-
3
-
-
0032812781
-
Cysteine proteinase inhibitors kill cultured bloodstream forms of
-
1:CAS:528:DyaK1MXhvF2jurk%3D
-
L. Troeberg R.E. Morty R.N. Pike et al. Cysteine proteinase inhibitors kill cultured bloodstream forms of Trypanosoma brucei brucei Exp. Parsitol. 1999 91 349 355 10.1006/expr.1998.4386 1:CAS:528:DyaK1MXhvF2jurk%3D
-
(1999)
Trypanosoma brucei brucei Exp. Parsitol
, vol.91
, pp. 349-355
-
-
Troeberg, L.1
Morty, R.E.2
Pike, R.N.3
-
4
-
-
0025040524
-
Lysis of trypanosomes by peptidyl fluoromethyl ketones
-
F. Ashall H. Angliker E. Shaw Lysis of trypanosomes by peptidyl fluoromethyl ketones Biochim. Biophys. Res. Comm. 1990 70 923 929 10.1016/0006-291X(90)92179-4
-
(1990)
Biochim. Biophys. Res. Comm
, vol.70
, pp. 923-929
-
-
Ashall, F.1
Angliker, H.2
Shaw, E.3
-
5
-
-
0032541311
-
Cysteine proteinase inhibitors cure an experimental Trypanosoma cruzi infection
-
1:CAS:528:DyaK1cXlsFClsbw%3D, 9705954, 2213346
-
J.C. Engel P.S. Doyle I. Hsieh J.H. McKerrow Cysteine proteinase inhibitors cure an experimental Trypanosoma cruzi infection J. Exp. Med. 1998 188 725 734 10.1084/jem.188.4.725 1:CAS:528:DyaK1cXlsFClsbw%3D 9705954 2213346
-
(1998)
J. Exp. Med
, vol.188
, pp. 725-734
-
-
Engel, J.C.1
Doyle, P.S.2
Hsieh, I.3
McKerrow, J.H.4
-
6
-
-
0026541179
-
Characterisation of a cysteine protease from bloodstream forms of
-
1:CAS:528:DyaK38XisFSrsb0%3D, 1740149
-
Z.R. Mbawa I.D. Gumm E. Shaw J.D. Lonsdale-Eccles Characterisation of a cysteine protease from bloodstream forms of Trypanosoma congolense. Eur. J. Biochem. 1992 204 371 379 10.1111/j.1432-1033.1992.tb16646.x 1:CAS:528:DyaK38XisFSrsb0%3D 1740149
-
(1992)
Trypanosoma congolense. Eur. J. Biochem
, vol.204
, pp. 371-379
-
-
Mbawa, Z.R.1
Gumm, I.D.2
Shaw, E.3
Lonsdale-Eccles, J.D.4
-
7
-
-
0030607410
-
Cysteine protease inhibitors block schistosome hemoglobin degradation in vitro and decrease worm burden and egg production
-
1:CAS:528:DyaK28XlvVeisrw%3D, 8898333
-
M.M. Wasilewski K.C. Lim J. Phillips J.H. McKerrow Cysteine protease inhibitors block schistosome hemoglobin degradation in vitro and decrease worm burden and egg production in vivo. Mol. Biochem. Parasitol. 1996 81 179 189 10.1016/0166-6851(96)02703-X 1:CAS:528:DyaK28XlvVeisrw%3D 8898333
-
(1996)
in vivo. Mol. Biochem. Parasitol
, vol.81
, pp. 179-189
-
-
Wasilewski, M.M.1
Lim, K.C.2
Phillips, J.3
McKerrow, J.H.4
-
8
-
-
0027512171
-
Inhibition of a Plasmodium vinckei cysteine proteinase cures murine malaria
-
1:CAS:528:DyaK3sXksVSgs7w%3D, 8450035, 288059
-
P.J. Rosenthal G.K. Lee R.E. Smith Inhibition of a Plasmodium vinckei cysteine proteinase cures murine malaria J. Clin. Invest. 1993 91 1052 1056 10.1172/JCI116262 1:CAS:528:DyaK3sXksVSgs7w%3D 8450035 288059
-
(1993)
J. Clin. Invest
, vol.91
, pp. 1052-1056
-
-
Rosenthal, P.J.1
Lee, G.K.2
Smith, R.E.3
-
9
-
-
0025093614
-
Inhibition of intraerythrocytic development of Plasmodium falciparum by proteinase inhibitors
-
1:CAS:528:DyaK3cXhtlWqsL8%3D, 2403526
-
K.A. Rockett J.H.L. Playfair F. Ashall G.A.T. Targett H. Angliker E. Shaw Inhibition of intraerythrocytic development of Plasmodium falciparum by proteinase inhibitors FEBS Lett. 1990 259 257 259 10.1016/0014-5793(90)80022-B 1:CAS:528:DyaK3cXhtlWqsL8%3D 2403526
-
(1990)
FEBS Lett
, vol.259
, pp. 257-259
-
-
Rockett, K.A.1
Playfair, J.H.L.2
Ashall, F.3
Targett, G.A.T.4
Angliker, H.5
Shaw, E.6
-
10
-
-
0031282334
-
Leishmania major molecular modeling of cysteine proteases and prediction of new non-peptide inhibitors
-
1:CAS:528:DyaK2sXns1yisLg%3D, 9371086
-
P.M. Selzer X. Chen V.J. Chan et al. Leishmania major molecular modeling of cysteine proteases and prediction of new non-peptide inhibitors Exp. Parasitol. 1997 87 212 221 10.1006/expr.1997.4220 1:CAS:528:DyaK2sXns1yisLg%3D 9371086
-
(1997)
Exp. Parasitol
, vol.87
, pp. 212-221
-
-
Selzer, P.M.1
Chen, X.2
Chan, V.J.3
-
11
-
-
0027398184
-
Peptide-fluoromethyl ketones arrest intracellular replication and intercellular transmission of
-
1:CAS:528:DyaK3sXit1Cqu7o%3D, 8459830
-
G. Harth N. Andrews A.A. Mills J.C. Engel R. Smith J.H. McKerrow Peptide-fluoromethyl ketones arrest intracellular replication and intercellular transmission of Trypanosoma cruzi. Mol. Biochem. Parasitol. 1993 58 17 24 10.1016/0166-6851(93)90086-D 1:CAS:528:DyaK3sXit1Cqu7o%3D 8459830
-
(1993)
Trypanosoma cruzi. Mol. Biochem. Parasitol
, vol.58
, pp. 17-24
-
-
Harth, G.1
Andrews, N.2
Mills, A.A.3
Engel, J.C.4
Smith, R.5
McKerrow, J.H.6
-
12
-
-
0026606269
-
Inhibitors of the major cysteinyl proteinase (GP57/51) impair host cell invasion and arrest the intracellular development of
-
M.N.L. Mierelles L. Juliano E. Carmona et al. Inhibitors of the major cysteinyl proteinase (GP57/51) impair host cell invasion and arrest the intracellular development of Trypanosoma cruzi in vitro. Mol. Biochem. Parasitol. 1992 52 175 184 10.1016/0166-6851(92)90050-T
-
(1992)
Trypanosoma cruzi in vitro. Mol. Biochem. Parasitol
, vol.52
, pp. 175-184
-
-
Mierelles, M.N.L.1
Juliano, L.2
Carmona, E.3
-
13
-
-
0029594562
-
In vitro antimalarial activity of chalcones and their derivatives
-
1:CAS:528:DyaK2MXps1Gjtrw%3D, 8544179
-
R. Li G.L. Kenyon F.E. Cohen et al. In vitro antimalarial activity of chalcones and their derivatives J. Med. Chem. 1995 38 5031 5037 10.1021/jm00026a010 1:CAS:528:DyaK2MXps1Gjtrw%3D 8544179
-
(1995)
J. Med. Chem
, vol.38
, pp. 5031-5037
-
-
Li, R.1
Kenyon, G.L.2
Cohen, F.E.3
-
14
-
-
0032908492
-
Selective effect of 2′, 6′-dihydroxy-4′-methylchalcone isolated from Piper aduncum on Leishmania amazonensis. Antimicrob
-
1:CAS:528:DyaK1MXjtVejsLk%3D
-
E.C. Torres-Santos D.L. Moreira M.A.C. Kaplan M.N. Meirelles B. Rossi-Bergman Selective effect of 2′, 6′-dihydroxy-4′-methylchalcone isolated from Piper aduncum on Leishmania amazonensis. Antimicrob Agents Chemother. 1999 43 1234 1241 1:CAS:528:DyaK1MXjtVejsLk%3D
-
(1999)
Agents Chemother
, vol.43
, pp. 1234-1241
-
-
Torres-Santos, E.C.1
Moreira, D.L.2
Kaplan, M.A.C.3
Meirelles, M.N.4
Rossi-Bergman, B.5
-
15
-
-
0027480452
-
Structure-based inhibitor design by using protein models for the development of antiparasitic agents
-
1:CAS:528:DyaK3sXktVShu7o%3D, 8475107, 46345
-
C.S. Ring E. Sun J.H. McKerrow et al. Structure-based inhibitor design by using protein models for the development of antiparasitic agents Proc. Natl. Acad. Sci. U. S. A. 1993 90 3583 3587 10.1073/pnas.90.8.3583 1:CAS:528:DyaK3sXktVShu7o%3D 8475107 46345
-
(1993)
Proc. Natl. Acad. Sci. U. S. A
, vol.90
, pp. 3583-3587
-
-
Ring, C.S.1
Sun, E.2
McKerrow, J.H.3
-
16
-
-
0028500539
-
Anti-malarial drug development using models of enzyme structure
-
1:CAS:528:DyaK2cXmvFajs74%3D, 9383368
-
Z. Li X. Chen E. Davidson et al. Anti-malarial drug development using models of enzyme structure Chem. Biol. 1994 1 31 37 10.1016/1074-5521(94)90038-8 1:CAS:528:DyaK2cXmvFajs74%3D 9383368
-
(1994)
Chem. Biol
, vol.1
, pp. 31-37
-
-
Li, Z.1
Chen, X.2
Davidson, E.3
-
17
-
-
0026730489
-
Structure-based strategies for drug design and discovery
-
1:CAS:528:DyaK38Xls1eht7o%3D, 1509259
-
I.D. Kuntz Structure-based strategies for drug design and discovery Science 1992 257 1078 1082 10.1126/science.257.5073.1078 1:CAS:528:DyaK38Xls1eht7o%3D 1509259
-
(1992)
Science
, vol.257
, pp. 1078-1082
-
-
Kuntz, I.D.1
-
19
-
-
0028988032
-
A novel cultivation technique for long-term maintenance of bloodstream form trypanosomes in vitro
-
Hesse F, Selzer PM, Mühlstädt K, Duszenko M. A novel cultivation technique for long-term maintenance of bloodstream form trypanosomes in vitro. Mol. Biochem. Parasitol.70: 157–166.
-
Mol. Biochem. Parasitol
, vol.70
, pp. 157-166
-
-
Hesse, F.1
Selzer, P.M.2
Mühlstädt, K.3
Duszenko, M.4
-
20
-
-
0030017685
-
Proteases from Trypanosoma brucei brucei purification, characterisation and interactions with host regulatory molecules
-
1:CAS:528:DyaK28XktVaktb4%3D, 8706674
-
L. Troeberg R.N. Pike R.E. Morty R.K. Berry T.H.T. Coetzer J.D. Lonsdale-Eccles Proteases from Trypanosoma brucei brucei purification, characterisation and interactions with host regulatory molecules Eur. J. Biochem. 1996 238 728 736 10.1111/j.1432-1033.1996.0728w.x 1:CAS:528:DyaK28XktVaktb4%3D 8706674
-
(1996)
Eur. J. Biochem
, vol.238
, pp. 728-736
-
-
Troeberg, L.1
Pike, R.N.2
Morty, R.E.3
Berry, R.K.4
Coetzer, T.H.T.5
Lonsdale-Eccles, J.D.6
-
21
-
-
0026708693
-
Proteolytically active complexes of cathepsin L and a cysteine proteinase inhibitor; purification and demonstration of their formation
-
1:CAS:528:DyaK38XlsVGqsbo%3D, 1567216
-
R.N. Pike T.H.T. Coetzer C. Dennison Proteolytically active complexes of cathepsin L and a cysteine proteinase inhibitor; purification and demonstration of their formation in vitro. Arch. Biochem. Biophys. 1992 294 623 629 10.1016/0003-9861(92)90734-E 1:CAS:528:DyaK38XlsVGqsbo%3D 1567216
-
(1992)
in vitro. Arch. Biochem. Biophys
, vol.294
, pp. 623-629
-
-
Pike, R.N.1
Coetzer, T.H.T.2
Dennison, C.3
-
22
-
-
0019765848
-
Cathepsin B, cathepsin H and cathepsin L
-
A.J. Barrett H. Kirschke Cathepsin B, cathepsin H and cathepsin L Methods Enzymol 1981 80C 535 561 10.1016/S0076-6879(81)80043-2
-
(1981)
Methods Enzymol
, vol.80C
, pp. 535-561
-
-
Barrett, A.J.1
Kirschke, H.2
-
23
-
-
0019948262
-
L-trans-epoxysuccinyl-leucylamido(4-guanidino) butane (E-64) and its analogues as inhibitors of cysteine proteinases including cathepsins B, H and L
-
1:CAS:528:DyaL38XhvFGksr0%3D, 7044372, 1163625
-
A.J. Barrett A.A. Kembhavi M.A. Brown et al. L-trans-epoxysuccinyl-leucylamido(4-guanidino) butane (E-64) and its analogues as inhibitors of cysteine proteinases including cathepsins B, H and L Biochem. J. 1982 201 189 198 10.1042/bj2010189 1:CAS:528:DyaL38XhvFGksr0%3D 7044372 1163625
-
(1982)
Biochem. J
, vol.201
, pp. 189-198
-
-
Barrett, A.J.1
Kembhavi, A.A.2
Brown, M.A.3
-
24
-
-
0002006941
-
Inhibition of proteolytic enzymes, p. 83–104
-
Benyon R.J., Bond J.S., (eds), Oxford, IRL Press
-
G. Salvesen K. Nagase R.J. Benyon J.S. Bond Inhibition of proteolytic enzymes, p. 83–104 Proteolytic Enzymes: A Practical Approach 1989 Oxford IRL Press
-
(1989)
Proteolytic Enzymes: A Practical Approach
-
-
Salvesen, G.1
Nagase, K.2
-
25
-
-
0028790929
-
Mature cathepsin L is substantially active in the ionic milieu of the extracellular medium
-
1:CAS:528:DyaK2MXpvVektbk%3D, 7503566
-
F.M. Dehrmann T.H.T. Coetzer R.N. Pike C. Dennison Mature cathepsin L is substantially active in the ionic milieu of the extracellular medium Arch. Biochem. Biophys. 1995 324 93 98 10.1006/abbi.1995.9924 1:CAS:528:DyaK2MXpvVektbk%3D 7503566
-
(1995)
Arch. Biochem. Biophys
, vol.324
, pp. 93-98
-
-
Dehrmann, F.M.1
Coetzer, T.H.T.2
Pike, R.N.3
Dennison, C.4
-
26
-
-
0031024171
-
Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings
-
1:CAS:528:DyaK2sXktlKlsQ%3D%3D
-
C.A. Lipinski F. Lombardo B.W. Dominy P.J. Feeny Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings Adv. Drug Delivery Rev. 1997 23 3 25 10.1016/S0169-409X(96)00423-1 1:CAS:528:DyaK2sXktlKlsQ%3D%3D
-
(1997)
Adv. Drug Delivery Rev
, vol.23
, pp. 3-25
-
-
Lipinski, C.A.1
Lombardo, F.2
Dominy, B.W.3
Feeny, P.J.4
-
28
-
-
0029045156
-
The cysteine protease of Trypanosoma cruzi as a model for antiparasitic drug design
-
1:CAS:528:DyaK2MXnslWjsbk%3D, 15275323
-
J.H. McKerrow M.E. McGrath J.C. Engel The cysteine protease of Trypanosoma cruzi as a model for antiparasitic drug design Parasitol. Today 1995 11 279 282 10.1016/0169-4758(95)80039-5 1:CAS:528:DyaK2MXnslWjsbk%3D 15275323
-
(1995)
Parasitol. Today
, vol.11
, pp. 279-282
-
-
McKerrow, J.H.1
McGrath, M.E.2
Engel, J.C.3
-
30
-
-
0024334026
-
Plasmodium falciparum inhibitors of lysosomal cysteine proteinases inhibit a trophozoite proteinase and block parasite development
-
1:CAS:528:DyaL1MXlt12mtbg%3D, 2671722
-
P.J. Rosenthal J.H. McKerrow D. Rasnick J.H. Leech Plasmodium falciparum inhibitors of lysosomal cysteine proteinases inhibit a trophozoite proteinase and block parasite development Mol. Biochem. Parasitol. 1989 35 177 184 10.1016/0166-6851(89)90120-5 1:CAS:528:DyaL1MXlt12mtbg%3D 2671722
-
(1989)
Mol. Biochem. Parasitol
, vol.35
, pp. 177-184
-
-
Rosenthal, P.J.1
McKerrow, J.H.2
Rasnick, D.3
Leech, J.H.4
|