoxysuccinyl)-L-leucyl]amino]-4- guanidinobutane (E-64) as inhibitors of cysteine proteases. J. Med. Chem., 1995, 38, 3078-3085.
-
(1995)
J. Med. Chem.
, vol.38
, pp. 3078-3085
-
-
Martichonok, V.1
Plouffe, C.2
Storer, A.C.3
Menard, R.4
Jones, J.B.5
-
60
-
-
37849049518
-
Screening of protease inhibitors as antiplasmodial agents. Part I: Aziridines and epoxides
-
Schulz, F.; Gelhaus, C.; Degel, B.; Vicik, R.; Heppner, S.; Breuning, A.; Leippe, M.; Gut, J.; Rosenthal, P.J.; Schirmeister, T. Screening of protease inhibitors as antiplasmodial agents. Part I: Aziridines and epoxides. Chem. Med. Chem., 2007, 2, 1214-1224.
-
(2007)
Chem. Med. Chem.
, vol.2
, pp. 1214-1224
-
-
Schulz, F.1
Gelhaus, C.2
Degel, B.3
Vicik, R.4
Heppner, S.5
Breuning, A.6
Leippe, M.7
Gut, J.8
Rosenthal, P.J.9
Schirmeister, T.10
-
61
-
-
65749094248
-
Artemisinin-dipeptidyl vinyl sulfone hybrid molecules: Design, synthesis and preliminary SAR for antiplasmodial activity and falcipain-2 inhibition
-
Capela, R.; Oliveira, R.; Goncalves, L.M.; Domingos, A.; Gut, J.; Rosenthal, P.J.; Lopes, F.; Moreira, R. Artemisinin-dipeptidyl vinyl sulfone hybrid molecules: design, synthesis and preliminary SAR for antiplasmodial activity and falcipain-2 inhibition. Bioorg. Med. Chem. Lett., 2009, 19, 3229-3232.
-
(2009)
Bioorg. Med. Chem. Lett.
, vol.19
, pp. 3229-3232
-
-
Capela, R.1
Oliveira, R.2
Goncalves, L.M.3
Domingos, A.4
Gut, J.5
Rosenthal, P.J.6
Lopes, F.7
Moreira, R.8
-
62
-
-
31944445555
-
Design, synthesis and evaluation of trisubstituted thiazoles targeting Plasmodium falciparum cysteine proteases
-
Goud, P.M.; Sheri, A.; Desai, P.V.; Watkins, E.B.; Tekwani, B.; Sabnis, Y.; Gut, J.; Rosenthal, P.J.; Avery, M.A. Design, synthesis and evaluation of trisubstituted thiazoles targeting Plasmodium falciparum cysteine proteases. Med. Chem. Res., 2005, 14, 74-105.
-
(2005)
Med. Chem. Res.
, vol.14
, pp. 74-105
-
-
Goud, P.M.1
Sheri, A.2
Desai, P.V.3
Watkins, E.B.4
Tekwani, B.5
Sabnis, Y.6
Gut, J.7
Rosenthal, P.J.8
Avery, M.A.9
-
63
-
-
47149098176
-
Design and synthesis of novel 2-pyridone peptidomimetic falcipain 2/3 inhibitors
-
Verissimo, E.; Berry, N.; Gibbons, P.; Cristiano, M.L.; Rosenthal, P.J.; Gut, J.; Ward, S.A.; O'Neill, P.M. Design and synthesis of novel 2-pyridone peptidomimetic falcipain 2/3 inhibitors. Bioorg. Med. Chem. Lett., 2008, 18, 4210-4214.
-
(2008)
Bioorg. Med. Chem. Lett.
, vol.18
, pp. 4210-4214
-
-
Verissimo, E.1
Berry, N.2
Gibbons, P.3
Cristiano, M.L.4
Rosenthal, P.J.5
Gut, J.6
Ward, S.A.7
O'Neill, P.M.8
-
64
-
-
33744805804
-
Novel peptidomimetic cysteine protease inhibitors as potential antimalarial agents
-
DOI 10.1021/jm060405f
-
Micale, N.; Kozikowski, A.P.; Ettari, R.; Grasso, S.; Zappala, M.; Jeong, J.J.; Kumar, A.; Hanspal, M.; Chishti, A.H. Novel peptidomimetic cysteine protease inhibitors as potential antimalarial agents. J. Med. Chem., 2006, 49, 3064-3067. (Pubitemid 43830505)
-
(2006)
Journal of Medicinal Chemistry
, vol.49
, Issue.11
, pp. 3064-3067
-
-
Micale, N.1
Kozikowski, A.P.2
Ettari, R.3
Grasso, S.4
Zappala, M.5
Jeong, J.-J.6
Kumar, A.7
Hanspal, M.8
Chishti, A.H.9
-
65
-
-
54849203300
-
Nonpeptidic vinyl and allyl phosphonates as falcipain-2 inhibitors
-
Ettari, R.; Nizi, E.; Di Francesco, M.E.; Micale, N.; Grasso, S.; Zappala, M.; Vicik, R.; Schirmeister, T. Nonpeptidic vinyl and allyl phosphonates as falcipain-2 inhibitors. Chem. Med. Chem., 2008, 3, 1030-1033.
-
(2008)
Chem. Med. Chem.
, vol.3
, pp. 1030-1033
-
-
Ettari, R.1
Nizi, E.2
Di Francesco, M.E.3
Micale, N.4
Grasso, S.5
Zappala, M.6
Vicik, R.7
Schirmeister, T.8
-
66
-
-
0027480452
-
Structure-based inhibitor design by using protein models for the development of antiparasitic agents
-
Ring, C.S.; Sun, E.; McKerrow, J.H.; Lee, G.K.; Rosenthal, P.J.; Kuntz, I.D.; Cohen, F.E. Structure-based inhibitor design by using protein models for the development of antiparasitic agents. Proc. Natl. Acad. Sci. USA, 1993, 90, 3583-3587.
-
(1993)
Proc. Natl. Acad. Sci. USA
, vol.90
, pp. 3583-3587
-
-
Ring, C.S.1
Sun, E.2
McKerrow, J.H.3
Lee, G.K.4
Rosenthal, P.J.5
Kuntz, I.D.6
Cohen, F.E.7
-
67
-
-
0029594562
-
In vitro antimalarial activity of chalcones and their derivatives
-
Li, R.; Chen, X.; Gong, B.; Dominguez, J.N.; Davidson, E.; Kurzban, G.; Miller, R.E.; Nuzum, E.O.; Rosenthal, P.J. In vitro antimalarial activity of chalcones and their derivatives. J. Med. Chem., 1995, 38, 5031-5037. (Pubitemid 26012258)
-
(1995)
Journal of Medicinal Chemistry
, vol.38
, Issue.26
, pp. 5031-5037
-
-
Li, R.1
Kenyon, G.L.2
Cohen, F.E.3
Chen, X.4
Gong, B.5
Dominguez, J.N.6
Davidson, E.7
Kurzban, G.8
Miller, R.E.9
Nuzum, E.O.10
Rosenthal, P.J.11
McKerrow, J.H.12
-
68
-
-
10644241872
-
Identification of novel parasitic cysteine protease inhibitors using virtual screening. 1. the ChemBridge database
-
DOI 10.1021/jm0493717
-
Desai, P.V.; Patny, A.; Sabnis, Y.; Tekwani, B.; Gut, J.; Rosenthal, P.; Srivastava, A.; Avery, M. Identification of novel parasitic cysteine protease inhibitors using virtual screening. 1. the chembridge database. J. Med. Chem., 2004, 47, 6609-6615. (Pubitemid 39657322)
-
(2004)
Journal of Medicinal Chemistry
, vol.47
, Issue.26
, pp. 6609-6615
-
-
Desai, P.V.1
Patny, A.2
Sabnis, Y.3
Tekwani, B.4
Gut, J.5
Rosenthal, P.6
Srivastava, A.7
Avery, M.8
-
69
-
-
33644854957
-
Identification of novel parasitic cysteine protease inhibitors by use of virtual screening. 2. the available chemical directory
-
DOI 10.1021/jm0505765
-
Desai, P.V.; Patny, A.; Gut, J.; Rosenthal, P.J.; Tekwani, B.; Srivastava, A.; Avery, M. Identification of novel parasitic cysteine protease inhibitors by use of virtual screening. 2. the available chemical directory. J. Med. Chem., 2006, 49, 1576-1584. (Pubitemid 43376503)
-
(2006)
Journal of Medicinal Chemistry
, vol.49
, Issue.5
, pp. 1576-1584
-
-
Desai, P.V.1
Patny, A.2
Gut, J.3
Rosenthal, P.J.4
Tekwani, B.5
Srivastava, A.6
Avery, M.7
-
70
-
-
84925567658
-
Identification of novel falcipain-2 inhibitors as potential antimalarial agents through structure-based virtual screening
-
ACS ASAP.
-
Li, H.; Huang, J.; Chen, L.; Liu, X.; Chen, T.; Zhu, J.; Lu, W.; Shen, X.; Li, J.; Hilgenfeld, R.; Jiang, H. Identification of novel falcipain-2 inhibitors as potential antimalarial agents through structure-based virtual screening. J. Med. Chem., ACS ASAP.
-
J. Med. Chem.
-
-
Li, H.1
Huang, J.2
Chen, L.3
Liu, X.4
Chen, T.5
Zhu, J.6
Lu, W.7
Shen, X.8
Li, J.9
Hilgenfeld, R.10
Jiang, H.11
-
71
-
-
23844520095
-
A new rapid and effective chemistry space filter in recognizing a druglike database
-
Zheng, S.; Luo, X.; Chen, G.; Zhu, W.; Shen, J.; Chen, K.; Jiang, H. A new rapid and effective chemistry space filter in recognizing a druglike database. J. Chem. Inf. Model., 2005, 45, 856-862.
-
(2005)
J. Chem. Inf. Model.
, vol.45
, pp. 856-862
-
-
Zheng, S.1
Luo, X.2
Chen, G.3
Zhu, W.4
Shen, J.5
Chen, K.6
Jiang, H.7
-
72
-
-
61449142511
-
2-(3,4-dihydro-4-oxothieno[2,3-d]pyrimidin-2-ylthio) acetamides as a new class of falcipain-2 Inhibitors. 3. Design, synthesis and biological evaluation
-
Zhu, J.; Chen, T.; Liu, J.; Ma, R.; Lu, W.; Huang, J.; Li, H.; Li, J.; Jiang, H. 2-(3,4-dihydro-4-oxothieno[2,3-d]pyrimidin-2-ylthio) acetamides as a new class of falcipain-2 Inhibitors. 3. Design, synthesis and biological evaluation. Molecules, 2009, 14, 785-797.
-
(2009)
Molecules
, vol.14
, pp. 785-797
-
-
Zhu, J.1
Chen, T.2
Liu, J.3
Ma, R.4
Lu, W.5
Huang, J.6
Li, H.7
Li, J.8
Jiang, H.9
-
73
-
-
59349095066
-
2-amido-3-(1H-indol-3-yl)-N-substitued-propanamides as a new class of falcipain-2 inhibitors. 1. Design, synthesis, biological evaluation and binding model studies
-
Zhu, J.; Chen, T.; Chen, L.; Lu, W.; Che, P.; Huang, J.; Li, H.; Li, J.; Jiang, H. 2-amido-3-(1H-indol-3-yl)-N-substitued-propanamides as a new class of falcipain-2 inhibitors. 1. Design, synthesis, biological evaluation and binding model studies. Molecules, 2009,14, 494-508.
-
(2009)
Molecules
, vol.14
, pp. 494-508
-
-
Zhu, J.1
Chen, T.2
Chen, L.3
Lu, W.4
Che, P.5
Huang, J.6
Li, H.7
Li, J.8
Jiang, H.9
-
74
-
-
33644854957
-
Identification of novel parasitic cysteine protease inhibitors by use of virtual screening. 2. the available chemical directory
-
DOI 10.1021/jm0505765
-
Desai, P.V.; Patny, A.; Gut, J.; Rosenthal, P.J.; Tekwani, B.; Srivastava, A.; Avery, M. Identification of novel parasitic cysteine protease inhibitors by use of virtual screening. 2. the available chemical directory. J. Med. Chem., 2006, 49, 1576-1584. (Pubitemid 43376503)
-
(2006)
Journal of Medicinal Chemistry
, vol.49
, Issue.5
, pp. 1576-1584
-
-
Desai, P.V.1
Patny, A.2
Gut, J.3
Rosenthal, P.J.4
Tekwani, B.5
Srivastava, A.6
Avery, M.7
-
75
-
-
0028357495
-
Licochalcone A, a new antimalarial agent, inhibits in vitro growth of the human malaria parasite Plasmodium falciparum and protects mice from P. yoelii infection
-
Chen, M.; Theander, T.G.; Christensen, S.B.; Hviid, L.; Zhai, L.; Kharazmi, A. Licochalcone A, a new antimalarial agent, inhibits in vitro growth of the human malaria parasite Plasmodium falciparum and protects mice from P. yoelii infection. Antimicrob. Agents Chemother., 1994, 38, 1470-1475.
-
(1994)
Antimicrob. Agents Chemother.
, vol.38
, pp. 1470-1475
-
-
Chen, M.1
Theander, T.G.2
Christensen, S.B.3
Hviid, L.4
Zhai, L.5
Kharazmi, A.6
-
76
-
-
0035357889
-
Synthesis of quinolinyl chalcones and evaluation of their antimalarial activity
-
DOI 10.1016/S0223-5234(01)01245-4, PII S0223523401012454
-
Dominguez, J.N.; Charris, J.E.; Lobo, G.; Gamboa de Dominguez, N.; Moreno, M.M.; Riggione, F.; Sanchez, E.; Olson, J.; Rosenthal, P.J. Synthesis of quinolinyl chalcones and evaluation of their antimalarial activity. Eur. J. Med. Chem., 2001, 36, 555-560. (Pubitemid 32781719)
-
(2001)
European Journal of Medicinal Chemistry
, vol.36
, Issue.6
, pp. 555-560
-
-
Dominguez, J.N.1
Charris, J.E.2
Lobo, G.3
Gamboa De Dominguez, N.4
Moreno, M.M.5
Riggione, F.6
Sanchez, E.7
Olson, J.8
Rosenthal, P.J.9
-
77
-
-
0035818913
-
Antimalarial alkoxylated and hydroxylated chalcones [corrected]: Structure-activity relationship analysis
-
Liu, M.; Wilairat, P.; Go, M.L. Antimalarial alkoxylated and hydroxylated chalcones [corrected]: structure-activity relationship analysis. J. Med. Chem., 2001, 44, 4443-4452.
-
(2001)
J. Med. Chem.
, vol.44
, pp. 4443-4452
-
-
Liu, M.1
Wilairat, P.2
Go, M.L.3
-
78
-
-
18644361984
-
Synthesis and evaluation of new antimalarial phenylurenyl chalcone derivatives
-
DOI 10.1021/jm058208o
-
Dominguez, J.N.; Leon, C.; Rodrigues, J.; Gamboa de Dominguez, N.; Gut, J.; Rosenthal, P.J. Synthesis and evaluation of new antimalarial phenylurenyl chalcone derivatives. J. Med. Chem., 2005, 48, 3654-3658. (Pubitemid 40664115)
-
(2005)
Journal of Medicinal Chemistry
, vol.48
, Issue.10
, pp. 3654-3658
-
-
Dominguez, J.N.1
Leon, C.2
Rodrigues, J.3
De Dominguez, N.G.4
Gut, J.5
Rosenthal, P.J.6
-
79
-
-
0034694354
-
Parallel synthesis of isatin-based serine protease inhibitors
-
Shuttleworth, S.J.; Nasturica, D.; Gervais, C.; Siddiqui, M.A.; Rando, R.F.; Lee, N. Parallel synthesis of isatin-based serine protease inhibitors. Bioorg. Med. Chem. Lett., 2000, 10, 2501-2504.
-
(2000)
Bioorg. Med. Chem. Lett.
, vol.10
, pp. 2501-2504
-
-
Shuttleworth, S.J.1
Nasturica, D.2
Gervais, C.3
Siddiqui, M.A.4
Rando, R.F.5
Lee, N.6
-
80
-
-
12644306888
-
Design, synthesis, and evaluation of nonpeptidic inhibitors of human rhinovirus 3C protease
-
DOI 10.1021/jm960603e
-
Webber, S.E.; Tikhe, J.; Worland, S.T.; Fuhrman, S.A.; Hendrickson, T.F.; Matthews, D.A.; Love, R.A.; Patick, A.K.; Meador, J.W.; Ferre, R.A.; Brown, E.L.; DeLisle, D.M.; Ford, C.E.; Binford, S.L. Design, synthesis, and evaluation of nonpeptidic inhibitors of human rhinovirus 3C protease. J. Med. Chem., 1996, 39, 5072-5082. (Pubitemid 27008954)
-
(1996)
Journal of Medicinal Chemistry
, vol.39
, Issue.26
, pp. 5072-5082
-
-
Webber, S.E.1
Tikhe, J.2
Worland, S.T.3
Fuhrman, S.A.4
Hendrickson, T.F.5
Matthews, D.A.6
Love, R.A.7
Patick, A.K.8
Meador, J.W.9
Ferre, R.A.10
Brown, E.L.11
DeLisle, D.M.12
Ford, C.E.13
Binford, S.L.14
-
81
-
-
0141627969
-
Synthesis and evaluation of isatins and thiosemicarbazone derivatives against cruzain, falcipain-2 and rhodesain
-
Chiyanzu, I.; Hansell, E.; Gut, J.; Rosenthal, P.J.; McKerrow, J.H.; Chibale, K. Synthesis and evaluation of isatins and thiosemicarbazone derivatives against cruzain, falcipain-2 and rhodesain. Bioorg. Med. Chem. Lett., 2003, 13, 3527-3530.
-
(2003)
Bioorg. Med. Chem. Lett.
, vol.13
, pp. 3527-3530
-
-
Chiyanzu, I.1
Hansell, E.2
Gut, J.3
Rosenthal, P.J.4
McKerrow, J.H.5
Chibale, K.6
-
82
-
-
9644265257
-
Discovery of potent thiosemicarbazone inhibitors of rhodesain and cruzain
-
DOI 10.1016/j.bmcl.2004.10.023, PII S0960894X0401251X
-
Fujii, N.; Mallari, J.P.; Hansell, E.J.; Mackey, Z.; Doyle, P.; Zhou, Y.M.; Gut, J.; Rosenthal, P.J.; McKerrow, J.H.; Guy, R.K. Discovery of potent thiosemicarbazone inhibitors of rhodesain and cruzain. Bioorg. Med. Chem. Lett., 2005, 15, 121-123. (Pubitemid 39575795)
-
(2005)
Bioorganic and Medicinal Chemistry Letters
, vol.15
, Issue.1
, pp. 121-123
-
-
Fujii, N.1
Mallari, J.P.2
Hansell, E.J.3
MacKey, Z.4
Doyle, P.5
Zhou, Y.M.6
Gut, J.7
Rosenthal, P.J.8
McKerrow, J.H.9
Guy, R.K.10
-
83
-
-
0013074820
-
A major outbreak of severe acute respiratory syndrome in Hong Kong
-
DOI 10.1056/NEJMoa030685
-
Lee, N.; Hui, D.; Wu, A.; Chan, P.; Cameron, P.; Joynt, G.M.; Ahuja, A.; Yung, M.Y.; Leung, C.B.; To, K.F.; Lui, S.F.; Szeto, C.C.; Chung, S.; Sung, J.J. A major outbreak of severe acute respiratory syndrome in Hong Kong. N. Engl. J. Med., 2003, 348,1986-1994. (Pubitemid 36569987)
-
(2003)
New England Journal of Medicine
, vol.348
, Issue.20
, pp. 1986-1994
-
-
Lee, N.1
Hui, D.2
Wu, A.3
Chan, P.4
Cameron, P.5
Joynt, G.M.6
Ahuja, A.7
Yung, M.Y.8
Leung, C.B.9
To, K.F.10
Lui, S.F.11
Szeto, C.C.12
Chung, S.13
Sung, J.J.Y.14
-
84
-
-
0013165966
-
Identification of severe acute respiratory syndrome in Canada
-
DOI 10.1056/NEJMoa030634
-
Poutanen, S.M.; Low, D.E.; Henry, B.; Finkelstein, S.; Rose, D.; Green, K.; Tellier, R.; Draker, R.; Adachi, D.; Ayers, M.; Chan, A.K.; Skowronski, D.M.; Salit, I.; Simor, A.E.; Slutsky, A.S.; Doyle, P.W.; Krajden, M.; Petric, M.; Brunham, R.C.; McGeer, A.J. Identification of severe acute respiratory syndrome in Canada. N. Engl. J. Med., 2003, 348, 1995-2005. (Pubitemid 36569988)
-
(2003)
New England Journal of Medicine
, vol.348
, Issue.20
, pp. 1995-2005
-
-
Poutanen, S.M.1
Low, D.E.2
Henry, B.3
Finkelstein, S.4
Rose, D.5
Green, K.6
Tellier, R.7
Draker, R.8
Adachi, D.9
Ayers, M.10
Chan, A.K.11
Skowronski, D.M.12
Salit, I.13
Simor, A.E.14
Slutsky, A.S.15
Doyle, P.W.16
Krajden, M.17
Petric, M.18
Brunham, R.C.19
McGeer, A.J.20
more..
-
85
-
-
0013255608
-
A cluster of cases of severe acute respiratory syndrome in Hong Kong
-
DOI 10.1056/NEJMoa030666
-
Tsang, K.W.; Ho, P.L.; Ooi, G.C.; Yee, W.K.; Wang, T.; Chan-Yeung, M.; Lam, W.K.; Seto, W.H.; Yam, L.Y.; Cheung, T.M.; Wong, P.C.; Lam, B.; Ip, M.S.; Chan, J.; Yuen, K.Y.; Lai, K.N. A cluster of cases of severe acute respiratory syndrome in Hong Kong. N. Engl. J. Med., 2003, 348, 1977-1985. (Pubitemid 36569986)
-
(2003)
New England Journal of Medicine
, vol.348
, Issue.20
, pp. 1977-1985
-
-
Tsang, K.W.1
Ho, P.L.2
Ooi, G.C.3
Yee, W.K.4
Wang, T.5
Chan-Yeung, M.6
Lam, W.K.7
Seto, W.H.8
Yam, L.Y.9
Cheung, T.M.10
Wong, P.C.11
Lam, B.12
Ip, M.S.13
Chan, J.14
Yuen, K.Y.15
Lai, K.N.16
-
86
-
-
84925570813
-
-
Global Alert and Response (GAR), [Access date: August8, 2009].
-
Global Alert and Response (GAR), http://www.who.int/csr/sars/country/ table2004-04-21/en/index.html [Access date: August8, 2009].
-
-
-
-
87
-
-
0042198682
-
Newly discovered coronavirus as the primary cause of severe acute respiratory syndrome
-
DOI 10.1016/S0140-6736(03)13967-0
-
Kuiken, T.; Fouchier, R.A.M.; Schutten, M.; Rimmelzwaan, G.F.; van Amerongen, G.; van Riel, D.; Laman, J.D.; de Jong, T.; van Doornum, G.; Lim, W.; Ling, A.E.; Chan, P.K.S.; Tam, J.S.; Zambon, M.C.; Gopal, R.; Drosten, C.; van der Werf, S.; Escriou, N.; Manuguerra, J.-C.; Stohr, K.; Peiris, J.S.M.; Osterhaus, A.D.M.E. Newly discovered coronavirus as the primary cause of severe acute respiratory syndrome. Lancet, 2003, 362, 263-270. (Pubitemid 36936836)
-
(2003)
Lancet
, vol.362
, Issue.9380
, pp. 263-270
-
-
Kuiken, T.1
Fouchier, R.A.M.2
Schutten, M.3
Rimmelzwaan, G.F.4
Van Amerongen, G.5
Van Riel, D.6
Laman, J.D.7
De Jong, T.8
Van Doornum, G.9
Lim, W.10
Ling, A.E.11
Chan, P.K.S.12
Tam, J.S.13
Zambon, M.C.14
Gopal, R.15
Drosten, C.16
Van Der Werf, S.17
Escriou, N.18
Manuguerra, J.-C.19
Stohr, K.20
Peiris, J.S.M.21
Osterhaus, A.D.M.E.22
more..
-
88
-
-
0038076030
-
A novel coronavirus associated with severe acute respiratory syndrome
-
DOI 10.1056/NEJMoa030781
-
Ksiazek, T.G.; Erdman, D.; Goldsmith, C.S.; Zaki, S.R.; Peret, T.; Emery, S.; Tong, S.; Urbani, C.; Comer, J.A.; Lim, W.; Rollin, P.E.; Dowell, S.F.; Ling, A.-E.; Humphrey, C.D.; Shieh, W.-J.; Guarner, J.; Paddock, C.D.; Rota, P.; Fields, B.; DeRisi, J.; Yang, J.-Y.; Cox, N.; Hughes, J.M.; LeDuc, J.W.; Bellini, W.J.; Anderson, L.J.; Cannon, A.D.L.; Curtis, M.; Farrar, B.; Morgan, L.; Pezzanite, L.; Sanchez, A.J.; Slaughter, K.A.; Stevens, T.L.; Stockton, P.C.; Wagoner, K.D.; Sanchez, A.; Nichol, S.; Vincent, M.; Osborne, J.; Honig, J.; Brickson, B.R.; Holloway, B.; McCaustland, K.; Lingappa, J.; Lowe, L.; Scott, S.; Lu, X.; Villamarzo, Y.; Cook, B.; Chen, Q.; Birge, C.; Shu, B.; Pallansch, M.; Tatti, K.M.; Morken, T.; Smith, C.; Greer, P.; White, E.; McGlothen, T.; Bhatnagar, J.; Patel, M.; Bartlett, J.; Montague, J.; Lee, W.; Packard, M.; Thompson, H.A.; Moen, A.; Fukuda, K.; Uyeki, T.; Harper, S.; Klimov, A.; Lindstrom, S.; Benson, R.; Carlone, G.; Facklam, R.; Fields, P.; Levett, P.; Mayer, L.; Talkington, D.; Thacker, W.L.; Tondella, M.L.C.; Whitney, C.; Robertson, B.; Warnock, D.; Brooks, T.; Schrag, S.; Rosenstein, N.; Arthur, R.; Ganem, D.; Poutanen, S.M.; Chen, T.J.; Hsiao, C.H.; Wai-Fu, N.G.; Ho, M.; Keung, T.K.; Nghiem, K.H.; Nguyen, H.K.L.; Le, M.Q.; Nguyen, H.H.T.; Hoang, L.T.; Vu, T.H.; Vu, H.Q.; Chunsuttiwat, S. A novel coronavirus associated with severe acute respiratory syndrome. N. Engl. J. Med., 2003, 348, 1953-1966. (Pubitemid 36569984)
-
(2003)
New England Journal of Medicine
, vol.348
, Issue.20
, pp. 1953-1966
-
-
Ksiazek, T.G.1
Erdman, D.2
Goldsmith, C.S.3
Zaki, S.R.4
Peret, T.5
Emery, S.6
Tong, S.7
Urbani, C.8
Comer, J.A.9
Lim, W.10
Rollin, P.E.11
Dowell, S.F.12
Ling, A.-E.13
Humphrey, C.D.14
Shieh, W.-J.15
Guarner, J.16
Paddock, C.D.17
Roca, P.18
Fields, B.19
Derisi, J.20
Yang, J.-Y.21
Cox, N.22
Hughes, J.M.23
Leduc, J.W.24
Bellini, W.J.25
Anderson, L.J.26
more..
-
89
-
-
0042427333
-
Severe acute respiratory syndrome: Identification of the etiological agent
-
DOI 10.1016/S1471-4914(03)00133-3
-
Drosten, C.; Preiser, W.; Gunther, S.; Schmitz, H.; Doerr, H.W. Severe acute respiratory syndrome: identification of the etiological agent. Trends Mol. Med., 2003, 9, 325-327. (Pubitemid 37040026)
-
(2003)
Trends in Molecular Medicine
, vol.9
, Issue.8
, pp. 325-327
-
-
Drosten, C.1
Preiser, W.2
Gunther, S.3
Schmitz, H.4
Doerr, H.W.5
-
90
-
-
0042377358
-
Mechanisms and enzymes involved in SARS coronavirus genome expression
-
DOI 10.1099/vir.0.19424-0
-
Thiel, V.; Ivanov, K.A.; Putics, A.; Hertzig, T.; Schelle, B.; Bayer, S.; Weissbrich, B.; Snijder, E.J.; Rabenau, H.; Doerr, H.W.; Gorbalenya, A.E.; Ziebuhr, J. Mechanisms and enzymes involved in SARS coronavirus genome expression. J. Gen. Virol., 2003, 84,2305-2315. (Pubitemid 37063118)
-
(2003)
Journal of General Virology
, vol.84
, Issue.9
, pp. 2305-2315
-
-
Thiel, V.1
Ivanov, K.A.2
Putics, A.3
Hertzig, T.4
Schelle, B.5
Bayer, S.6
Weissbrich, B.7
Snijder, E.J.8
Rabenau, H.9
Doerr, H.W.10
Gorbalenya, A.E.11
Ziebuhr, J.12
-
91
-
-
24744432305
-
Mechanism of the maturation process of SARS-CoV 3CL protease
-
Hsu, M.-F.; Kuo, C.-J.; Chang, K.-T.; Chang, H.-C.; Chou, C.-C.; Ko, T.-P.; Shr, H.-L.; Chang, G.-G.; Wang, A.H.J.; Liang, P.-H. Mechanism of the maturation process of SARS-CoV 3CL protease. J. Biol. Chem., 2005, 280, 31257-31266.
-
(2005)
J. Biol. Chem.
, vol.280
, pp. 31257-31266
-
-
Hsu, M.-F.1
Kuo, C.-J.2
Chang, K.-T.3
Chang, H.-C.4
Chou, C.-C.5
Ko, T.-P.6
Shr, H.-L.7
Chang, G.-G.8
Wang, A.H.J.9
Liang, P.-H.10
-
92
-
-
0034072633
-
Virus-encoded proteinases and proteolytic processing in the nidovirales
-
Ziebuhr, J.; Snijder, E.J.; Gorbalenya, A.E. Virus-encoded proteinases and proteolytic processing in the nidovirales. J. Gen. Virol., 2000, 81, 853-879.
-
(2000)
J. Gen. Virol.
, vol.81
, pp. 853-879
-
-
Ziebuhr, J.1
Snijder, E.J.2
Gorbalenya, A.E.3
-
93
-
-
0030970783
-
Biosynthesis, purification, and characterization of the human coronavirus 229E 3C-like proteinase
-
Ziebuhr, J.; Heusipp, G.; Siddell, S.G. Biosynthesis, purification, and characterization of the human coronavirus 229E 3C-like proteinase. J. Virol., 1997, 71, 3992-3997. (Pubitemid 27172414)
-
(1997)
Journal of Virology
, vol.71
, Issue.5
, pp. 3992-3997
-
-
Ziebuhr, J.1
Heusipp, G.2
Siddell, S.G.3
-
94
-
-
12444278968
-
A 3D model of SARS-CoV 3CL proteinase and its inhibitors design by virtual screening
-
Xiong, B.; Gui, C.-S.; Xu, X.-Y.; Luo, C.; Chen, J.; Luo, H.-B.; Chen, L.-L.; Li, G.-W.; Sun, T.; Yu, C.-Y.; Yue, L.-D.; Duan, W.-H.; Shen, J.-K.; Qin, L.; Shi, T.-L.; Li, Y.-X.; Chen, K.-X.; Luo, X.-M.; Shen, X.; Shen, J.-H.; Jiang, H.-L. A 3D model of SARS-CoV 3CL proteinase and its inhibitors design by virtual screening. Acta Pharmacol. Sin., 2003, 24, 497-504.
-
(2003)
Acta Pharmacol. Sin.
, vol.24
, pp. 497-504
-
-
Xiong, B.1
Gui, C.-S.2
Xu, X.-Y.3
Luo, C.4
Chen, J.5
Luo, H.-B.6
Chen, L.-L.7
Li, G.-W.8
Sun, T.9
Yu, C.-Y.10
Yue, L.-D.11
Duan, W.-H.12
Shen, J.-K.13
Qin, L.14
Shi, T.-L.15
Li, Y.-X.16
Chen, K.-X.17
Luo, X.-M.18
Shen, X.19
Shen, J.-H.20
Jiang, H.-L.21
more..
-
95
-
-
45449096521
-
Development of broad-spectrum halomethyl ketone inhibitors against coronavirus main protease 3CL(pro)
-
Bacha, U.; Barrila, J.; Gabelli, S.B.; Kiso, Y.; Mario Amzel, L.; Freire, E. Development of broad-spectrum halomethyl ketone inhibitors against coronavirus main protease 3CL(pro). Chem. Biol. Drug Des., 2008, 72, 34-49.
-
(2008)
Chem. Biol. Drug Des.
, vol.72
, pp. 34-49
-
-
Bacha, U.1
Barrila, J.2
Gabelli, S.B.3
Kiso, Y.4
Mario Amzel, L.5
Freire, E.6
-
96
-
-
27444437908
-
Design and synthesis of peptidomimetic severe acute respiratory syndrome chymotrypsin-like protease inhibitors
-
DOI 10.1021/jm050548m
-
Ghosh, A.K.; Xi, K.; Ratia, K.; Santarsiero, B.D.; Fu, W.; Harcourt, B.H.; Rota, P.A.; Baker, S.C.; Johnson, M.E.; Mesecar, A.D. Design and synthesis of peptidomimetic severe acute respiratory syndrome chymotrypsin-like protease inhibitors. J. Med. Chem., 2005, 48, 6767-6771. (Pubitemid 41533095)
-
(2005)
Journal of Medicinal Chemistry
, vol.48
, Issue.22
, pp. 6767-6771
-
-
Ghosh, A.K.1
Xi, K.2
Ratia, K.3
Santarsiero, B.D.4
Fu, W.5
Harcourt, B.H.6
Rota, P.A.7
Baker, S.C.8
Johnson, M.E.9
Mesecar, A.D.10
-
97
-
-
33846637686
-
Crystal structures reveal an induced-fit binding of a substrate-like Aza-peptide epoxide to SARS coronavirus main peptidase
-
Lee, T.W.; Cherney, M.M.; Liu, J.; James, K.E.; Powers, J.C.; Eltis, L.D.; James, M.N. Crystal structures reveal an induced-fit binding of a substrate-like Aza-peptide epoxide to SARS coronavirus main peptidase. J. Mol. Biol., 2007, 366, 916-932.
-
(2007)
J. Mol. Biol.
, vol.366
, pp. 916-932
-
-
Lee, T.W.1
Cherney, M.M.2
Liu, J.3
James, K.E.4
Powers, J.C.5
Eltis, L.D.6
James, M.N.7
-
98
-
-
27344443434
-
PH-dependent Conformational flexibility of the SARS-CoV main proteinase (Mpro) dimer: Molecular dynamics simulations and multiple x-ray structure analyses
-
Tan, J.; Verschueren, K.H.G.; Anand, K.; Shen, J.; Yang, M.; Xu, Y.; Rao, Z.; Bigalke, J.; Heisen, B.; Mesters, J.R.; Chen, K.; Shen, X.; Jiang, H.; Hilgenfeld, R. pH-dependent Conformational flexibility of the SARS-CoV main proteinase (Mpro) dimer: molecular dynamics simulations and multiple x-ray structure analyses. J. Mol. Biol., 2005, 354, 25-40.
-
(2005)
J. Mol. Biol.
, vol.354
, pp. 25-40
-
-
Tan, J.1
Verschueren, K.H.G.2
Anand, K.3
Shen, J.4
Yang, M.5
Xu, Y.6
Rao, Z.7
Bigalke, J.8
Heisen, B.9
Mesters, J.R.10
Chen, K.11
Shen, X.12
Jiang, H.13
Hilgenfeld, R.14
-
99
-
-
44949215788
-
A structural view of the inactivation of the SARS coronavirus main proteinase by benzotriazole esters
-
Verschueren, K.H.; Pumpor, K.; Anemuller, S.; Chen, S.; Mesters, J.R.; Hilgenfeld, R. A structural view of the inactivation of the SARS coronavirus main proteinase by benzotriazole esters. Chem. Biol., 2008, 15, 597-606.
-
(2008)
Chem. Biol.
, vol.15
, pp. 597-606
-
-
Verschueren, K.H.1
Pumpor, K.2
Anemuller, S.3
Chen, S.4
Mesters, J.R.5
Hilgenfeld, R.6
-
100
-
-
33744470114
-
2 crystallographic dimer
-
DOI 10.1107/S1744309105033257
-
Xu, T.; Ooi, A.; Lee, H.C.; Wilmouth, R.; Liu, D.X.; Lescar, J. Structure of the SARS coronavirus main proteinase as an active C2 crystallographic dimer. Acta Crystallogr. Sect F Struct. Biol. Cryst. Commun., 2005, 61, 964-966. (Pubitemid 44210728)
-
(2005)
Acta Crystallographica Section F: Structural Biology and Crystallization Communications
, vol.61
, Issue.11
, pp. 964-966
-
-
Xu, T.1
Ooi, A.2
Lee, H.C.3
Wilmouth, R.4
Liu, D.X.5
Lescar, J.6
-
101
-
-
39749091131
-
Structures of two coronavirus main proteases: Implications for substrate binding and antiviral drug design
-
Xue, X.; Yu, H.; Yang, H.; Xue, F.; Wu, Z.; Shen, W.; Li, J.; Zhou, Z.; Ding, Y.; Zhao, Q.; Zhang, X.C.; Liao, M.; Bartlam, M.; Rao, Z. Structures of two coronavirus main proteases: implications for substrate binding and antiviral drug design. J. Virol., 2008, 82,2515-2527.
-
(2008)
J. Virol.
, vol.82
, pp. 2515-2527
-
-
Xue, X.1
Yu, H.2
Yang, H.3
Xue, F.4
Wu, Z.5
Shen, W.6
Li, J.7
Zhou, Z.8
Ding, Y.9
Zhao, Q.10
Zhang, X.C.11
Liao, M.12
Bartlam, M.13
Rao, Z.14
-
102
-
-
26444498493
-
Design of wide-spectrum inhibitors targeting Coronavirus main proteases
-
Yang, H.; Xie, W.; Xue, X.; Yang, K.; Ma, J.; Liang, W.; Zhao, Q.; Zhou, Z.; Pei, D.; Ziebuhr, J.; Hilgenfeld, R.; Yuen, K.Y.; Wong, L.; Gao, G.; Chen, S.; Chen, Z.; Ma, D.; Bartlam, M.; Rao, Z. Design of wide-spectrum inhibitors targeting Coronavirus main proteases. PLoS Biol., 2005, 3, 1742-1752.
-
(2005)
PLoS Biol.
, vol.3
, pp. 1742-1752
-
-
Yang, H.1
Xie, W.2
Xue, X.3
Yang, K.4
Ma, J.5
Liang, W.6
Zhao, Q.7
Zhou, Z.8
Pei, D.9
Ziebuhr, J.10
Hilgenfeld, R.11
Yuen, K.Y.12
Wong, L.13
Gao, G.14
Chen, S.15
Chen, Z.16
Ma, D.17
Bartlam, M.18
Rao, Z.19
-
103
-
-
0345255626
-
The crystal structures of severe acute respiratory syndrome virus main protease and its complex with an inhibitor
-
DOI 10.1073/pnas.1835675100
-
Yang, H.; Yang, M.; Ding, Y.; Liu, Y.; Lou, Z.; Zhou, Z.; Sun, L.; Mo, L.; Ye, S.; Pang, H.; Gao, G.F.; Anand, K.; Bartlam, M.; Hilgenfeld, R.; Rao, Z. The crystal structures of severe acute respiratory syndrome virus main protease and its complex with an inhibitor. Proc. Natl. Acad. Sci. USA, 2003, 100, 13190-13195. (Pubitemid 37444717)
-
(2003)
Proceedings of the National Academy of Sciences of the United States of America
, vol.100
, Issue.23
, pp. 13190-13195
-
-
Yang, H.1
Yang, M.2
Ding, Y.3
Liu, Y.4
Lou, Z.5
Zhou, Z.6
Sun, L.7
Mo, L.8
Ye, S.9
Pang, H.10
Gao, G.F.11
Anand, K.12
Bartlam, M.13
Hilgenfeld, R.14
Rao, Z.15
-
104
-
-
34547137203
-
A mechanistic view of enzyme inhibition and peptide hydrolysis in the active site of the SARSCoV 3C-like peptidase
-
Yin, J.; Niu, C.; Cherney, M.M.; Zhang, J.; Huitema, C.; Eltis, L.D.; Vederas, J.C.; James, M.N. A mechanistic view of enzyme inhibition and peptide hydrolysis in the active site of the SARSCoV 3C-like peptidase. J. Mol. Biol., 2007, 371, 1060-1074.
-
(2007)
J. Mol. Biol.
, vol.371
, pp. 1060-1074
-
-
Yin, J.1
Niu, C.2
Cherney, M.M.3
Zhang, J.4
Huitema, C.5
Eltis, L.D.6
Vederas, J.C.7
James, M.N.8
-
105
-
-
0036646055
-
Structure of coronavirus main proteinase reveals combination of a chymotrypsin fold with an extra alpha-helical domain
-
DOI 10.1093/emboj/cdf327
-
Anand, K.; Palm, G.J.; Mesters, J.R.; Siddell, S.G.; Ziebuhr, J.; Hilgenfeld, R. Structure of coronavirus main proteinase reveals combination of a chymotrypsin fold with an extra alpha -helical domain. EMBO J., 2002, 21, 3213-3224. (Pubitemid 34760554)
-
(2002)
EMBO Journal
, vol.21
, Issue.13
, pp. 3213-3224
-
-
Anand, K.1
Palm, G.J.2
Mesters, J.R.3
Siddell, S.G.4
Ziebuhr, J.5
Hilgenfeld, R.6
-
106
-
-
33751509079
-
An overall picture of SARS coronavirus (SARS-CoV) genome-encoded major proteins: Structures, functions and drug development
-
Chen, S.; Luo, H.; Chen, L.; Chen, J.; Shen, J.; Zhu, W.; Chen, K.; Shen, X.; Jiang, H. An overall picture of SARS coronavirus (SARS-CoV) genome-encoded major proteins: structures, functions and drug development. Curr. Pharm. Des., 2006, 12, 4539-4553.
-
(2006)
Curr. Pharm. Des.
, vol.12
, pp. 4539-4553
-
-
Chen, S.1
Luo, H.2
Chen, L.3
Chen, J.4
Shen, J.5
Zhu, W.6
Chen, K.7
Shen, X.8
Jiang, H.9
-
107
-
-
2642545063
-
Dissection study on the severe acute respiratory syndrome 3C-like protease reveals the critical role of the extra domain in dimerization of the enzyme. Defining the extra domain as a new target for design of highly specific protease inhibitors
-
DOI 10.1074/jbc.M311744200
-
Shi, J.; Wei, Z.; Song, J. Dissection study on the severe acute respiratory syndrome 3C-like protease reveals the critical role of the extra domain in dimerization of the enzyme: defining the extra domain as a new target for design of highly specific protease inhibitors. J. Biol. Chem., 2004, 279, 24765-24773. (Pubitemid 38725344)
-
(2004)
Journal of Biological Chemistry
, vol.279
, Issue.23
, pp. 24765-24773
-
-
Shi, J.1
Wei, Z.2
Song, J.3
-
108
-
-
18844448391
-
Mutational and inhibitive analysis of SARS coronavirus 3C-like protease by fluorescence resonance energy transfer-based assays
-
DOI 10.1016/j.bbrc.2005.04.072, PII S0006291X05008545
-
Kuang, W.F.; Chow, L.P.; Wu, M.H.; Hwang, L.H. Mutational and inhibitive analysis of SARS coronavirus 3C-like protease by fluorescence resonance energy transfer-based assays. Biochem. Biophys. Res. Commun., 2005, 331, 1554-1559. (Pubitemid 40692532)
-
(2005)
Biochemical and Biophysical Research Communications
, vol.331
, Issue.4
, pp. 1554-1559
-
-
Kuang, W.-F.1
Chow, L.-P.2
Wu, M.-H.3
Hwang, L.-H.4
-
109
-
-
12844272193
-
Severe acute respiratory syndrome coronavirus 3C-like proteinase N terminus is indispensable for proteolytic activity but not for enzyme dimerization: Biochemical and thermodynamic investigation in conjunction with molecular dynamics simulations
-
DOI 10.1074/jbc.M408211200
-
Chen, S.; Chen, L.; Tan, J.; Chen, J.; Du, L.; Sun, T.; Shen, J.; Chen, K.; Jiang, H.; Shen, X. Severe acute respiratory syndrome coronavirus 3C-like proteinase N terminus is indispensable for proteolytic activity but not for enzyme dimerization: biochemical and thermodynamic investigation in conjunction with molecular dynamics simulations. J. Biol. Chem., 2005, 280, 164-173. (Pubitemid 40164977)
-
(2005)
Journal of Biological Chemistry
, vol.280
, Issue.1
, pp. 164-173
-
-
Chen, S.1
Chen, L.2
Tan, J.3
Chen, J.4
Du, L.5
Sun, T.6
Shen, J.7
Chen, K.8
Jiang, H.9
Shen, X.10
-
110
-
-
20744453676
-
Critical assessment of important regions in the subunit association and catalytic action of the severe acute respiratory syndrome coronavirus main protease
-
Hsu, W.-C.; Chang, H.-C.; Chou, C.-Y.; Tsai, P.-J.; Lin, P.-I.; Chang, G.-G. Critical assessment of important regions in the subunit association and catalytic action of the severe acute respiratory syndrome coronavirus main protease. J. Biol. Chem., 2005, 280, 22741-22748.
-
(2005)
J. Biol. Chem.
, vol.280
, pp. 22741-22748
-
-
Hsu, W.-C.1
Chang, H.-C.2
Chou, C.-Y.3
Tsai, P.-J.4
Lin, P.-I.5
Chang, G.-G.6
-
111
-
-
26444498493
-
Design of wide-spectrum inhibitors targeting coronavirus main proteases
-
Yang, H.; Xie, W.; Xue, X.; Yang, K.; Ma, J.; Liang, W.; Zhao, Q.; Zhou, Z.; Pei, D.; Ziebuhr, J.; Hilgenfeld, R.; Yuen, K.Y.; Wong, L.; Gao, G.; Chen, S.; Chen, Z.; Ma, D.; Bartlam, M.; Rao, Z. Design of wide-spectrum inhibitors targeting coronavirus main proteases. PLoS Biol., 2005, 3, e324.
-
(2005)
PLoS Biol.
, vol.3
-
-
Yang, H.1
Xie, W.2
Xue, X.3
Yang, K.4
Ma, J.5
Liang, W.6
Zhao, Q.7
Zhou, Z.8
Pei, D.9
Ziebuhr, J.10
Hilgenfeld, R.11
Yuen, K.Y.12
Wong, L.13
Gao, G.14
Chen, S.15
Chen, Z.16
Ma, D.17
Bartlam, M.18
Rao, Z.19
-
112
-
-
9144268403
-
Biosynthesis, Purification, and Substrate Specificity of Severe Acute Respiratory Syndrome Coronavirus 3C-like Proteinase
-
DOI 10.1074/jbc.M310875200
-
Fan, K.; Wei, P.; Feng, Q.; Chen, S.; Huang, C.; Ma, L.; Lai, B.; Pei, J.; Liu, Y.; Chen, J.; Lai, L. Biosynthesis, purification, and substrate specificity of severe acute respiratory syndrome coronavirus 3C-like proteinase. J. Biol. Chem., 2004, 279, 1637-1642. (Pubitemid 38084429)
-
(2004)
Journal of Biological Chemistry
, vol.279
, Issue.3
, pp. 1637-1642
-
-
Fan, K.1
Wei, P.2
Feng, Q.3
Chen, S.4
Huang, C.5
Ma, L.6
Lai, B.7
Pei, J.8
Liu, Y.9
Chen, J.10
Lai, L.11
-
113
-
-
34547627163
-
Substrate specificity profiling and identification of a new class of inhibitor for the major protease of the SARS coronavirus
-
Goetz, D.H.; Choe, Y.; Hansell, E.; Chen, Y.T.; McDowell, M.; Jonsson, C.B.; Roush, W.R.; McKerrow, J.; Craik, C.S. Substrate specificity profiling and identification of a new class of inhibitor for the major protease of the SARS coronavirus. Biochemistry, 2007, 46, 8744-8752.
-
(2007)
Biochemistry
, vol.46
, pp. 8744-8752
-
-
Goetz, D.H.1
Choe, Y.2
Hansell, E.3
Chen, Y.T.4
McDowell, M.5
Jonsson, C.B.6
Roush, W.R.7
McKerrow, J.8
Craik, C.S.9
-
114
-
-
2942750460
-
Virtual screening for SARS-CoV protease based on KZ7088 pharmacophore points
-
Sirois, S.; Wei, D.Q.; Du, Q.; Chou, K.C. Virtual screening for SARS-CoV protease based on KZ7088 pharmacophore points. J. Chem. Inf. Comput. Sci., 2004, 44, 1111-1122.
-
(2004)
J. Chem. Inf. Comput. Sci.
, vol.44
, pp. 1111-1122
-
-
Sirois, S.1
Wei, D.Q.2
Du, Q.3
Chou, K.C.4
-
115
-
-
33846623636
-
pro with Enhanced Activity: Application as a Novel Tag-cleavage Endopeptidase for Protein Overproduction
-
DOI 10.1016/j.jmb.2006.11.073, PII S0022283606016329
-
Xue, X.; Yang, H.; Shen, W.; Zhao, Q.; Li, J.; Yang, K.; Chen, C.; Jin, Y.; Bartlam, M.; Rao, Z. Production of authentic SARS-CoV M(pro) with enhanced activity: application as a novel tag-cleavage endopeptidase for protein overproduction. J. Mol. Biol., 2007, 366,965-975. (Pubitemid 46175874)
-
(2007)
Journal of Molecular Biology
, vol.366
, Issue.3
, pp. 965-975
-
-
Xue, X.1
Yang, H.2
Shen, W.3
Zhao, Q.4
Li, J.5
Yang, K.6
Chen, C.7
Jin, Y.8
Bartlam, M.9
Rao, Z.10
-
116
-
-
0033535596
-
Structure-based design, synthesis, and biological evaluation of irreversible human rhinovirus 3C protease inhibitors. 4. Incorporation of P1 lactam moieties as L-glutamine replacements
-
Dragovich, P.S.; Prins, T.J.; Zhou, R.; Webber, S.E.; Marakovits, J.T.; Fuhrman, S.A.; Patick, A.K.; Matthews, D.A.; Lee, C.A.; Ford, C.E.; Burke, B.J.; Rejto, P.A.; Hendrickson, T.F.; Tuntland, T.; Brown, E.L.; Meador, J.W., 3rd; Ferre, R.A.; Harr, J.E.; Kosa, M.B.; Worland, S.T. Structure-based design, synthesis, and biological evaluation of irreversible human rhinovirus 3C protease inhibitors. 4. Incorporation of P1 lactam moieties as L-glutamine replacements. J. Med. Chem., 1999, 42, 1213-1224.
-
(1999)
J. Med. Chem.
, vol.42
, pp. 1213-1224
-
-
Dragovich, P.S.1
Prins, T.J.2
Zhou, R.3
Webber, S.E.4
Marakovits, J.T.5
Fuhrman, S.A.6
Patick, A.K.7
Matthews, D.A.8
Lee, C.A.9
Ford, C.E.10
Burke, B.J.11
Rejto, P.A.12
Hendrickson, T.F.13
Tuntland, T.14
Brown, E.L.15
Meador III, J.W.16
Ferre, R.A.17
Harr, J.E.18
Kosa, M.B.19
Worland, S.T.20
more..
-
117
-
-
13044300859
-
Structure-assisted design of mechanism-based irreversible inhibitors of human rhinovirus 3C protease with potent antiviral activity against multiple rhinovirus serotypes
-
Matthews, D.A.; Dragovich, P.S.; Webber, S.E.; Fuhrman, S.A.; Patick, A.K.; Zalman, L.S.; Hendrickson, T.F.; Love, R.A.; Prins, T.J.; Marakovits, J.T.; Zhou, R.; Tikhe, J.; Ford, C.E.; Meador, J.W.; Ferre, R.A.; Brown, E.L.; Binford, S.L.; Brothers, M.A.; Delisle, D.M.; Worland, S.T. Structure-assisted design of mechanism-based irreversible inhibitors of human rhinovirus 3C protease with potent antiviral activity against multiple rhinovirus serotypes. Proc. Natl. Acad. Sci. USA, 1999, 96, 11000-11007.
-
(1999)
Proc. Natl. Acad. Sci. USA
, vol.96
, pp. 11000-11007
-
-
Matthews, D.A.1
Dragovich, P.S.2
Webber, S.E.3
Fuhrman, S.A.4
Patick, A.K.5
Zalman, L.S.6
Hendrickson, T.F.7
Love, R.A.8
Prins, T.J.9
Marakovits, J.T.10
Zhou, R.11
Tikhe, J.12
Ford, C.E.13
Meador, J.W.14
Ferre, R.A.15
Brown, E.L.16
Binford, S.L.17
Brothers, M.A.18
Delisle, D.M.19
Worland, S.T.20
more..
-
118
-
-
0032870120
-
In vitro antiviral activity of AG7088, a potent inhibitor of human rhinovirus 3C protease
-
Patick, A.K.; Binford, S.L.; Brothers, M.A.; Jackson, R.L.; Ford, C.E.; Diem, M.D.; Maldonado, F.; Dragovich, P.S.; Zhou, R.; Prins, T.J.; Fuhrman, S.A.; Meador, J.W.; Zalman, L.S.; Matthews, D.A.; Worland, S.T. In vitro antiviral activity of AG7088, a potent inhibitor of human rhinovirus 3C protease. Antimicrob. Agents Chemother., 1999, 43, 2444-2450.
-
(1999)
Antimicrob. Agents Chemother.
, vol.43
, pp. 2444-2450
-
-
Patick, A.K.1
Binford, S.L.2
Brothers, M.A.3
Jackson, R.L.4
Ford, C.E.5
Diem, M.D.6
Maldonado, F.7
Dragovich, P.S.8
Zhou, R.9
Prins, T.J.10
Fuhrman, S.A.11
Meador, J.W.12
Zalman, L.S.13
Matthews, D.A.14
Worland, S.T.15
-
119
-
-
27444437908
-
Design and synthesis of peptidomimetic severe acute respiratory syndrome chymotrypsin-like protease inhibitors
-
DOI 10.1021/jm050548m
-
Ghosh, A.K.; Xi, K.; Ratia, K.; Santarsiero, B.D.; Fu, W.; Harcourt, B.H.; Rota, P.A.; Baker, S.C.; Johnson, M.E.; Mesecar, A.D. Design and synthesis of peptidomimetic severe acute respiratory syndrome chymotrypsin-like protease inhibitors. J. Med. Chem., 2005, 48, 6767-6771. (Pubitemid 41533095)
-
(2005)
Journal of Medicinal Chemistry
, vol.48
, Issue.22
, pp. 6767-6771
-
-
Ghosh, A.K.1
Xi, K.2
Ratia, K.3
Santarsiero, B.D.4
Fu, W.5
Harcourt, B.H.6
Rota, P.A.7
Baker, S.C.8
Johnson, M.E.9
Mesecar, A.D.10
-
120
-
-
22844437876
-
Inhibition of the severe acute respiratory syndrome 3CL protease by peptidomimetic alpha,beta-unsaturated esters
-
DOI 10.1016/j.bmc.2005.05.065, PII S0968089605004876
-
Shie, J.-J.; Fang, J.-M.; Kuo, T.-H.; Kuo, C.-J.; Liang, P.-H.; Huang, H.-J.; Wu, Y.-T.; Jan, J.-T.; Cheng, Y.-S.E.; Wong, C.-H. Inhibition of the severe acute respiratory syndrome 3CL protease by peptidomimetic alpha,beta -unsaturated esters. Bioorg. Med. Chem., 2005, 13, 5240-5252. (Pubitemid 41039985)
-
(2005)
Bioorganic and Medicinal Chemistry
, vol.13
, Issue.17
, pp. 5240-5252
-
-
Shie, J.-J.1
Fang, J.-M.2
Kuo, T.-H.3
Kuo, C.-J.4
Liang, P.-H.5
Huang, H.-J.6
Wu, Y.-T.7
Jan, J.-T.8
Cheng, Y.-S.E.9
Wong, C.-H.10
-
121
-
-
3142594446
-
Small molecules targeting severe acute respiratory syndrome human coronavirus
-
DOI 10.1073/pnas.0403596101
-
Wu, C.-Y.; Jan, J.-T.; Ma, S.-H.; Kuo, C.-J.; Juan, H.-F.; Cheng, Y.-S.E.; Hsu, H.-H.; Huang, H.-C.; Wu, D.; Brik, A.; Liang, F.-S.; Liu, R.-S.; Fang, J.-M.; Chen, S.-T.; Liang, P.-H.; Wong, C.-H. Small molecules targeting severe acute respiratory syndrome human coronavirus. Proc. Natl. Acad. Sci. USA, 2004, 101, 10012-10017. (Pubitemid 38898719)
-
(2004)
Proceedings of the National Academy of Sciences of the United States of America
, vol.101
, Issue.27
, pp. 10012-10017
-
-
Wu, C.-Y.1
Jan, J.-T.2
Ma, S.-H.3
Kuo, C.-J.4
Juan, H.-F.5
Cheng, Y.-S.E.6
Hsu, H.-H.7
Huang, H.-C.8
Wu, D.9
Brik, A.10
Liang, F.-S.11
Liu, R.-S.12
Fang, J.-M.13
Chen, S.-T.14
Liang, P.-H.15
Wong, C.-H.16
-
122
-
-
3042675488
-
Inhibition of severe acute respiratory syndrome coronavirus replication by niclosamide
-
DOI 10.1128/AAC.48.7.2693-2696.2004
-
Wu, C.J.; Jan, J.T.; Chen, C.M.; Hsieh, H.P.; Hwang, D.R.; Liu, H.W.; Liu, C.Y.; Huang, H.W.; Chen, S.C.; Hong, C.F.; Lin, R.K.; Chao, Y.S.; Hsu, J.T. Inhibition of severe acute respiratory syndrome coronavirus replication by niclosamide. Antimicrob. Agents Chemother., 2004, 48, 2693-2696. (Pubitemid 38823443)
-
(2004)
Antimicrobial Agents and Chemotherapy
, vol.48
, Issue.7
, pp. 2693-2696
-
-
Wu, C.-J.1
Jan, J.-T.2
Chen, C.-M.3
Hsieh, H.-P.4
Hwang, D.-R.5
Liu, H.-W.6
Liu, C.-Y.7
Huang, H.-W.8
Chen, S.-C.9
Hong, C.-F.10
Lin, R.-K.11
Chao, Y.-S.12
Hsu, J.T.A.13
-
123
-
-
21244442337
-
Discovery of potent anilide inhibitors against the severe acute respiratory syndrome 3CL protease
-
DOI 10.1021/jm050184y
-
Shie, J.-J.; Fang, J.-M.; Kuo, C.-J.; Kuo, T.-H.; Liang, P.-H.; Huang, H.-J.; Yang, W.-B.; Lin, C.-H.; Chen, J.-L.; Wu, Y.-T.; Wong, C.-H. Discovery of potent anilide inhibitors against the severe acute respiratory syndrome 3CL protease. J. Med. Chem., 2005, 48, 4469-4473. (Pubitemid 40884948)
-
(2005)
Journal of Medicinal Chemistry
, vol.48
, Issue.13
, pp. 4469-4473
-
-
Shie, J.-J.1
Fang, J.-M.2
Kuo, C.-J.3
Kuo, T.-H.4
Liang, P.-H.5
Huang, H.-J.6
Yang, W.-B.7
Lin, C.-H.8
Chen, J.-L.9
Wu, Y.-T.10
Wong, C.-H.11
-
124
-
-
0041848237
-
Binding mechanism of coronavirus main proteinase with ligands and its implication to drug design against SARS
-
Chou, K.-C.; Wei, D.-Q.; Zhong, W.-Z. Binding mechanism of coronavirus main proteinase with ligands and its implication to drug design against SARS. Biochem. Biophys. Res. Commun., 2003, 308, 148-151.
-
(2003)
Biochem. Biophys. Res. Commun.
, vol.308
, pp. 148-151
-
-
Chou, K.-C.1
Wei, D.-Q.2
Zhong, W.-Z.3
-
125
-
-
33750554701
-
Progress in computational approach to drug development against SARS
-
Chou, K.C.; Wei, D.Q.; Du, Q.S.; Sirois, S.; Zhong, W.Z. Progress in computational approach to drug development against SARS. Curr. Med. Chem., 2006, 13, 3263-3270.
-
(2006)
Curr. Med. Chem.
, vol.13
, pp. 3263-3270
-
-
Chou, K.C.1
Wei, D.Q.2
Du, Q.S.3
Sirois, S.4
Zhong, W.Z.5
-
126
-
-
6344236941
-
Polyprotein cleavage mechanism of SARS CoV Mpro and chemical modification of the octapeptide
-
Du, Q.-S.; Wang, S.-Q.; Zhu, Y.; Wei, D.-Q.; Guo, H.; Sirois, S.; Chou, K.-C. Polyprotein cleavage mechanism of SARS CoV Mpro and chemical modification of the octapeptide. Peptides (N. Y., NY, U. S.). 2004, 25, 1857-1864.
-
(2004)
Peptides (N. Y., NY, U. S.).
, vol.25
, pp. 1857-1864
-
-
Du, Q.-S.1
Wang, S.-Q.2
Zhu, Y.3
Wei, D.-Q.4
Guo, H.5
Sirois, S.6
Chou, K.-C.7
-
127
-
-
2942532706
-
Structural variations in keto-glutamines for improved inhibition against hepatitis a virus 3C proteinase
-
Jain, R.P.; Vederas, J.C. Structural variations in keto-glutamines for improved inhibition against hepatitis A virus 3C proteinase. Bioorg. Med. Chem. Lett., 2004, 14, 3655-3658.
-
(2004)
Bioorg. Med. Chem. Lett.
, vol.14
, pp. 3655-3658
-
-
Jain, R.P.1
Vederas, J.C.2
-
128
-
-
0037123412
-
Synthesis and evaluation of keto-glutamine analogues as inhibitors of hepatitis a virus 3C proteinase
-
DOI 10.1021/jo0157831
-
Ramtohul, Y.K.; James, M.N.; Vederas, J.C. Synthesis and evaluation of keto-glutamine analogues as inhibitors of hepatitis A virus 3C proteinase. J. Org. Chem., 2002, 67, 3169-3178. (Pubitemid 34517693)
-
(2002)
Journal of Organic Chemistry
, vol.67
, Issue.10
, pp. 3169-3178
-
-
Ramtohul, Y.K.1
James, M.N.G.2
Vederas, J.C.3
-
129
-
-
9744247544
-
Synthesis and evaluation of keto-glutamine analogues as potent inhibitors of severe acute respiratory syndrome 3CLpro
-
Jain, R.P.; Pettersson, H.I.; Zhang, J.; Aull, K.D.; Fortin, P.D.; Huitema, C.; Eltis, L.D.; Parrish, J.C.; James, M.N.G.; Wishart, D.S.; Vederas, J.C. Synthesis and evaluation of keto-glutamine analogues as potent inhibitors of severe acute respiratory syndrome 3CLpro. J. Med. Chem., 2004, 47, 6113-6116.
-
(2004)
J. Med. Chem.
, vol.47
, pp. 6113-6116
-
-
Jain, R.P.1
Pettersson, H.I.2
Zhang, J.3
Aull, K.D.4
Fortin, P.D.5
Huitema, C.6
Eltis, L.D.7
Parrish, J.C.8
James, M.N.G.9
Wishart, D.S.10
Vederas, J.C.11
-
130
-
-
2142713046
-
pro
-
DOI 10.1021/bi0361766
-
Bacha, U.; Barrila, J.; Velazquez-Campoy, A.; Leavitt, S.A.; Freire, E. Identification of novel inhibitors of the SARS coronavirus main protease 3CLpro. Biochemistry, 2004, 43, 4906-4912. (Pubitemid 38544444)
-
(2004)
Biochemistry
, vol.43
, Issue.17
, pp. 4906-4912
-
-
Bacha, U.1
Barrila, J.2
Velazquez-Campoy, A.3
Leavitt, S.A.4
Freire, E.5
-
131
-
-
32344449198
-
Design and synthesis of dipeptidyl glutaminyl fluoromethyl ketones as potent severe acute respiratory syndrome coronovirus (SARS-CoV) inhibitors
-
Zhang, H.Z.; Zhang, H.; Kemnitzer, W.; Tseng, B.; Cinatl, J., Jr.; Michaelis, M.; Doerr, H.W.; Cai, S.X. Design and synthesis of dipeptidyl glutaminyl fluoromethyl ketones as potent severe acute respiratory syndrome coronovirus (SARS-CoV) inhibitors. J. Med. Chem., 2006, 49, 1198-1201.
-
(2006)
J. Med. Chem.
, vol.49
, pp. 1198-1201
-
-
Zhang, H.Z.1
Zhang, H.2
Kemnitzer, W.3
Tseng, B.4
Cinatl Jr., J.5
Michaelis, M.6
Doerr, H.W.7
Cai, S.X.8
-
132
-
-
0032474754
-
Synthesis and evaluation of peptidyl Michael acceptors that inactivate human rhinovirus 3C protease and inhibit virus replication
-
Kong, J.S.; Venkatraman, S.; Furness, K.; Nimkar, S.; Shepherd, T.A.; Wang, Q.M.; Aube, J.; Hanzlik, R.P. Synthesis and evaluation of peptidyl Michael acceptors that inactivate human rhinovirus 3C protease and inhibit virus replication. J. Med. Chem., 1998, 41, 2579-2587.
-
(1998)
J. Med. Chem.
, vol.41
, pp. 2579-2587
-
-
Kong, J.S.1
Venkatraman, S.2
Furness, K.3
Nimkar, S.4
Shepherd, T.A.5
Wang, Q.M.6
Aube, J.7
Hanzlik, R.P.8
-
133
-
-
0030922322
-
In vitro and ex vivo inhibition of hepatitis a virus 3C proteinase by a peptidyl monofluoromethyl ketone
-
Morris, T.S.; Frormann, S.; Shechosky, S.; Lowe, C.; Lall, M.S.; Gauss-Muller, V.; Purcell, R.H.; Emerson, S.U.; Vederas, J.C.; Malcolm, B.A. In vitro and ex vivo inhibition of hepatitis A virus 3C proteinase by a peptidyl monofluoromethyl ketone. Bioorg. Med. Chem., 1997, 5, 797-807.
-
(1997)
Bioorg. Med. Chem.
, vol.5
, pp. 797-807
-
-
Morris, T.S.1
Frormann, S.2
Shechosky, S.3
Lowe, C.4
Lall, M.S.5
Gauss-Muller, V.6
Purcell, R.H.7
Emerson, S.U.8
Vederas, J.C.9
Malcolm, B.A.10
-
134
-
-
0021832534
-
Fluoro ketone inhibitors of hydrolytic enzymes
-
Gelb, M.H.; Svaren, J.P.; Abeles, R.H. Fluoro ketone inhibitors of hydrolytic enzymes. Biochemistry. 1985, 24, 1813-1817.
-
(1985)
Biochemistry.
, vol.24
, pp. 1813-1817
-
-
Gelb, M.H.1
Svaren, J.P.2
Abeles, R.H.3
-
135
-
-
0027172371
-
Activated ketone based inhibitors of human renin
-
Patel, D.V.; Rielly-Gauvin, K.; Ryono, D.E.; Free, C.A.; Smith, S.A.; Petrillo, E.W., Jr. Activated ketone based inhibitors of human renin. J. Med. Chem., 1993, 36, 2431-2447.
-
(1993)
J. Med. Chem.
, vol.36
, pp. 2431-2447
-
-
Patel, D.V.1
Rielly-Gauvin, K.2
Ryono, D.E.3
Free, C.A.4
Smith, S.A.5
Petrillo Jr., E.W.6
-
136
-
-
33746304862
-
Synthesis of glutamic acid and glutamine peptides possessing a trifluoromethyl ketone group as SARS-CoV 3CL protease inhibitors
-
DOI 10.1016/j.tet.2006.06.052, PII S0040402006009720
-
Sydnes, M.O.; Hayashi, Y.; Sharma, V.K.; Hamada, T.; Bacha, U.; Barrila, J.; Freire, E.; Kiso, Y. Synthesis of glutamic acid and glutamine peptides possessing a trifluoromethyl ketone group as SARS-CoV 3CL protease inhibitors. Tetrahedron. 2006, 62, 8601-8609. (Pubitemid 44107390)
-
(2006)
Tetrahedron
, vol.62
, Issue.36
, pp. 8601-8609
-
-
Sydnes, M.O.1
Hayashi, Y.2
Sharma, V.K.3
Hamada, T.4
Bacha, U.5
Barrila, J.6
Freire, E.7
Kiso, Y.8
-
137
-
-
65349120140
-
New developments for the design, synthesis and biological evaluation of potent SARS-CoV 3CL(pro) inhibitors
-
Regnier, T.; Sarma, D.; Hidaka, K.; Bacha, U.; Freire, E.; Hayashi, Y.; Kiso, Y. New developments for the design, synthesis and biological evaluation of potent SARS-CoV 3CL(pro) inhibitors. Bioorg. Med. Chem. Lett., 2009, 19, 2722-2727.
-
(2009)
Bioorg. Med. Chem. Lett.
, vol.19
, pp. 2722-2727
-
-
Regnier, T.1
Sarma, D.2
Hidaka, K.3
Bacha, U.4
Freire, E.5
Hayashi, Y.6
Kiso, Y.7
-
138
-
-
42149094009
-
Design, synthesis, and evaluation of trifluoromethyl ketones as inhibitors of SARS-CoV 3CL protease
-
Shao, Y.M.; Yang, W.B.; Kuo, T.H.; Tsai, K.C.; Lin, C.H.; Yang, A.S.; Liang, P.H.; Wong, C.H. Design, synthesis, and evaluation of trifluoromethyl ketones as inhibitors of SARS-CoV 3CL protease. Bioorg. Med. Chem., 2008, 16, 4652-4660.
-
(2008)
Bioorg. Med. Chem.
, vol.16
, pp. 4652-4660
-
-
Shao, Y.M.1
Yang, W.B.2
Kuo, T.H.3
Tsai, K.C.4
Lin, C.H.5
Yang, A.S.6
Liang, P.H.7
Wong, C.H.8
-
139
-
-
0347358966
-
Aza-peptide epoxides: Potent and selective inhibitors of Schistosoma mansoni and pig kidney legumains (asparaginyl endopeptidases)
-
James, K.E.; Gotz, M.G.; Caffrey, C.R.; Hansell, E.; Carter, W.; Barrett, A.J.; McKerrow, J.H.; Powers, J.C. Aza-peptide epoxides: potent and selective inhibitors of Schistosoma mansoni and pig kidney legumains (asparaginyl endopeptidases). Biol. Chem., 2003, 384, 1613-1618.
-
(2003)
Biol. Chem.
, vol.384
, pp. 1613-1618
-
-
James, K.E.1
Gotz, M.G.2
Caffrey, C.R.3
Hansell, E.4
Carter, W.5
Barrett, A.J.6
McKerrow, J.H.7
Powers, J.C.8
-
140
-
-
1542328053
-
Design, Synthesis, and Evaluation of Aza-Peptide Epoxides as Selective and Potent Inhibitors of Caspases-1, -3, -6, and -8
-
DOI 10.1021/jm0305016
-
James, K.E.; Asgian, J.L.; Li, Z.Z.; Ekici, O.D.; Rubin, J.R.; Mikolajczyk, J.; Salvesen, G.S.; Powers, J.C. Design, synthesis, and evaluation of aza-peptide epoxides as selective and potent inhibitors of caspases-1, -3, -6, and -8. J. Med. Chem., 2004, 47, 1553-1574. (Pubitemid 38327479)
-
(2004)
Journal of Medicinal Chemistry
, vol.47
, Issue.6
, pp. 1553-1574
-
-
James, K.E.1
Asgian, J.L.2
Li, Z.Z.3
Ekici, O.D.4
Rubin, J.R.5
Mikolajczyk, J.6
Salvesen, G.S.7
Powers, J.C.8
-
141
-
-
27144538090
-
Crystal structures of the main peptidase from the SARS Coronavirus inhibited by a substrate-like Aza-peptide epoxide
-
Lee, T.-W.; Cherney, M.M.; Huitema, C.; Liu, J.; James, K.E.; Powers, J.C.; Eltis, L.D.; James, M.N.G. Crystal structures of the main peptidase from the SARS Coronavirus inhibited by a substrate-like Aza-peptide epoxide. J. Mol. Biol., 2005, 353, 1137-1151.
-
(2005)
J. Mol. Biol.
, vol.353
, pp. 1137-1151
-
-
Lee, T.-W.1
Cherney, M.M.2
Huitema, C.3
Liu, J.4
James, K.E.5
Powers, J.C.6
Eltis, L.D.7
James, M.N.G.8
-
142
-
-
0027510480
-
Screening for fibrinolysis inhibitory effect of synthetic thrombin inhibitors
-
Barabas, E.; Szell, E.; Bajusz, S. Screening for fibrinolysis inhibitory effect of synthetic thrombin inhibitors. Blood Coagul. Fibrinol., 1993, 4, 243-248. (Pubitemid 23103800)
-
(1993)
Blood Coagulation and Fibrinolysis
, vol.4
, Issue.2
, pp. 243-248
-
-
Barabas, E.1
Szell, E.2
Bajusz, S.3
-
143
-
-
0027221538
-
Inhibition studies of some serine and thiol proteinases by new leupeptin analogues
-
McConnell, R.M.; York, J.L.; Frizzell, D.; Ezell, C. Inhibition studies of some serine and thiol proteinases by new leupeptin analogues. J. Med. Chem., 1993, 36, 1084-1089. (Pubitemid 23143621)
-
(1993)
Journal of Medicinal Chemistry
, vol.36
, Issue.8
, pp. 1084-1089
-
-
McConnell, R.M.1
York, J.L.2
Frizzell, D.3
Ezell, C.4
-
144
-
-
0021288767
-
Aldehydic peptides inhibiting renin
-
Fehrentz, J.A.; Heitz, A.; Castro, B.; Cazaubon, C.; Nisato, D. Aldehydic peptides inhibiting renin. FEBS Lett., 1984, 167, 273-276.
-
(1984)
FEBS Lett.
, vol.167
, pp. 273-276
-
-
Fehrentz, J.A.1
Heitz, A.2
Castro, B.3
Cazaubon, C.4
Nisato, D.5
-
145
-
-
0027465626
-
Peptide aldehydes as inhibitors of HIV protease
-
DOI 10.1016/0014-5793(93)80557-B
-
Sarubbi, E.; Seneci, P.F.; Angelastro, M.R.; Peet, N.P.; Denaro, M.; Islam, K. Peptide aldehydes as inhibitors of HIV protease. FEBS Lett., 1993, 319, 253-256. (Pubitemid 23080223)
-
(1993)
FEBS Letters
, vol.319
, Issue.3
, pp. 253-256
-
-
Sarubbi, E.1
Fausto Seneci, P.2
Angelastro, M.R.3
Peet, N.P.4
Denaro, M.5
Islam, K.6
-
146
-
-
0026507126
-
A novel heterodimeric cysteine protease is required for interleukin-1 beta processing in monocytes
-
Thornberry, N.A.; Bull, H.G.; Calaycay, J.R.; Chapman, K.T.; Howard, A.D.; Kostura, M.J.; Miller, D.K.; Molineaux, S.M.; Weidner, J.R.; Aunins, J. A novel heterodimeric cysteine protease is required for interleukin-1 beta processing in monocytes. Nature. 1992, 356, 768-774.
-
(1992)
Nature.
, vol.356
, pp. 768-774
-
-
Thornberry, N.A.1
Bull, H.G.2
Calaycay, J.R.3
Chapman, K.T.4
Howard, A.D.5
Kostura, M.J.6
Miller, D.K.7
Molineaux, S.M.8
Weidner, J.R.9
Aunins, J.10
-
147
-
-
0028027195
-
Preparation and evaluation of peptidic aspartyl hemiacetals as reversible inhibitors of interleukin-1 beta converting enzyme (ICE)
-
Graybill, T.L.; Dolle, R.E.; Helaszek, C.T.; Miller, R.E.; Ator, M.A. Preparation and evaluation of peptidic aspartyl hemiacetals as reversible inhibitors of interleukin-1 beta converting enzyme (ICE). Int. J. Pept. Protein Res., 1994, 44, 173-182.
-
(1994)
Int. J. Pept. Protein Res.
, vol.44
, pp. 173-182
-
-
Graybill, T.L.1
Dolle, R.E.2
Helaszek, C.T.3
Miller, R.E.4
Ator, M.A.5
-
148
-
-
33745906224
-
pro) inhibitors
-
DOI 10.1002/cbic.200500533
-
Al-Gharabli, S.I.; Shah, S.T.A.; Weik, S.; Schmidt, M.F.; Mesters, J.R.; Kuhn, D.; Klebe, G.; Hilgenfeld, R.; Rademann, J. An efficient method for the synthesis of peptide aldehyde libraries employed in the discovery of reversible SARS coronavirus main protease (SARS-CoV Mpro) inhibitors. Chem. Bio. Chem., 2006, 7,1048-1055. (Pubitemid 44049439)
-
(2006)
ChemBioChem
, vol.7
, Issue.7
, pp. 1048-1055
-
-
Al-Gharabli, S.I.1
Ali Shah, S.T.2
Weik, S.3
Schmidt, M.F.4
Mesters, J.R.5
Kuhn, D.6
Klebe, G.7
Hilgenfeld, R.8
Rademann, J.9
-
149
-
-
13844316622
-
Virtual screening of novel noncovalent inhibitors for SARS-CoV 3C-like proteinase
-
Liu, Z.; Huang, C.; Fan, K.; Wei, P.; Chen, H.; Liu, S.; Pei, J.; Shi, L.; Li, B.; Yang, K.; Liu, Y.; Lai, L. Virtual screening of novel noncovalent inhibitors for SARS-CoV 3C-like proteinase. J. Chem. Inf. Comput. Sci., 2005, 45, 10-17.
-
(2005)
J. Chem. Inf. Comput. Sci.
, vol.45
, pp. 10-17
-
-
Liu, Z.1
Huang, C.2
Fan, K.3
Wei, P.4
Chen, H.5
Liu, S.6
Pei, J.7
Shi, L.8
Li, B.9
Yang, K.10
Liu, Y.11
Lai, L.12
-
150
-
-
21044456863
-
Cinanserin is an inhibitor of the 3C-like proteinase of severe acute respiratory syndrome coronavirus and strongly reduces virus replication in vitro
-
DOI 10.1128/JVI.79.11.7095-7103.2005
-
Chen, L.; Gui, C.; Luo, X.; Yang, Q.; Guenther, S.; Scandella, E.; Drosten, C.; Bai, D.; He, X.; Ludewig, B.; Chen, J.; Luo, H.; Yang, Y.; Yang, Y.; Zou, J.; Thiel, V.; Chen, K.; Shen, J.; Shen, X.; Jiang, H. Cinanserin is an inhibitor of the 3C-like proteinase of severe acute respiratory syndrome coronavirus and strongly reduces virus replication in vitro. J. Virol., 2005, 79, 7095-7103. (Pubitemid 40677341)
-
(2005)
Journal of Virology
, vol.79
, Issue.11
, pp. 7095-7103
-
-
Chen, L.1
Gui, C.2
Luo, X.3
Yang, Q.4
Gunther, S.5
Scandella, E.6
Drosten, C.7
Bai, D.8
He, X.9
Ludewig, B.10
Chen, J.11
Luo, H.12
Yang, Y.13
Yang, Y.14
Zou, J.15
Thiel, V.16
Chen, K.17
Shen, J.18
Shen, X.19
Jiang, H.20
more..
-
151
-
-
0036136868
-
Consensus scoring for ligand/protein interactions
-
Clark, R.D.; Strizhev, A.; Leonard, J.M.; Blake, J.F.; Matthew, J.B. Consensus scoring for ligand/protein interactions. J. Mol. Graph. Model., 2002, 20, 281-295.
-
(2002)
J. Mol. Graph. Model.
, vol.20
, pp. 281-295
-
-
Clark, R.D.1
Strizhev, A.2
Leonard, J.M.3
Blake, J.F.4
Matthew, J.B.5
-
152
-
-
33747458480
-
Structure-based drug design and structural biology study of novel nonpeptide inhibitors of severe acute respiratory syndrome coronavirus main protease
-
Lu, I.L.; Mahindroo, N.; Liang, P.-H.; Peng, Y.-H.; Kuo, C.-J.; Tsai, K.-C.; Hsieh, H.-P.; Chao, Y.-S.; Wu, S.-Y. Structure-based drug design and structural biology study of novel nonpeptide inhibitors of severe acute respiratory syndrome coronavirus main protease. J. Med. Chem., 2006, 49, 5154-5161.
-
(2006)
J. Med. Chem.
, vol.49
, pp. 5154-5161
-
-
Lu, I.L.1
Mahindroo, N.2
Liang, P.-H.3
Peng, Y.-H.4
Kuo, C.-J.5
Tsai, K.-C.6
Hsieh, H.-P.7
Chao, Y.-S.8
Wu, S.-Y.9
-
153
-
-
30344480804
-
From genome to drug lead: Identification of a small-molecule inhibitor of the SARS virus
-
Dooley, A.J.; Shindo, N.; Taggart, B.; Park, J.-G.; Pang, Y.-P. From genome to drug lead: Identification of a small-molecule inhibitor of the SARS virus. Bioorg. Med. Chem. Lett., 2006, 16, 830-833.
-
(2006)
Bioorg. Med. Chem. Lett.
, vol.16
, pp. 830-833
-
-
Dooley, A.J.1
Shindo, N.2
Taggart, B.3
Park, J.-G.4
Pang, Y.-P.5
-
154
-
-
33745133367
-
Discovery of a novel family of SARS-CoV protease inhibitors by virtual screening and 3D-QSAR studies
-
Tsai, K.C.; Chen, S.Y.; Liang, P.H.; Lu, I.L.; Mahindroo, N.; Hsieh, H.P.; Chao, Y.S.; Liu, L.; Liu, D.; Lien, W.; Lin, T.H.; Wu, S.Y. Discovery of a novel family of SARS-CoV protease inhibitors by virtual screening and 3D-QSAR studies. J. Med. Chem., 2006, 49, 3485-3495.
-
(2006)
J. Med. Chem.
, vol.49
, pp. 3485-3495
-
-
Tsai, K.C.1
Chen, S.Y.2
Liang, P.H.3
Lu, I.L.4
Mahindroo, N.5
Hsieh, H.P.6
Chao, Y.S.7
Liu, L.8
Liu, D.9
Lien, W.10
Lin, T.H.11
Wu, S.Y.12
-
155
-
-
33751551251
-
Drug design targeting the main protease, the achilles' heel of coronaviruses
-
Yang, H.; Bartlam, M.; Rao, Z. Drug design targeting the main protease, the achilles' heel of coronaviruses. Curr. Pharm. Des., 2006, 12, 4573-4590.
-
(2006)
Curr. Pharm. Des.
, vol.12
, pp. 4573-4590
-
-
Yang, H.1
Bartlam, M.2
Rao, Z.3
-
156
-
-
4644343545
-
Identification of novel smallmolecule inhibitors of severe acute respiratory syndromeassociated Coronavirus by chemical genetics
-
Kao, R.Y.; Tsui, W.H.W.; Lee, T.S.W.; Tanner, J.A.; Watt, R.M.; Huang, J.-D.; Hu, L.; Chen, G.; Chen, Z.; Zhang, L.; He, T.; Chan, K.-H.; Tse, H.; To, A.P.C.; Ng, L.W.Y.; Wong, B.C.W.; Tsoi, H.-W.; Yang, D.; Ho, D.D.; Yuen, K.-Y. Identification of novel smallmolecule inhibitors of severe acute respiratory syndromeassociated Coronavirus by chemical genetics. Chem. Biol., 2004, 11, 1293-1299.
-
(2004)
Chem. Biol.
, vol.11
, pp. 1293-1299
-
-
Kao, R.Y.1
Tsui, W.H.W.2
Lee, T.S.W.3
Tanner, J.A.4
Watt, R.M.5
Huang, J.-D.6
Hu, L.7
Chen, G.8
Chen, Z.9
Zhang, L.10
He, T.11
Chan, K.-H.12
Tse, H.13
To, A.P.C.14
Ng, L.W.Y.15
Wong, B.C.W.16
Tsoi, H.-W.17
Yang, D.18
Ho, D.D.19
Yuen, K.-Y.20
more..
-
157
-
-
5544272766
-
High-throughput screening identifies inhibitors of the SARS coronavirus main proteinase
-
DOI 10.1016/j.chembiol.2004.08.011, PII S1074552104002443
-
Blanchard, J.E.; Elowe, N.H.; Huitema, C.; Fortin, P.D.; Cechetto, J.D.; Eltis, L.D.; Brown, E.D. High-throughput screening identifies inhibitors of the SARS coronavirus main proteinase. Chem. Biol., 2004, 11, 1445-1453. (Pubitemid 39365165)
-
(2004)
Chemistry and Biology
, vol.11
, Issue.10
, pp. 1445-1453
-
-
Blanchard, J.E.1
Elowe, N.H.2
Huitema, C.3
Fortin, P.D.4
Cechetto, J.D.5
Eltis, L.D.6
Brown, E.D.7
-
158
-
-
58649118410
-
Individual and common inhibitors of coronavirus and picornavirus main proteases
-
Kuo, C.J.; Liu, H.G.; Lo, Y.K.; Seong, C.M.; Lee, K.I.; Jung, Y.S.; Liang, P.H. Individual and common inhibitors of coronavirus and picornavirus main proteases. FEBS Lett., 2009, 583, 549-555.
-
(2009)
FEBS Lett.
, vol.583
, pp. 549-555
-
-
Kuo, C.J.1
Liu, H.G.2
Lo, Y.K.3
Seong, C.M.4
Lee, K.I.5
Jung, Y.S.6
Liang, P.H.7
-
159
-
-
4444368730
-
Evaluation of metal-conjugated compounds as inhibitors of 3CL protease of SARS-CoV
-
Hsu, J.T.A.; Kuo, C.-J.; Hsieh, H.-P.; Wang, Y.-C.; Huang, K.-K.; Lin, C.P.C.; Huang, P.-F.; Chen, X.; Liang, P.-H. Evaluation of metal-conjugated compounds as inhibitors of 3CL protease of SARS-CoV. FEBS Lett., 2004, 574, 116-120.
-
(2004)
FEBS Lett.
, vol.574
, pp. 116-120
-
-
Hsu, J.T.A.1
Kuo, C.-J.2
Hsieh, H.-P.3
Wang, Y.-C.4
Huang, K.-K.5
Lin, C.P.C.6
Huang, P.-F.7
Chen, X.8
Liang, P.-H.9
-
160
-
-
20444433493
-
Screening of drugs by FRET analysis identifies inhibitors of SARS-CoV 3CL protease
-
Liu, Y.-C.; Huang, V.; Chao, T.-C.; Hsiao, C.-D.; Lin, A.; Chang, M.-F.; Chow, L.-P. Screening of drugs by FRET analysis identifies inhibitors of SARS-CoV 3CL protease. Biochem. Biophys. Res. Commun., 2005, 333, 194-199.
-
(2005)
Biochem. Biophys. Res. Commun.
, vol.333
, pp. 194-199
-
-
Liu, Y.-C.1
Huang, V.2
Chao, T.-C.3
Hsiao, C.-D.4
Lin, A.5
Chang, M.-F.6
Chow, L.-P.7
-
161
-
-
24344464802
-
Inhibition of SARS-CoV 3C-like Protease Activity by Theaflavin-3,3'- digallate (TF3)
-
Chen, C.N.; Lin, C.P.; Huang, K.K.; Chen, W.C.; Hsieh, H.P.; Liang, P.H.; Hsu, J.T. Inhibition of SARS-CoV 3C-like Protease Activity by Theaflavin-3,3'-digallate (TF3). Evid Based Compl. Alt. Med., 2005, 2, 209-215.
-
(2005)
Evid Based Compl. Alt. Med.
, vol.2
, pp. 209-215
-
-
Chen, C.N.1
Lin, C.P.2
Huang, K.K.3
Chen, W.C.4
Hsieh, H.P.5
Liang, P.H.6
Hsu, J.T.7
-
162
-
-
27444440007
-
A new lead for nonpeptidic active-site-directed inhibitors of the severe acute respiratory syndrome coronavirus main protease discovered by a combination of screening and docking methods
-
DOI 10.1021/jm0501782
-
Kaeppler, U.; Stiefl, N.; Schiller, M.; Vicik, R.; Breuning, A.; Schmitz, W.; Rupprecht, D.; Schmuck, C.; Baumann, K.; Ziebuhr, J.; Schirmeister, T. A new lead for nonpeptidic active-site-directed inhibitors of the severe acute respiratory syndrome coronavirus main protease discovered by a combination of screening and docking methods. J. Med. Chem., 2005, 48, 6832-6842. (Pubitemid 41533105)
-
(2005)
Journal of Medicinal Chemistry
, vol.48
, Issue.22
, pp. 6832-6842
-
-
Kaeppler, U.1
Stiefl, N.2
Schiller, M.3
Vicik, R.4
Breuning, A.5
Schmitz, W.6
Rupprecht, D.7
Schmuck, C.8
Baumann, K.9
Ziebuhr, J.10
Schirmeister, T.11
-
163
-
-
25144432483
-
Anti-SARS coronavirus 3C-like protease effects of Isatis indigotica root and plant-derived phenolic compounds
-
Lin, C.-W.; Tsai, F.-J.; Tsai, C.-H.; Lai, C.-C.; Wan, L.; Ho, T.-Y.; Hsieh, C.-C.; Chao, P.-D.L. Anti-SARS coronavirus 3C-like protease effects of Isatis indigotica root and plant-derived phenolic compounds. Antiviral Res., 2005, 68, 36-42.
-
(2005)
Antiviral Res.
, vol.68
, pp. 36-42
-
-
Lin, C.-W.1
Tsai, F.-J.2
Tsai, C.-H.3
Lai, C.-C.4
Wan, L.5
Ho, T.-Y.6
Hsieh, C.-C.7
Chao, P.-D.L.8
-
164
-
-
0242348704
-
Identifying inhibitors of the SARS coronavirus proteinase
-
DOI 10.1016/j.bmcl.2003.08.066
-
Jenwitheesuk, E.; Samudrala, R. Identifying inhibitors of the SARS coronavirus proteinase. Bioorg. Med. Chem. Lett., 2003, 13, 3989-3992. (Pubitemid 37338433)
-
(2003)
Bioorganic and Medicinal Chemistry Letters
, vol.13
, Issue.22
, pp. 3989-3992
-
-
Jenwitheesuk, E.1
Samudrala, R.2
-
165
-
-
34247499804
-
In silico prediction of SARS protease inhibitors by virtual high throughput screening
-
DOI 10.1111/j.1747-0285.2007.00475.x
-
Plewczynski, D.; Hoffmann, M.; von Grotthuss, M.; Ginalski, K.; Rychewski, L. In silico prediction of SARS protease inhibitors by virtual high throughput screening. Chem. Biol. Drug Des., 2007, 69, 269-279. (Pubitemid 46663179)
-
(2007)
Chemical Biology and Drug Design
, vol.69
, Issue.4
, pp. 269-279
-
-
Plewczynski, D.1
Hoffmann, M.2
Von Grotthuss, M.3
Ginalski, K.4
Rychewski, L.5
-
166
-
-
2142657824
-
Old drugs as lead compounds for a new disease? Binding analysis of SARS coronavirus main proteinase with HIV, psychotic and parasite drugs
-
Zhang, X.W.; Yap, Y.L. Old drugs as lead compounds for a new disease? Binding analysis of SARS coronavirus main proteinase with HIV, psychotic and parasite drugs. Bioorg. Med. Chem., 2004, 12, 2517-2521.
-
(2004)
Bioorg. Med. Chem.
, vol.12
, pp. 2517-2521
-
-
Zhang, X.W.1
Yap, Y.L.2
-
167
-
-
26444578169
-
Expanding the frontiers of existing antiviral drugs: Possible effects of HIV-1 protease inhibitors against SARS and avian influenza
-
DOI 10.1016/j.jcv.2005.03.005, PII S1386653205000880
-
Savarino, A. Expanding the frontiers of existing antiviral drugs: possible effects of HIV-1 protease inhibitors against SARS and avian influenza. J. Clin. Virol., 2005, 34, 170-178. (Pubitemid 41427312)
-
(2005)
Journal of Clinical Virology
, vol.34
, Issue.3
, pp. 170-178
-
-
Savarino, A.1
-
168
-
-
11844290106
-
Generation of predictive pharmacophore model for SARS-coronavirus main proteinase
-
Zhang, X.W.; Yap, Y.L.; Altmeyer, R.M. Generation of predictive pharmacophore model for SARS-coronavirus main proteinase. Eur. J. Med. Chem., 2005, 40, 57-62.
-
(2005)
Eur. J. Med. Chem.
, vol.40
, pp. 57-62
-
-
Zhang, X.W.1
Yap, Y.L.2
Altmeyer, R.M.3
-
169
-
-
44949155667
-
Sensitized detection of inhibitory fragments and iterative development of non-peptidic protease inhibitors by dynamic ligation screening
-
Schmidt, M.F.; Isidro-Llobet, A.; Lisurek, M.; El-Dahshan, A.; Tan, J.; Hilgenfeld, R.; Rademann, J. Sensitized detection of inhibitory fragments and iterative development of non-peptidic protease inhibitors by dynamic ligation screening. Angew. Chem. Int. Ed. Engl., 2008, 47, 3275-3278.
-
(2008)
Angew. Chem. Int. Ed. Engl.
, vol.47
, pp. 3275-3278
-
-
Schmidt, M.F.1
Isidro-Llobet, A.2
Lisurek, M.3
El-Dahshan, A.4
Tan, J.5
Hilgenfeld, R.6
Rademann, J.7
-
170
-
-
57749099137
-
Evidence of artemisinin-resistant malaria in western Cambodia
-
Noedl, H.; Se, Y.; Schaecher, K.; Smith, B.L.; Socheat, D.; Fukuda, M.M. Evidence of artemisinin-resistant malaria in western Cambodia. N. Engl. J. Med., 2008, 359, 2619-2620.
-
(2008)
N. Engl. J. Med.
, vol.359
, pp. 2619-2620
-
-
Noedl, H.1
Se, Y.2
Schaecher, K.3
Smith, B.L.4
Socheat, D.5
Fukuda, M.M.6
|