-
2
-
-
4344709649
-
WHO: African trypanosomiasis or sleeping sickness
-
WHO: African trypanosomiasis or sleeping sickness. World Health Org. Fact Sheet (2001) 259. http://www.who.int/mediacentre/factsheets/fs259/en/
-
(2001)
World Health Org. Fact Sheet
, vol.259
-
-
-
4
-
-
0002112085
-
Current public health status of the trypanosomiases and leishmaniases
-
Hide G, Mottram JC, Coombs GH, Holmes PH (Eds), CAB International, Wallingford, Oxon, UK
-
MOLYNEUX DH: Current public health status of the trypanosomiases and leishmaniases. In: Trypanosomiasis and Leishmaniasis: Biology and Control. Hide G, Mottram JC, Coombs GH, Holmes PH (Eds), CAB International, Wallingford, Oxon, UK (1997):39-50.
-
(1997)
Trypanosomiasis and Leishmaniasis: Biology and Control
, pp. 39-50
-
-
Molyneux, D.H.1
-
5
-
-
0142258170
-
Chemotherapy of human African trypanosomiasis: Current and future prospects
-
FAIRLAMB AH: Chemotherapy of human African trypanosomiasis: current and future prospects. Trends Parasitol. (2003) 19(11):488-494.
-
(2003)
Trends Parasitol.
, vol.19
, Issue.11
, pp. 488-494
-
-
Fairlamb, A.H.1
-
6
-
-
0142227145
-
Specific chemotherapy of Chagas disease: Controversies and advances
-
URBINA JA, DOCAMPO R: Specific chemotherapy of Chagas disease: controversies and advances. Trends Parasitol. (2003) 19(1):495-501.
-
(2003)
Trends Parasitol.
, vol.19
, Issue.1
, pp. 495-501
-
-
Urbina, J.A.1
Docampo, R.2
-
7
-
-
0036359943
-
A critical review on Chagas disease chemotherapy
-
COURA JR, DE CASTRO SL: A critical review on Chagas disease chemotherapy. Mem. Inst. Oswaldo Cruz (2002) 97(1):3-24.
-
(2002)
Mem. Inst. Oswaldo Cruz
, vol.97
, Issue.1
, pp. 3-24
-
-
Coura, J.R.1
De Castro, S.L.2
-
8
-
-
10344250495
-
Treatment and control of human African trypanosomiasis
-
JANNIN J, CATTAND P: Treatment and control of human African trypanosomiasis. Curr. Opin. Infect. Dis. (2004) 17(6):564-571.
-
(2004)
Curr. Opin. Infect. Dis.
, vol.17
, Issue.6
, pp. 564-571
-
-
Jannin, J.1
Cattand, P.2
-
9
-
-
0036734224
-
Resurrecting the resurrection drug
-
WICKWARE P: Resurrecting the resurrection drug. Nat. Med. (2002) 8(9):908-909.
-
(2002)
Nat. Med.
, vol.8
, Issue.9
, pp. 908-909
-
-
Wickware, P.1
-
10
-
-
0034278993
-
Cysteine proteinases of trypanosome parasites: Novel targets for chemotherapy
-
CAFFREY CR, SCORY S, STEVERDING D: Cysteine proteinases of trypanosome parasites: novel targets for chemotherapy. Curr. Drug Targets (2000) 1(2):155-162.
-
(2000)
Curr. Drug Targets
, vol.1
, Issue.2
, pp. 155-162
-
-
Caffrey, C.R.1
Scory, S.2
Steverding, D.3
-
11
-
-
0030055783
-
High resolution localization of cruzipain and Ssp4 in Trypanosoma cruzi by replica staining label fracture
-
NASCIMENTO AE, DE SOUZA W: High resolution localization of cruzipain and Ssp4 in Trypanosoma cruzi by replica staining label fracture. Biol. Cell (1996) 86(1):53-58.
-
(1996)
Biol. Cell
, vol.86
, Issue.1
, pp. 53-58
-
-
Nascimento, A.E.1
De Souza, W.2
-
12
-
-
0039702904
-
Protease trafficking in two primitive eukaryotes is mediated by a prodomain protein motif
-
HUETE-PÉREZ JA, ENGEL JC, BRINEN LS, MOTTRAM JC, McKERROW JH: Protease trafficking in two primitive eukaryotes is mediated by a prodomain protein motif. J. Biol. Chem. (1999) 274(23):16249-16256.
-
(1999)
J. Biol. Chem.
, vol.274
, Issue.23
, pp. 16249-16256
-
-
Huete-Pérez, J.A.1
Engel, J.C.2
Brinen, L.S.3
Mottram, J.C.4
Mckerrow, J.H.5
-
13
-
-
0023657276
-
Lysosomal and non-lysosomal peptidyl hydrolases of the bloodstream forms of Trypanosoma brucei brucei
-
LONSDALE-ECCLES JD, GRAB DJ: Lysosomal and non-lysosomal peptidyl hydrolases of the bloodstream forms of Trypanosoma brucei brucei. Eur. J. Biochem. (1987) 169(3):467-475.
-
(1987)
Eur. J. Biochem.
, vol.169
, Issue.3
, pp. 467-475
-
-
Lonsdale-Eccles, J.D.1
Grab, D.J.2
-
14
-
-
0034767886
-
Active site mapping, biochemical properties and subcellular localization of rhodesain, the major cysteine protease of Trypanosoma brucei rhodesiense
-
CAFFREY CR, HANSELL E, LUCAS KD et al.: Active site mapping, biochemical properties and subcellular localization of rhodesain, the major cysteine protease of Trypanosoma brucei rhodesiense. Mol. Biochem. Parasitol. (2001) 118(1):61-73.
-
(2001)
Mol. Biochem. Parasitol.
, vol.118
, Issue.1
, pp. 61-73
-
-
Caffrey, C.R.1
Hansell, E.2
Lucas, K.D.3
-
16
-
-
0343433408
-
Cysteine proteases and their inhibitors
-
OTTO H-H, SCHIRMEISTER T: Cysteine proteases and their inhibitors. Chem. Rev. (1997) 97(1):133-172.
-
(1997)
Chem. Rev.
, vol.97
, Issue.1
, pp. 133-172
-
-
Otto, H.-H.1
Schirmeister, T.2
-
17
-
-
0032812781
-
Cysteine proteinase inhibitors kill cultured bloodstream forms of Trypanosoma brucei brucei
-
TROEBERG L, MORTY RE, PIKE RH et al.: Cysteine proteinase inhibitors kill cultured bloodstream forms of Trypanosoma brucei brucei. Exp. Parasitol. (1999) 91(4):349-355.
-
(1999)
Exp. Parasitol.
, vol.91
, Issue.4
, pp. 349-355
-
-
Troeberg, L.1
Morty, R.E.2
Pike, R.H.3
-
19
-
-
0029099619
-
Vinyl sulfones as mechanism-based cysteine protease inhibitors
-
PALMER JT, RASNICK D, KLAUS JL, BRÖMME D: Vinyl sulfones as mechanism-based cysteine protease inhibitors. J. Med. Chem. (1995) 38(17):3193-3196.
-
(1995)
J. Med. Chem.
, vol.38
, Issue.17
, pp. 3193-3196
-
-
Palmer, J.T.1
Rasnick, D.2
Klaus, J.L.3
Brömme, D.4
-
20
-
-
0031937742
-
Cysteine protease inhibitors alter Golgi complex ultrastructure and function in Trypanosoma cruzi
-
ENGEL JC, DOYLE PS, PALMER J, HSIEH I, BAINTON DF, McKERROW JH: Cysteine protease inhibitors alter Golgi complex ultrastructure and function in Trypanosoma cruzi. J. Cell Sci. (1998) 111(5):597-606.
-
(1998)
J. Cell Sci.
, vol.111
, Issue.5
, pp. 597-606
-
-
Engel, J.C.1
Doyle, P.S.2
Palmer, J.3
Hsieh, I.4
Bainton, D.F.5
Mckerrow, J.H.6
-
21
-
-
0032541311
-
Cysteine protease inhibitors cure an experimental Trypanosoma cruzi infection
-
ENGEL JC, DOYLE PS, HSIEH I, McKERROW JH: Cysteine protease inhibitors cure an experimental Trypanosoma cruzi infection. J. Exp. Med. (1998) 188(4):725-734.
-
(1998)
J. Exp. Med.
, vol.188
, Issue.4
, pp. 725-734
-
-
Engel, J.C.1
Doyle, P.S.2
Hsieh, I.3
Mckerrow, J.H.4
-
22
-
-
0035935182
-
Potent second generation vinyl sulfonamide inhibitors of the trypanosomal cysteine protease cruzain
-
ROUSH WR, CHENG J, KNAPP-REED B et al.: Potent second generation vinyl sulfonamide inhibitors of the trypanosomal cysteine protease cruzain. Bioorg. Med. Chem. Lett. (2001) 11(20):2759-2762.
-
(2001)
Bioorg. Med. Chem. Lett.
, vol.11
, Issue.20
, pp. 2759-2762
-
-
Roush, W.R.1
Cheng, J.2
Knapp-Reed, B.3
-
23
-
-
0034252808
-
Chalcone, acyl hydrazide, and related amides kill cultured Trypanosoma brucei brucei
-
TROEBERG L, CHEN X, FLAHERTY TM et al.: Chalcone, acyl hydrazide, and related amides kill cultured Trypanosoma brucei brucei. Mol. Med. (2000) 6(8):660-669.
-
(2000)
Mol. Med.
, vol.6
, Issue.8
, pp. 660-669
-
-
Troeberg, L.1
Chen, X.2
Flaherty, T.M.3
-
24
-
-
0036199463
-
Screening of acyl hydrazide proteinase inhibitors for antiparasitic activity against Trypanosoma brucei
-
CAFFREY CR, SCHANZ M, NKEMGU-NJINKENG J et al.: Screening of acyl hydrazide proteinase inhibitors for antiparasitic activity against Trypanosoma brucei. Int. J. Antimicrob. Agents (2002) 19(3):227-231.
-
(2002)
Int. J. Antimicrob. Agents
, vol.19
, Issue.3
, pp. 227-231
-
-
Caffrey, C.R.1
Schanz, M.2
Nkemgu-Njinkeng, J.3
-
25
-
-
0033830860
-
Aryl ureas represent a new class of antitrypanosomal agents
-
DU X, HANSELL E, ENGEL JC, CAFFREY CR, COHEN FE, McKERROW JH: Aryl ureas represent a new class of antitrypanosomal agents. Chem. Biol. (2000) 7(9):733-742.
-
(2000)
Chem. Biol.
, vol.7
, Issue.9
, pp. 733-742
-
-
Du, X.1
Hansell, E.2
Engel, J.C.3
Caffrey, C.R.4
Cohen, F.E.5
Mckerrow, J.H.6
-
26
-
-
0037142343
-
Synthesis and structure-activity relationship study of potent trypanocidal thio semicarbazone inhibitors of the trypanosomal cysteine protease cruzain
-
DU X, GUO C, HANSELL E et al.: Synthesis and structure-activity relationship study of potent trypanocidal thio semicarbazone inhibitors of the trypanosomal cysteine protease cruzain. J. Med. Chem. (2002) 45(13):2695-2707.
-
(2002)
J. Med. Chem.
, vol.45
, Issue.13
, pp. 2695-2707
-
-
Du, X.1
Guo, C.2
Hansell, E.3
-
27
-
-
2542533103
-
Synthesis and structure-activity relationships of parasiticidal thiosemicarbazone cysteine protease inhibitors against Plasmodium falciparum, Trypanosoma brucei, and Trypanosoma cruzi
-
GREENBAUM DC, MACKEY Z, HANSELL E et al.: Synthesis and structure-activity relationships of parasiticidal thiosemicarbazone cysteine protease inhibitors against Plasmodium falciparum, Trypanosoma brucei, and Trypanosoma cruzi. J. Med. Chem. (2004) 47(12):3212-3219.
-
(2004)
J. Med. Chem.
, vol.47
, Issue.12
, pp. 3212-3219
-
-
Greenbaum, D.C.1
Mackey, Z.2
Hansell, E.3
-
28
-
-
0030016595
-
Structure and functions of the 20S and 26S proteasome
-
COUX O, TANAKA K, GOLDBERG AL: Structure and functions of the 20S and 26S proteasome. Ann. Rev. Biochem. (1996) 65:801-847.
-
(1996)
Ann. Rev. Biochem.
, vol.65
, pp. 801-847
-
-
Coux, O.1
Tanaka, K.2
Goldberg, A.L.3
-
29
-
-
0037013215
-
An easily dissociated 26 S proteasome catalyzes an essential ubiquitin-mediated protein degradation pathway in Trypanosoma brucei
-
LI Z, ZOU C-B, YAO Y et al.: An easily dissociated 26 S proteasome catalyzes an essential ubiquitin-mediated protein degradation pathway in Trypanosoma brucei. J. Biol. Chem. (2002) 277(18):15486-15498.
-
(2002)
J. Biol. Chem.
, vol.277
, Issue.18
, pp. 15486-15498
-
-
Li, Z.1
Zou, C.-B.2
Yao, Y.3
-
30
-
-
0343431431
-
Purification and characterization of proteasomes from Trypanosoma brucei
-
HUA S-B, TO W-Y, NGUYEN TT, WONG M-L, WANG CC: Purification and characterization of proteasomes from Trypanosoma brucei. Mol. Biochem. Parasitol. (1996) 78(1-2):33-46.
-
(1996)
Mol. Biochem. Parasitol.
, vol.78
, Issue.1-2
, pp. 33-46
-
-
Hua, S.-B.1
To, W.-Y.2
Nguyen, T.T.3
Wong, M.-L.4
Wang, C.C.5
-
31
-
-
0038521266
-
Biochemical analysis of the 20 S proteasome of Trypanosoma brucei
-
WANG CC, BOZDECH Z, LIU C-L et al.: Biochemical analysis of the 20 S proteasome of Trypanosoma brucei. J. Biol. Chem. (2003) 278(18):15800-15808.
-
(2003)
J. Biol. Chem.
, vol.278
, Issue.18
, pp. 15800-15808
-
-
Wang, C.C.1
Bozdech, Z.2
Liu, C.-L.3
-
32
-
-
0034864799
-
Proteasome inhibitors: From research tools to drug candidates
-
KISSELEV AF, GOLDBERG AL: Proteasome inhibitors: from research tools to drug candidates. Chem. Biol. (2001) 8(8):739-758.
-
(2001)
Chem. Biol.
, vol.8
, Issue.8
, pp. 739-758
-
-
Kisselev, A.F.1
Goldberg, A.L.2
-
33
-
-
0036095746
-
Antitrypanosomal activities of proteasome inhibitors
-
NKEMGU-NJINKENG J, ROSENKRANZ V, WINK M, STEVERDING D: Antitrypanosomal activities of proteasome inhibitors. Antimicrob. Agents Chemother. (2002) 46(6):2038-2040.
-
(2002)
Antimicrob. Agents Chemother.
, vol.46
, Issue.6
, pp. 2038-2040
-
-
Nkemgu-Njinkeng, J.1
Rosenkranz, V.2
Wink, M.3
Steverding, D.4
-
34
-
-
0031010398
-
Covalent modification of the active site threonine of proteasomal β subunits and the Escherichia coli homolog HsIV by a new class of inhibitors
-
BOGYO M, McMASTER JS, GACZYNSKA M, TORTORELLA D, GOLDBERG AL, PLOEGH H: Covalent modification of the active site threonine of proteasomal β subunits and the Escherichia coli homolog HsIV by a new class of inhibitors. Proc. Natl. Acad. Sci. USA (1997) 94(13):6629-6634.
-
(1997)
Proc. Natl. Acad. Sci. USA
, vol.94
, Issue.13
, pp. 6629-6634
-
-
Bogyo, M.1
Mcmaster, J.S.2
Gaczynska, M.3
Tortorella, D.4
Goldberg, A.L.5
Ploegh, H.6
-
35
-
-
0032103006
-
Substrate binding and sequence preference of the proteasome revealed by active-site-directed affinity probes
-
BOGYO M, SHIN S, McMASTER JS, PLEOGH HL: Substrate binding and sequence preference of the proteasome revealed by active-site-directed affinity probes. Chem. Biol. (1998) 5(6):307-320.
-
(1998)
Chem. Biol.
, vol.5
, Issue.6
, pp. 307-320
-
-
Bogyo, M.1
Shin, S.2
Mcmaster, J.S.3
Pleogh, H.L.4
-
36
-
-
12444256377
-
Trypanocidal activities of trileucine methyl vinyl sulfone proteasome inhibitors
-
STEVERDING D, SPACKMAN RW, ROYLE HJ, GLENN RJ: Trypanocidal activities of trileucine methyl vinyl sulfone proteasome inhibitors. Parasitol. Res. (2005) 95(1):73-76.
-
(2005)
Parasitol. Res.
, vol.95
, Issue.1
, pp. 73-76
-
-
Steverding, D.1
Spackman, R.W.2
Royle, H.J.3
Glenn, R.J.4
-
37
-
-
0034819479
-
Extended peptide-based inhibitors efficiently target the proteasome and reveal overlapping specificities of the catalytic β-subunits
-
KESSLER BM, TORTORELLA D, ALTUN M et al.: Extended peptide-based inhibitors efficiently target the proteasome and reveal overlapping specificities of the catalytic β-subunits. Chem. Biol. (2001) 8(9):913-929.
-
(2001)
Chem. Biol.
, vol.8
, Issue.9
, pp. 913-929
-
-
Kessler, B.M.1
Tortorella, D.2
Altun, M.3
-
38
-
-
4344593765
-
Trypanocidal effect of α′,β′-epoxyketones indicates that trypanosomes are particularly sensitive to inhibitors of proteasome trypsin-like activity
-
GLENN RJ, PEMBERTON AJ, ROYLE HJ et al.: Trypanocidal effect of α′,β′-epoxyketones indicates that trypanosomes are particularly sensitive to inhibitors of proteasome trypsin-like activity. Int. J. Antimicrob. Agents (2004) 24(3):286-289.
-
(2004)
Int. J. Antimicrob. Agents
, vol.24
, Issue.3
, pp. 286-289
-
-
Glenn, R.J.1
Pemberton, A.J.2
Royle, H.J.3
-
39
-
-
0343262654
-
Crystal structures of epoxomicin: 20S proteasome reveals a molecular basis for selectivity of α′,β′-epoxyketone proteasome inhibitors
-
GROLL M, KIM KB, KAIRIES N, HUBER R, CREWS CM: Crystal structures of epoxomicin:20S proteasome reveals a molecular basis for selectivity of α′,β′-epoxyketone proteasome inhibitors. J. Am. Chem. Soc. (2000) 122(6):1237-1238.
-
(2000)
J. Am. Chem. Soc.
, vol.122
, Issue.6
, pp. 1237-1238
-
-
Groll, M.1
Kim, K.B.2
Kairies, N.3
Huber, R.4
Crews, C.M.5
-
40
-
-
0034815454
-
In vitro effect of alkaloids on bloodstream forms of
-
MERSCHJOAHNN K, SPORER F, STEVERDING D, WINK M: In vitro effect of alkaloids on bloodstream forms of Trypanosoma brucei and T. congolense. Planta Med. (2001) 67(7):623-627.
-
(2001)
Trypanosoma Brucei and T. Congolense. Planta Med.
, vol.67
, Issue.7
, pp. 623-627
-
-
Merschjoahnn, K.1
Sporer, F.2
Steverding, D.3
Wink, M.4
-
41
-
-
0032539702
-
Potent and selective inhibitors of the proteasome: Dipeptidyl boronic acids
-
ADAMS J, BEHNKE M, CHEN S et al.: Potent and selective inhibitors of the proteasome: dipeptidyl boronic acids. Bioorg. Med. Chem. Lett. (1998) 8(4):333-338.
-
(1998)
Bioorg. Med. Chem. Lett.
, vol.8
, Issue.4
, pp. 333-338
-
-
Adams, J.1
Behnke, M.2
Chen, S.3
-
42
-
-
33645173795
-
Studies on the trypanocidal activities of cysteine proteinase and proteasome inhibitors
-
MD Thesis, University of Heidelberg, Germany
-
NKEMGU-NJINKENG J: Studies on the trypanocidal activities of cysteine proteinase and proteasome inhibitors. MD Thesis, University of Heidelberg, Germany (2002).
-
(2002)
-
-
Nkemgu-Njinkeng, J.1
-
43
-
-
0032189942
-
Investigating the biological function of DNA topoisomerases in eukaryotic cells
-
NITISS JL: Investigating the biological function of DNA topoisomerases in eukaryotic cells. Biochim. Biophys. Acta (1998) 1400(1-3):63-81.
-
(1998)
Biochim. Biophys. Acta
, vol.1400
, Issue.1-3
, pp. 63-81
-
-
Nitiss, J.L.1
-
44
-
-
0032489675
-
A model for the mechanism of human topoisomerase I
-
STEWART L, REDINBO MR, QUI X, HOL WGJ, CHAMPOUX JJ: A model for the mechanism of human topoisomerase I. Science (1998) 279(5356)1534-1541.
-
(1998)
Science
, vol.279
, Issue.5356
, pp. 1534-1541
-
-
Stewart, L.1
Redinbo, M.R.2
Qui, X.3
Hol, W.G.J.4
Champoux, J.J.5
-
45
-
-
0030045003
-
Structure and mechanism of DNA topoisomerase II
-
BERGER JM, GAMBLIN SJ, HARRISON SC, WANG JC: Structure and mechanism of DNA topoisomerase II. Nature (1996) 379(6562):225-232.
-
(1996)
Nature
, vol.379
, Issue.6562
, pp. 225-232
-
-
Berger, J.M.1
Gamblin, S.J.2
Harrison, S.C.3
Wang, J.C.4
-
46
-
-
3142710896
-
Topoisomerases of kinetoplastid parasites as potential chemotherapeutic targets
-
DAS A, DASGUPTA A, SENGUPTA T, MAJUMDER HK: Topoisomerases of kinetoplastid parasites as potential chemotherapeutic targets. Trends Parasitol. (2004) 20(8):381-387.
-
(2004)
Trends Parasitol.
, vol.20
, Issue.8
, pp. 381-387
-
-
Das, A.1
Dasgupta, A.2
Sengupta, T.3
Majumder, H.K.4
-
47
-
-
0038272015
-
An unusual type IB topoisomerase from African trypanosomes
-
BODLEY AL, CHAKRABORTY AK, XIE S, BURRI C, SHAPIRO TA: An unusual type IB topoisomerase from African trypanosomes. Proc. Natl. Acad. Sci. USA (2003) 100(13):7539-7544.
-
(2003)
Proc. Natl. Acad. Sci. USA
, vol.100
, Issue.13
, pp. 7539-7544
-
-
Bodley, A.L.1
Chakraborty, A.K.2
Xie, S.3
Burri, C.4
Shapiro, T.A.5
-
48
-
-
2942536409
-
RNA interference of Trypanosoma brucei topoisomerase IB: Both subunits are essential
-
BAKSHI RP, SHAPIRO TA: RNA interference of Trypanosoma brucei topoisomerase IB: both subunits are essential. Mol. Biochem. Parasitol. (2004) 136(2):249-255.
-
(2004)
Mol. Biochem. Parasitol.
, vol.136
, Issue.2
, pp. 249-255
-
-
Bakshi, R.P.1
Shapiro, T.A.2
-
49
-
-
0035801634
-
RNA interference of a trypanosome topoisomerase II causes progressive loss of mitochondrial DNA
-
WANG Z, ENGLUND PT: RNA interference of a trypanosome topoisomerase II causes progressive loss of mitochondrial DNA. EMBO J. (2001) 20(17):4674-4683.
-
(2001)
EMBO J.
, vol.20
, Issue.17
, pp. 4674-4683
-
-
Wang, Z.1
Englund, P.T.2
-
50
-
-
0035724690
-
DNA topoisomerases as targets for anticancer drugs
-
TOPCU Z: DNA topoisomerases as targets for anticancer drugs. J. Clin. Pharm. Ther. (2001) 26(6):405-416.
-
(2001)
J. Clin. Pharm. Ther.
, vol.26
, Issue.6
, pp. 405-416
-
-
Topcu, Z.1
-
51
-
-
0028818612
-
Antitrypanosomal activity of camptothecin analogs. Structure-activity correlations
-
BODLEY AL, WANI MC, WALL ME, SHAPIRO TA: Antitrypanosomal activity of camptothecin analogs. Structure-activity correlations. Biochem. Pharmacol. (1995) 50(7):937-942.
-
(1995)
Biochem. Pharmacol.
, vol.50
, Issue.7
, pp. 937-942
-
-
Bodley, A.L.1
Wani, M.C.2
Wall, M.E.3
Shapiro, T.A.4
-
52
-
-
14844336328
-
Anti-trypanosomal activities of DNA topoisomerase inhibitors
-
DETERRING A, DUNGEY FA, THOMPSON K-T, STEVERDING D: Anti-trypanosomal activities of DNA topoisomerase inhibitors. Acta Trop. (2005) 93(3):311-316.
-
(2005)
Acta Trop.
, vol.93
, Issue.3
, pp. 311-316
-
-
Deterring, A.1
Dungey, F.A.2
Thompson, K.-T.3
Steverding, D.4
-
53
-
-
0030863434
-
Bioactivation of the anticancer agent CPT-11 to SN-38 by human hepatic microsomal carboxylesterases and the in vitro assessment of potential drug interactions
-
SLATTER JG, SU P, SAMS JP, SCHAAF LJ, WIENKERS LC: Bioactivation of the anticancer agent CPT-11 to SN-38 by human hepatic microsomal carboxylesterases and the in vitro assessment of potential drug interactions. Drug Metab. Dispos. (1997) 25(10):1157-1164.
-
(1997)
Drug Metab. Dispos.
, vol.25
, Issue.10
, pp. 1157-1164
-
-
Slatter, J.G.1
Su, P.2
Sams, J.P.3
Schaaf, L.J.4
Wienkers, L.C.5
-
54
-
-
0018137126
-
Trypanocidal activity of antitumour antibiotics and other metabolic inhibitors
-
WILLIAMSON J, SCOTT-FINNIGAN TJ: Trypanocidal activity of antitumour antibiotics and other metabolic inhibitors. Antimicrob. Agents Chemother. (1978) 13(5):735-744.
-
(1978)
Antimicrob. Agents Chemother.
, vol.13
, Issue.5
, pp. 735-744
-
-
Williamson, J.1
Scott-Finnigan, T.J.2
-
56
-
-
0034985960
-
Evaluation of quinolone derivatives for antitrypanosomal activity
-
KEISER J, BURRI C: Evaluation of quinolone derivatives for antitrypanosomal activity. Trop. Med. Int. Health (2001) 6(5):369-389.
-
(2001)
Trop. Med. Int. Health
, vol.6
, Issue.5
, pp. 369-389
-
-
Keiser, J.1
Burri, C.2
-
57
-
-
0041421172
-
Antitrypanosomal activities of fluoroquinolones with pyrrolidinyl substitutions
-
NENORTAS E, KULIKOWICZ T, BURRI C, SHAPIRO TA: Antitrypanosomal activities of fluoroquinolones with pyrrolidinyl substitutions. Antimicrob. Agents Chemother. (2003) 47(9):3015-3017.
-
(2003)
Antimicrob. Agents Chemother.
, vol.47
, Issue.9
, pp. 3015-3017
-
-
Nenortas, E.1
Kulikowicz, T.2
Burri, C.3
Shapiro, T.A.4
-
58
-
-
0024694308
-
Quinolone therapy for infections of the central nervous system
-
SCHELD WM: Quinolone therapy for infections of the central nervous system. Rev. Infect. Dis. (1989) 11(Suppl. 5):S1194-S1202.
-
(1989)
Rev. Infect. Dis.
, vol.11
, Issue.SUPPL. 5
-
-
Scheld, W.M.1
-
59
-
-
0032724638
-
The cytoskeleton of trypanosomatid parasites
-
GULL K: The cytoskeleton of trypanosomatid parasites. Ann. Rev. Microbiol. (1999) 53:629-655.
-
(1999)
Ann. Rev. Microbiol.
, vol.53
, pp. 629-655
-
-
Gull, K.1
-
60
-
-
0034611755
-
New tubulins in protozoal parasites
-
VAUGHAN S, ATTWOOD T, NAVARRO M, SCOTT V, McKEAN P, GULL K: New tubulins in protozoal parasites. Curr. Biol. (2000) 10(7):R258-R259.
-
(2000)
Curr. Biol.
, vol.10
, Issue.7
-
-
Vaughan, S.1
Attwood, T.2
Navarro, M.3
Scott, V.4
Mckean, P.5
Gull, K.6
-
61
-
-
0034894876
-
Protist tubulins: New arrivals, evolutionay relationships and insights to cytoskeletal function
-
GULL K: Protist tubulins: new arrivals, evolutionay relationships and insights to cytoskeletal function. Curr. Opin. Microbiol. (2001) 4(4):427-432.
-
(2001)
Curr. Opin. Microbiol.
, vol.4
, Issue.4
, pp. 427-432
-
-
Gull, K.1
-
62
-
-
0004389753
-
Antimicrotubule agents
-
TDR/TRY/DRUG/90.4, WHO, Geneva, Switzerland
-
GULL K: Antimicrotubule agents. In: Report of a Meeting on the Development of Drugs against Trypanosomiasis, Leishmaniasis and Chagas Disease. TDR/TRY/DRUG/90.4, WHO, Geneva, Switzerland (1990):2-13.
-
(1990)
Report of a Meeting on the Development of Drugs Against Trypanosomiasis, Leishmaniasis and Chagas Disease
, pp. 2-13
-
-
Gull, K.1
-
63
-
-
0019862535
-
Taxol, a microtubule stabilizing agent, blocks the replication of Trypanosoma cruzi
-
BAUM SG, WITTNER M, NADLER JP et al.: Taxol, a microtubule stabilizing agent, blocks the replication of Trypanosoma cruzi. Proc. Natl. Acad. Sci. USA (1981) 78(7):4571-4575.
-
(1981)
Proc. Natl. Acad. Sci. USA
, vol.78
, Issue.7
, pp. 4571-4575
-
-
Baum, S.G.1
Wittner, M.2
Nadler, J.P.3
-
64
-
-
0036293071
-
Classical ligands bind tubulin of trypanosomes and inhibit their growth in vitro
-
OCHOLA DO, PRICHARD PK, LUBEGA GW: Classical ligands bind tubulin of trypanosomes and inhibit their growth in vitro. J. Parasitol. (2002) 88(3):600-604.
-
(2002)
J. Parasitol.
, vol.88
, Issue.3
, pp. 600-604
-
-
Ochola, D.O.1
Prichard, P.K.2
Lubega, G.W.3
-
65
-
-
0028935746
-
Microtubule polarity and dynamics in the control of organelle positioning, segregation, and cytokinesis in the trypanosome cell cycle
-
ROBINSON DR, SHERWIN T, PLOUBIDOU A, BYARD EH, GULL K: Microtubule polarity and dynamics in the control of organelle positioning, segregation, and cytokinesis in the trypanosome cell cycle. J. Cell Biol. (1995) 128(6):1163-1172.
-
(1995)
J. Cell Biol.
, vol.128
, Issue.6
, pp. 1163-1172
-
-
Robinson, D.R.1
Sherwin, T.2
Ploubidou, A.3
Byard, E.H.4
Gull, K.5
-
66
-
-
0035022840
-
Dinitroaniline herbicides against protozoan parasites: The case of Trypanosoma cruzi
-
TRAUB-CSEKO YM, RAMALHO-ORTIGÃO JM, DANTAS AP, DE CASTRO SL, BARBOSA HS, DOWNING KH: Dinitroaniline herbicides against protozoan parasites: the case of Trypanosoma cruzi. Trends Parasitol. (2001) 17(3):136-141.
-
(2001)
Trends Parasitol.
, vol.17
, Issue.3
, pp. 136-141
-
-
Traub-Cseko, Y.M.1
Ramalho-Ortigão, J.M.2
Dantas, A.P.3
De Castro, S.L.4
Barbosa, H.S.5
Downing, K.H.6
-
67
-
-
0033033126
-
Effects of trifluralin on Trypanosoma cruzi in vitro and in vivo
-
ZAIDENBERG A, TOURNIER H, SCHINELLA G, MARIN G, BUSCHIAZZO H: Effects of trifluralin on Trypanosoma cruzi in vitro and in vivo. Pharmacol. Toxicol. (1999) 84(2):98-100.
-
(1999)
Pharmacol. Toxicol.
, vol.84
, Issue.2
, pp. 98-100
-
-
Zaidenberg, A.1
Tournier, H.2
Schinella, G.3
Marin, G.4
Buschiazzo, H.5
-
68
-
-
0346996811
-
Selective antimicrotuble activity of N1-phenyl-3,5-dinitro-N4,N4-di-n-propylsulfanilamide (GB-II-5) against kinetoplastid parasites
-
WERBOVETZ KA, SACKETT DL, DELFÍN D et al.: Selective antimicrotuble activity of N1-phenyl-3,5-dinitro-N4,N4-di-n-propylsulfanilamide (GB-II-5) against kinetoplastid parasites. Mol. Pharmacol. (2003) 64(6):1325-1333.
-
(2003)
Mol. Pharmacol.
, vol.64
, Issue.6
, pp. 1325-1333
-
-
Werbovetz, K.A.1
Sackett, D.L.2
Delfín, D.3
-
69
-
-
1642333024
-
4-substituted 3,4-dinitro sulfanilamides against African trypanosomes and Leishmania
-
4-substituted 3,4-dinitro sulfanilamides against African trypanosomes and Leishmania. J. Med. Chem. (2004) 47(7):1823-1832.
-
(2004)
J. Med. Chem.
, vol.47
, Issue.7
, pp. 1823-1832
-
-
Bhattacharya, G.1
Herman, J.2
Delfín, D.3
-
71
-
-
0037327813
-
Fatty acid and sterol metabolism: Potential antimicrobial targets in apicomplexan and trypanosomatid parasitic protozoa
-
ROBERTS CW, McLEOD R, RICE DW, GINGER M, CHANCE KL, GOAD LJ: Fatty acid and sterol metabolism: potential antimicrobial targets in apicomplexan and trypanosomatid parasitic protozoa. Mol. Biochem. Parasitol. (2003) 126(2):129-142.
-
(2003)
Mol. Biochem. Parasitol.
, vol.126
, Issue.2
, pp. 129-142
-
-
Roberts, C.W.1
Mcleod, R.2
Rice, D.W.3
Ginger, M.4
Chance, K.L.5
Goad, L.J.6
-
72
-
-
0035025017
-
Mechanism of action of anti-proliferative lysophospholipid analogues against the protozoan parasite Trypanosoma cruzi: Potentiation of in vitro activity by the sterol biosynthesis inhibitor ketoconazole
-
LIRA R, CONTRERAS LM, SANTA RITA RM, URBINA JA: Mechanism of action of anti-proliferative lysophospholipid analogues against the protozoan parasite Trypanosoma cruzi: potentiation of in vitro activity by the sterol biosynthesis inhibitor ketoconazole. J. Antimicrob. Chemother. (2001) 47(5):537-546.
-
(2001)
J. Antimicrob. Chemother.
, vol.47
, Issue.5
, pp. 537-546
-
-
Lira, R.1
Contreras, L.M.2
Santa Rita, R.M.3
Urbina, J.A.4
-
73
-
-
0028916661
-
Host plasma low density lipoprotein particles as an essential source of lipids for the bloodstream forms of Trypanosoma brucei
-
COPPENS I, LEVADE T, COURTOY PJ: Host plasma low density lipoprotein particles as an essential source of lipids for the bloodstream forms of Trypanosoma brucei. J. Biol. Chem. (1995) 270(11):5736-5741.
-
(1995)
J. Biol. Chem.
, vol.270
, Issue.11
, pp. 5736-5741
-
-
Coppens, I.1
Levade, T.2
Courtoy, P.J.3
-
74
-
-
0000416470
-
Receptors for the host low density lipoproteins on the hemoflagellate Trypanosoma brucei: Purification and involvement in the growth of the parasite
-
COPPENS I, BAUDHUIN P, OPPERDOES FR, COURTOY PJ: Receptors for the host low density lipoproteins on the hemoflagellate Trypanosoma brucei: purification and involvement in the growth of the parasite. Proc. Natl. Acad. Sci. USA (1988) 85(18):6753-6757.
-
(1988)
Proc. Natl. Acad. Sci. USA
, vol.85
, Issue.18
, pp. 6753-6757
-
-
Coppens, I.1
Baudhuin, P.2
Opperdoes, F.R.3
Courtoy, P.J.4
-
75
-
-
0035796796
-
The interactions of amphotericin B with various sterols in relation to its possible use in anticancer therapy
-
CHARBONNEAU C, FOURNIER I, DUFRESNE S, BARWICZ J, TANCREDE P: The interactions of amphotericin B with various sterols in relation to its possible use in anticancer therapy. Biophys. Chem. (2001) 91(2):125-133.
-
(2001)
Biophys. Chem.
, vol.91
, Issue.2
, pp. 125-133
-
-
Charbonneau, C.1
Fournier, I.2
Dufresne, S.3
Barwicz, J.4
Tancrede, P.5
-
76
-
-
0032801314
-
In vitro and in vivo activity of amphotericin B-lipid formulations against experimental Trypanosoma cruzi infections
-
YARDLEY V, CROFT SL: In vitro and in vivo activity of amphotericin B-lipid formulations against experimental Trypanosoma cruzi infections. Am. J. Trop. Med. Hyg. (1999) 61(2):193-197.
-
(1999)
Am. J. Trop. Med. Hyg.
, vol.61
, Issue.2
, pp. 193-197
-
-
Yardley, V.1
Croft, S.L.2
-
77
-
-
0034712428
-
Effect of the alkyllysophospholipids on the proliferation and differentiation of Trypanosoma cruzi
-
SANTA-RITA RM, SANTOS BARBOSA H, MEIRELLES MNSL, DE CASTRO SL: Effect of the alkyllysophospholipids on the proliferation and differentiation of Trypanosoma cruzi. Acta Trop. (2000) 75(2):219-228.
-
(2000)
Acta Trop.
, vol.75
, Issue.2
, pp. 219-228
-
-
Santa-Rita, R.M.1
Santos Barbosa, H.2
Meirelles, M.N.S.L.3
De Castro, S.L.4
-
78
-
-
0038165393
-
A strategy to reduce cardiovascular disease by more than 80%
-
WALD NJ, LAW MR: A strategy to reduce cardiovascular disease by more than 80%. Br. Med. J. (2003) 326(7404):1419.
-
(2003)
Br. Med. J.
, vol.326
, Issue.7404
, pp. 1419
-
-
Wald, N.J.1
Law, M.R.2
-
79
-
-
0025020543
-
Inhibition of Trypanosoma cruzi growth and sterol biosynthesis by lovastatin
-
FLORIN-CHRISTENSEN M, FLORIN-CHRISTENSEN J, GARIN C, ISOLA E, BRENNER RR, RASMUSSEN L: Inhibition of Trypanosoma cruzi growth and sterol biosynthesis by lovastatin. Biochem. Biophys. Res. Commun. (1990) 166(3):1441-1445.
-
(1990)
Biochem. Biophys. Res. Commun.
, vol.166
, Issue.3
, pp. 1441-1445
-
-
Florin-Christensen, M.1
Florin-Christensen, J.2
Garin, C.3
Isola, E.4
Brenner, R.R.5
Rasmussen, L.6
-
80
-
-
0027413385
-
Mevinolin (lovastatin) potentiates the antiproliferative effect of ketoconazole and terbinafine against Trypanosoma (Schizotrypanum) cruzi: In vitro and in vivo studies
-
URBINA JA, LAZARDI K, MARCHAN E et al.: Mevinolin (lovastatin) potentiates the antiproliferative effect of ketoconazole and terbinafine against Trypanosoma (Schizotrypanum) cruzi: in vitro and in vivo studies. Antimicrob. Agents Chemother. (1993) 37(3):580-591.
-
(1993)
Antimicrob. Agents Chemother.
, vol.37
, Issue.3
, pp. 580-591
-
-
Urbina, J.A.1
Lazardi, K.2
Marchan, E.3
-
81
-
-
0037116593
-
Kinetic properties and inhibition of Trypanosoma cruzi 3-hydroxy-3-methylglutaryl CoA reductase
-
HURTADO-GUERRERO R, PEÑA-DÍAZ J, MONTALVETTI A, RUIZ-PÉREZ LM, GONZÁLEZ-PACANOWSKA D: Kinetic properties and inhibition of Trypanosoma cruzi 3-hydroxy-3-methylglutaryl CoA reductase. FEBS Lett. (2002) 510(3):141-144.
-
(2002)
FEBS Lett.
, vol.510
, Issue.3
, pp. 141-144
-
-
Hurtado-Guerrero, R.1
Peña-Díaz, J.2
Montalvetti, A.3
Ruiz-Pérez, L.M.4
González-Pacanowska, D.5
-
82
-
-
1542373737
-
Mitochondrial localization of the mevalonate pathway enzyme 3-hydroxy-3-methyl-glutaryl-CoA reductase in the Trypanosomatidae
-
PEÑA-DÍAZ J, MONTALVETTI A, FLORES CL et al.: Mitochondrial localization of the mevalonate pathway enzyme 3-hydroxy-3-methyl-glutaryl-CoA reductase in the Trypanosomatidae. Mol. Biol. Cell (2004) 15(3):1356-1363.
-
(2004)
Mol. Biol. Cell
, vol.15
, Issue.3
, pp. 1356-1363
-
-
Peña-Díaz, J.1
Montalvetti, A.2
Flores, C.L.3
-
83
-
-
0035823604
-
Bisphosphonates are potent inhibitors of Trypanosoma cruzi farnesyl pyrophosphate synthase
-
MONTALVETTI A, BAILEY BN, MARTIN MB, SEVERIN GW, OLDFIELD E, DOCAMPO R: Bisphosphonates are potent inhibitors of Trypanosoma cruzi farnesyl pyrophosphate synthase. J. Biol. Chem. (2001) 276(36):33930-33937.
-
(2001)
J. Biol. Chem.
, vol.276
, Issue.36
, pp. 33930-33937
-
-
Montalvetti, A.1
Bailey, B.N.2
Martin, M.B.3
Severin, G.W.4
Oldfield, E.5
Docampo, R.6
-
84
-
-
0035866666
-
Bisphosphonates inhibit the growth of Trypanosoma brucei, Trypanosoma cruzi, Leishmania donovani, Toxoplasma gondii, and Plasmodium falciparum: A potential route to chemotherapy
-
MARTIN MB, GRIMLEY JS, LEWIS JC et al.: Bisphosphonates inhibit the growth of Trypanosoma brucei, Trypanosoma cruzi, Leishmania donovani, Toxoplasma gondii, and Plasmodium falciparum: a potential route to chemotherapy. J. Med. Chem. (2001) 44(6):909-916.
-
(2001)
J. Med. Chem.
, vol.44
, Issue.6
, pp. 909-916
-
-
Martin, M.B.1
Grimley, J.S.2
Lewis, J.C.3
-
85
-
-
0033585003
-
Trypanosoma cruzi contains major pyrophosphate stores, and its growth in vitro and in vivo is blocked by pyrophosphate analogs
-
URBINA JA, MORENO B, VIERKOTTER S et al.: Trypanosoma cruzi contains major pyrophosphate stores, and its growth in vitro and in vivo is blocked by pyrophosphate analogs. J. Biol. Chem. (1999) 274(47):33609-33615.
-
(1999)
J. Biol. Chem.
, vol.274
, Issue.47
, pp. 33609-33615
-
-
Urbina, J.A.1
Moreno, B.2
Vierkotter, S.3
-
86
-
-
1442336494
-
Selective in vitro effects of the farnesyl pyrophosphate synthase inhibitor risedronate on Trypanosoma cruzi
-
GARZONI LR, CALDERA A, MEIRELLES MNL et al.: Selective in vitro effects of the farnesyl pyrophosphate synthase inhibitor risedronate on Trypanosoma cruzi. Int. J. Antimicrob. Agents (2004) 23(3):273-285.
-
(2004)
Int. J. Antimicrob. Agents
, vol.23
, Issue.3
, pp. 273-285
-
-
Garzoni, L.R.1
Caldera, A.2
Meirelles, M.N.L.3
-
87
-
-
1442287477
-
Antiparasitic activity of risedronate in a murine model of acute Chagas' disease
-
GARZONI LR, WAGHABI MC, BAPTISTA MM et al.: Antiparasitic activity of risedronate in a murine model of acute Chagas' disease. Int. J. Antimicrob. Agents (2004) 23(3):286-290.
-
(2004)
Int. J. Antimicrob. Agents
, vol.23
, Issue.3
, pp. 286-290
-
-
Garzoni, L.R.1
Waghabi, M.C.2
Baptista, M.M.3
-
88
-
-
0034284550
-
Therapeutic approaches to bone diseases
-
RODAN GA, MARTIN TJ: Therapeutic approaches to bone diseases. Science (2000) 289(5484):1508-1514.
-
(2000)
Science
, vol.289
, Issue.5484
, pp. 1508-1514
-
-
Rodan, G.A.1
Martin, T.J.2
-
89
-
-
0036860240
-
Squalene synthase as a chemotherapeutic target in Trypanosoma cruzi and Leishmania mexicana
-
URBINA JA, CONCEPCION JL, RANGEL S, VISBAL G, LIRA R: Squalene synthase as a chemotherapeutic target in Trypanosoma cruzi and Leishmania mexicana. Mol. Biochem. Parasitol. (2002) 125(1-2):35-45.
-
(2002)
Mol. Biochem. Parasitol.
, vol.125
, Issue.1-2
, pp. 35-45
-
-
Urbina, J.A.1
Concepcion, J.L.2
Rangel, S.3
Visbal, G.4
Lira, R.5
-
90
-
-
20244386998
-
Biphenylquinuclidines as inhibitors of squalen synthase and growth of parasitic protozoa
-
ORENES LORENTE S, GÓMEZ R, JIMÉMEZ C et al.: Biphenylquinuclidines as inhibitors of squalen synthase and growth of parasitic protozoa. Bioorg. Med. Chem. (2005) 13(10): 3519-3529.
-
(2005)
Bioorg. Med. Chem.
, vol.13
, Issue.10
, pp. 3519-3529
-
-
Orenes Lorente, S.1
Gómez, R.2
Jimémez, C.3
-
91
-
-
3042570789
-
In vitro and in vivo activities of E5700 and ER-119884, two novel orally-active squalene synthase inhibitors, against Trypanosoma cruzi
-
URBINA JA, CONCEPCION JL, CLADERA A et al.: In vitro and in vivo activities of E5700 and ER-119884, two novel orally-active squalene synthase inhibitors, against Trypanosoma cruzi. Antimicrob. Agents Chemother. (2004) 48(7):2379-2387.
-
(2004)
Antimicrob. Agents Chemother.
, vol.48
, Issue.7
, pp. 2379-2387
-
-
Urbina, J.A.1
Concepcion, J.L.2
Cladera, A.3
-
92
-
-
0038778632
-
Mechanism of action of 4-phenoxyphenoxyethyl thiocyanate (WC-9) against Trypanosoma cruzi, the causative agent of Chagas' disease
-
URBINA JA, CONCEPCION JL, MONTALVETTI A, RODRIGUEZ JB, DOCAMPO R: Mechanism of action of 4-phenoxyphenoxyethyl thiocyanate (WC-9) against Trypanosoma cruzi, the causative agent of Chagas' disease. Antimicrob. Agents Chemother. (2003) 47(6):2047-2050.
-
(2003)
Antimicrob. Agents Chemother.
, vol.47
, Issue.6
, pp. 2047-2050
-
-
Urbina, J.A.1
Concepcion, J.L.2
Montalvetti, A.3
Rodriguez, J.B.4
Docampo, R.5
-
93
-
-
0023681312
-
Antiproliferative synergism of the allylamine SF-86-327 and ketoconazole on epimastogotes and amastigotes of Trypanosoma (Schizotrypanum) cruzi
-
URBINA JA, LAZARDI K, AGUIRRE T, PIRAS MM, PIRAS R: Antiproliferative synergism of the allylamine SF-86-327 and ketoconazole on epimastogotes and amastigotes of Trypanosoma (Schizotrypanum) cruzi. Antimicrob. Agents Chemother. (1988) 32(8):1237-1242.
-
(1988)
Antimicrob. Agents Chemother.
, vol.32
, Issue.8
, pp. 1237-1242
-
-
Urbina, J.A.1
Lazardi, K.2
Aguirre, T.3
Piras, M.M.4
Piras, R.5
-
94
-
-
0029687581
-
In vitro trypanocidal activities of a novel series of N,N-dimethyl-2-propen-1-amine derivative
-
DE CONTI R, RITA RM, DE SOUZA EM et al.: In vitro trypanocidal activities of a novel series of N,N-dimethyl-2-propen-1-amine derivative. Microbes (1996) 85(343):83-87.
-
(1996)
Microbes
, vol.85
, Issue.343
, pp. 83-87
-
-
De Conti, R.1
Rita, R.M.2
De Souza, E.M.3
-
95
-
-
0036849223
-
3-[4′-Bromo-(1,1′biphenyl)-4-yl]-N,N-dimethyl-3-(2-thienyl) -2-propen-1-amine: Synthesis, cytotoxicity, and leishmanicidal, trypanocidal and antimycobacterial activities
-
DE SOUZA AO, HEMERLY FP, BUSOLLO AC et al.: 3-[4′-Bromo-(1,1′biphenyl)-4-yl]-N,N- dimethyl-3-(2-thienyl)-2-propen-1-amine: synthesis, cytotoxicity, and leishmanicidal, trypanocidal and antimycobacterial activities. J. Antimicrob. Chemother. (2002) 50(5):629-637.
-
(2002)
J. Antimicrob. Chemother.
, vol.50
, Issue.5
, pp. 629-637
-
-
De Souza, A.O.1
Hemerly, F.P.2
Busollo, A.C.3
-
96
-
-
12544252330
-
2-Propen-1-amine derivatives and their synthetic intermediates: Activity against pathogenic trypanosomatids
-
DE SOUZA AO, HEMERLY FP, GOMES-CARDOSO L et al.: 2-Propen-1-amine derivatives and their synthetic intermediates: activity against pathogenic trypanosomatids. J. Chemother. (2004) 16(6):530-533.
-
(2004)
J. Chemother.
, vol.16
, Issue.6
, pp. 530-533
-
-
De Souza, A.O.1
Hemerly, F.P.2
Gomes-Cardoso, L.3
-
97
-
-
15044358173
-
Trypanocidal activity of 2-propen-1-amine derivatives on trypomastigotes culture and in animal model
-
OLIVEIRA DA, PEREIRA DG, FERNANDES AMAP et al.: Trypanocidal activity of 2-propen-1-amine derivatives on trypomastigotes culture and in animal model. Parasitol. Res. (2005) 95(3):161-166.
-
(2005)
Parasitol. Res.
, vol.95
, Issue.3
, pp. 161-166
-
-
Oliveira, D.A.1
Pereira, D.G.2
Fernandes, A.M.A.P.3
-
98
-
-
0035076959
-
Potent anti-Trypanosoma cruzi activities of oxidosqualene cyclase inhibitors
-
BUCKNER FS, GRIFFEN JH, WILSON AJ, VAN VOORHIS WC: Potent anti-Trypanosoma cruzi activities of oxidosqualene cyclase inhibitors. Antimicrob. Agents Chemother. (2001) 45(4):1210-1215.
-
(2001)
Antimicrob. Agents Chemother.
, vol.45
, Issue.4
, pp. 1210-1215
-
-
Buckner, F.S.1
Griffen, J.H.2
Wilson, A.J.3
Van Voorhis, W.C.4
-
99
-
-
0023760272
-
Overview of medically importmant antifungal azole derivatives
-
FROMTLING RA: Overview of medically importmant antifungal azole derivatives. Clin. Microbiol. Rev. (1988) 1(2):187-217.
-
(1988)
Clin. Microbiol. Rev.
, vol.1
, Issue.2
, pp. 187-217
-
-
Fromtling, R.A.1
-
100
-
-
0020590530
-
Ketoconazole protects against infection with Trypanosoma cruzi in a murine model
-
McCABE RE, ARAUJO FG, REMINGTON JS: Ketoconazole protects against infection with Trypanosoma cruzi in a murine model. Am. J. Trop. Hyg. (1983) 32(5):960-962.
-
(1983)
Am. J. Trop. Hyg.
, vol.32
, Issue.5
, pp. 960-962
-
-
Mccabe, R.E.1
Araujo, F.G.2
Remington, J.S.3
-
101
-
-
0021150439
-
Ketoconazole inhibition of intracellular multiplication of Trypanosoma cruzi and protection of mice against lethal infection with the organism
-
McCABE RE, REMINGTON JS, ARAUJO FG: Ketoconazole inhibition of intracellular multiplication of Trypanosoma cruzi and protection of mice against lethal infection with the organism. J. Infect. Dis. (1984) 150(4):594-601.
-
(1984)
J. Infect. Dis.
, vol.150
, Issue.4
, pp. 594-601
-
-
Mccabe, R.E.1
Remington, J.S.2
Araujo, F.G.3
-
102
-
-
0343527887
-
A combination of benznidazole and ketoconazole enhances efficacy of chemotherapy of experimental Chagas' disease
-
ARAÚJO MSS, MARTINS-FILHO OA, PEREIRA MES, BRENER Z: A combination of benznidazole and ketoconazole enhances efficacy of chemotherapy of experimental Chagas' disease. J. Antimicrob. Chemother. (2000) 45(6):819-824.
-
(2000)
J. Antimicrob. Chemother.
, vol.45
, Issue.6
, pp. 819-824
-
-
Araújo, M.S.S.1
Martins-Filho, O.A.2
Pereira, M.E.S.3
Brener, Z.4
-
103
-
-
0027484860
-
An experimental and clinical assay with ketoconazole in the treatment of Chagas disease
-
BRENER Z, CANCADO JR, GALVAO LM et al.: An experimental and clinical assay with ketoconazole in the treatment of Chagas disease. Mem. Inst. Oswaldo Cruz (1993) 88(1):149-153.
-
(1993)
Mem. Inst. Oswaldo Cruz
, vol.88
, Issue.1
, pp. 149-153
-
-
Brener, Z.1
Cancado, J.R.2
Galvao, L.M.3
-
104
-
-
17944384088
-
Treatment of chronic Chagas' disease with itraconazole and allopurinol
-
APT W, AGUILERA X, ARRIBADA A et al.: Treatment of chronic Chagas' disease with itraconazole and allopurinol. Am. J. Trop. Med. Hyg. (1998) 59(1):133-138.
-
(1998)
Am. J. Trop. Med. Hyg.
, vol.59
, Issue.1
, pp. 133-138
-
-
Apt, W.1
Aguilera, X.2
Arribada, A.3
-
105
-
-
0031761201
-
Induction of resistance to azole drugs in Trypanosoma cruzi
-
BUCKNER FS, WILSON AJ, WHITE TC, VAN VOORHIS WC: Induction of resistance to azole drugs in Trypanosoma cruzi. Antimicrob. Agents Chemother. (1998) 42(12):3245-3250.
-
(1998)
Antimicrob. Agents Chemother.
, vol.42
, Issue.12
, pp. 3245-3250
-
-
Buckner, F.S.1
Wilson, A.J.2
White, T.C.3
Van Voorhis, W.C.4
-
106
-
-
9444291409
-
Cure of short- And long-term experimental Chagas' disease using D0870
-
URBINA JA, PAYARES G, MOLINA J et al.: Cure of short- and long-term experimental Chagas' disease using D0870. Science (1996) 273(5277):969-971.
-
(1996)
Science
, vol.273
, Issue.5277
, pp. 969-971
-
-
Urbina, J.A.1
Payares, G.2
Molina, J.3
-
108
-
-
0033987127
-
Activities of the triazole derivative SCH 56592 (posaconazole) against drug-resistant strains of the protozoan parasite Trypanosoma (Schizotrypanum) cruzi in immunocompetent and immunosuppressed murine hosts
-
MOLINA J, MARTINS-FILHO O, BRENER Z, ROMANHA AJ, LOEBENBERG D, URBINA JA: Activities of the triazole derivative SCH 56592 (posaconazole) against drug-resistant strains of the protozoan parasite Trypanosoma (Schizotrypanum) cruzi in immunocompetent and immunosuppressed murine hosts. Antimicrob. Agents Chemother. (2000) 44(1):150-155.
-
(2000)
Antimicrob. Agents Chemother.
, vol.44
, Issue.1
, pp. 150-155
-
-
Molina, J.1
Martins-Filho, O.2
Brener, Z.3
Romanha, A.J.4
Loebenberg, D.5
Urbina, J.A.6
-
109
-
-
0033844976
-
In vitro antiproliferative effects and mechanism of action of the new triazole derivative UR-9825 against the protozoan parasite Trypanosoma (Schizotrypanum) cruzi
-
URBINA JA, LIRA R, VISBAL G, BARTROLI J: In vitro antiproliferative effects and mechanism of action of the new triazole derivative UR-9825 against the protozoan parasite Trypanosoma (Schizotrypanum) cruzi. Antimicrob. Agents Chemother. (2000) 44(9):2498-2502.
-
(2000)
Antimicrob. Agents Chemother.
, vol.44
, Issue.9
, pp. 2498-2502
-
-
Urbina, J.A.1
Lira, R.2
Visbal, G.3
Bartroli, J.4
-
110
-
-
7244219956
-
Activity of the new triazole derivative albaconazole against Trypanosoma (Schizotrypanum) cruzi in dog hosts
-
GUEDES PMM, URBINA JA, DE LANA M et al.: Activity of the new triazole derivative albaconazole against Trypanosoma (Schizotrypanum) cruzi in dog hosts. Antimicrob. Agents Chemother. (2004) 48(11):4286-4292.
-
(2004)
Antimicrob. Agents Chemother.
, vol.48
, Issue.11
, pp. 4286-4292
-
-
Guedes, P.M.M.1
Urbina, J.A.2
De Lana, M.3
-
111
-
-
0037220818
-
Parasitological cure of acute and chronic experimental Chagas disease using the long-acting experimental triazole TAK-187. Activity against drug-resistant Trypanosoma cruzi strains
-
URBINA JA, PAYARES G, SANOJA C et al.: Parasitological cure of acute and chronic experimental Chagas disease using the long-acting experimental triazole TAK-187. Activity against drug-resistant Trypanosoma cruzi strains. Int. J. Antimicrob. Agents (2003) 21(1):39-48.
-
(2003)
Int. J. Antimicrob. Agents
, vol.21
, Issue.1
, pp. 39-48
-
-
Urbina, J.A.1
Payares, G.2
Sanoja, C.3
-
112
-
-
0037220817
-
In vitro and in vivo activities of ravuconazole on Typanosoma cruzi, the causative agents of Chagas disease
-
URBINA JA, PAYARES G, SANOJA C, LIRA R, ROMAN HA AJ: In vitro and in vivo activities of ravuconazole on Typanosoma cruzi, the causative agents of Chagas disease. Int. J. Antimicrob. Agents (2003) 21(1):27-38.
-
(2003)
Int. J. Antimicrob. Agents
, vol.21
, Issue.1
, pp. 27-38
-
-
Urbina, J.A.1
Payares, G.2
Sanoja, C.3
Lira, R.4
Roman, H.A.A.J.5
-
113
-
-
10744230525
-
A class of sterol 14-demethylase inhibitors as anti-Trypanosoma cruzi agents
-
BUCKNER F, YOKOYAMA K, LOCKMAN J et al.: A class of sterol 14-demethylase inhibitors as anti-Trypanosoma cruzi agents. Proc. Natl. Acad. Sci. USA (2003) 100(25):15149-14153.
-
(2003)
Proc. Natl. Acad. Sci. USA
, vol.100
, Issue.25
, pp. 14153-15149
-
-
Buckner, F.1
Yokoyama, K.2
Lockman, J.3
-
114
-
-
0142124194
-
Azasterols as inhibitors of sterol 24-methyltransferase in Leishmania species and Trypanosoma cruzi
-
MAGARACI F, JIMENEZ CJ, RODRIGUES C et al.: Azasterols as inhibitors of sterol 24-methyltransferase in Leishmania species and Trypanosoma cruzi. J. Med. Chem. (2003) 46(22):4714-4727.
-
(2003)
J. Med. Chem.
, vol.46
, Issue.22
, pp. 4714-4727
-
-
Magaraci, F.1
Jimenez, C.J.2
Rodrigues, C.3
-
115
-
-
3342962349
-
Novel azasterols as potential agents for treatment of leishmaniasis and trypanosomiasis
-
ORENES LORENTE S, RODRIGUEZ JCF, JIMÉNEZ CJ et al.: Novel azasterols as potential agents for treatment of leishmaniasis and trypanosomiasis. Antimicrob. Agents Chemother. (2004) 48(8):2937-2950.
-
(2004)
Antimicrob. Agents Chemother.
, vol.48
, Issue.8
, pp. 2937-2950
-
-
Orenes Lorente, S.1
Rodriguez, J.C.F.2
Jiménez, C.J.3
-
116
-
-
0142258171
-
Leishmaniasis - Current chemotherapy and recent advances in the search for novel drugs
-
CROFT SL, COOMBS GH: Leishmaniasis - current chemotherapy and recent advances in the search for novel drugs. Trends Parasitol. (2003) 19(11):502-508.
-
(2003)
Trends Parasitol.
, vol.19
, Issue.11
, pp. 502-508
-
-
Croft, S.L.1
Coombs, G.H.2
-
117
-
-
0030481123
-
The activities of four anticancer alkyllysophospholipids against Leishmania donovani, Trypanosoma cruzi and Trypanosoma brucei
-
CROFT S, SNOWDON D, YARDLEY V: The activities of four anticancer alkyllysophospholipids against Leishmania donovani, Trypanosoma cruzi and Trypanosoma brucei. J. Antimicrob. Chemother. (1996) 38(6):1041-1047.
-
(1996)
J. Antimicrob. Chemother.
, vol.38
, Issue.6
, pp. 1041-1047
-
-
Croft, S.1
Snowdon, D.2
Yardley, V.3
-
118
-
-
0036840473
-
Proinflammatory and cytotoxic effects of hexadecylphosphocholine (miltefosine) against drug-resistant strains of Trypanosoma cruzi
-
SARAIVA VB, GIBALDI D, PREVIATO JO et al.: Proinflammatory and cytotoxic effects of hexadecylphosphocholine (miltefosine) against drug-resistant strains of Trypanosoma cruzi. Antimicrob. Agents Chemother. (2002) 46(11):3472-3477.
-
(2002)
Antimicrob. Agents Chemother.
, vol.46
, Issue.11
, pp. 3472-3477
-
-
Saraiva, V.B.1
Gibaldi, D.2
Previato, J.O.3
-
119
-
-
18844381913
-
Antiproliferative synergy of lysophospholipid analogues and ketoconazole against Trypanosoma cruzi (Kinetoplastida: Trypanosomatidae): Cellular and ultrastructural analysis
-
SANTA-RITA RM, LIRA R, BARBOSA HS, URBINA JA, DE CASTRO SL: Antiproliferative synergy of lysophospholipid analogues and ketoconazole against Trypanosoma cruzi (Kinetoplastida: Trypanosomatidae): cellular and ultrastructural analysis. J. Antimicrob. Chemother. (2005) 55(5):780-784.
-
(2005)
J. Antimicrob. Chemother.
, vol.55
, Issue.5
, pp. 780-784
-
-
Santa-Rita, R.M.1
Lira, R.2
Barbosa, H.S.3
Urbina, J.A.4
De Castro, S.L.5
-
120
-
-
0345073644
-
Protein farnesyl and N-myristol transferases: Piggy-back medicinal chemistry targets for the development of antitrypanosomatid and antimalarial therapeutics
-
GELB MH, VAN VORHEIS WC, BUCKNER FS et al.: Protein farnesyl and N-myristol transferases: piggy-back medicinal chemistry targets for the development of antitrypanosomatid and antimalarial therapeutics. Mol. Biochem. Parasitol. (2003) 126(2):155-163.
-
(2003)
Mol. Biochem. Parasitol.
, vol.126
, Issue.2
, pp. 155-163
-
-
Gelb, M.H.1
Van Vorheis, W.C.2
Buckner, F.S.3
-
121
-
-
0037136025
-
Isothiazole dioxides: Synthesis and inhibition of Trypanosoma brucei protein farnesyltransferase
-
CLERICI F, GELMI ML, YOKOYAMA K et al.: Isothiazole dioxides: synthesis and inhibition of Trypanosoma brucei protein farnesyltransferase. Bioorg. Med. Chem. Lett. (2002) 12(16):2217-2220.
-
(2002)
Bioorg. Med. Chem. Lett.
, vol.12
, Issue.16
, pp. 2217-2220
-
-
Clerici, F.1
Gelmi, M.L.2
Yokoyama, K.3
-
122
-
-
9144248974
-
Design and synthesis of peptidomimetic protein farnesyltransferase inhibitors as antiTrypanosoma brucei agents
-
OHKANDA J, BUCKNER FS, LOCKMAN JW et al.: Design and synthesis of peptidomimetic protein farnesyltransferase inhibitors as antiTrypanosoma brucei agents. J. Med. Chem. (2004) 47(2):432-445.
-
(2004)
J. Med. Chem.
, vol.47
, Issue.2
, pp. 432-445
-
-
Ohkanda, J.1
Buckner, F.S.2
Lockman, J.W.3
-
123
-
-
2942532638
-
Quinoxaline N,N-dioxide derivatives and related compounds as growth inhibitors of Trypanosoma cruzi. Structure-activity relationships
-
AGUIRRE G, CERECETTO H, DI MAIO R et al.: Quinoxaline N,N-dioxide derivatives and related compounds as growth inhibitors of Trypanosoma cruzi. Structure-activity relationships. Bioorg. Med. Chem. Lett. (2004) 14(14):3835-3839.
-
(2004)
Bioorg. Med. Chem. Lett.
, vol.14
, Issue.14
, pp. 3835-3839
-
-
Aguirre, G.1
Cerecetto, H.2
Di Maio, R.3
-
124
-
-
0036146669
-
Gluthathione derivatives active against Trypanosoma brucei rhodesiense and T. brucei brucei in vitro
-
DAUNES S, D'SILVA C: Gluthathione derivatives active against Trypanosoma brucei rhodesiense and T. brucei brucei in vitro. Antimicrob. Agents Chemother. (2002) 46(2):434-437.
-
(2002)
Antimicrob. Agents Chemother.
, vol.46
, Issue.2
, pp. 434-437
-
-
Daunes, S.1
D'silva, C.2
-
125
-
-
0035907476
-
Novel alkylpolyamine analogues that posses both antitrypanosomal and antimicrosporidial activity
-
ZOU Y, WU Z, SIRISOMA N et al.: Novel alkylpolyamine analogues that posses both antitrypanosomal and antimicrosporidial activity. Bioorg. Med. Chem. Lett. (2001) 11(12):1613-1617.
-
(2001)
Bioorg. Med. Chem. Lett.
, vol.11
, Issue.12
, pp. 1613-1617
-
-
Zou, Y.1
Wu, Z.2
Sirisoma, N.3
-
126
-
-
0035846173
-
Synthesis and biological evaluation of s-triazine substituted polyamines as potential new antitrypanosomal drugs
-
KLENKE B, STEWART M, BARRETT MP, BRUN R, GILBERT IH: Synthesis and biological evaluation of s-triazine substituted polyamines as potential new antitrypanosomal drugs. J. Med. Chem. (2001) 44(21):3440-3452.
-
(2001)
J. Med. Chem.
, vol.44
, Issue.21
, pp. 3440-3452
-
-
Klenke, B.1
Stewart, M.2
Barrett, M.P.3
Brun, R.4
Gilbert, I.H.5
-
127
-
-
1842779964
-
Bisguanidine, bis(2-aminoimidazoline), and polyamine derivatives as potent and selective chemotherapeutic agents against Trypanosoma brucei rhodesiense. Synthesis and in vitro evaluation
-
DARDONVILLE C, BRUN R: Bisguanidine, bis(2-aminoimidazoline), and polyamine derivatives as potent and selective chemotherapeutic agents against Trypanosoma brucei rhodesiense. Synthesis and in vitro evaluation. J. Med. Chem. (2004) 47(9):2296-2307.
-
(2004)
J. Med. Chem.
, vol.47
, Issue.9
, pp. 2296-2307
-
-
Dardonville, C.1
Brun, R.2
-
128
-
-
0037038329
-
Synthesis and evaluation of analogues of 5′-([(Z)-4-amino-2-butenyl]methylamino)-5′-deoxyadenosine as inhibitor of tumor cell growth, trypanosomal growth, and HIV-1 infectivity
-
MARASCO CJ JR, KRAMER DL, MILLAR J et al.: Synthesis and evaluation of analogues of 5′-([(Z)-4-amino-2- butenyl]methylamino)-5′-deoxyadenosine as inhibitor of tumor cell growth, trypanosomal growth, and HIV-1 infectivity. J. Med. Chem. (2002) 45(23):5112-5122.
-
(2002)
J. Med. Chem.
, vol.45
, Issue.23
, pp. 5112-5122
-
-
Marasco Jr., C.J.1
Kramer, D.L.2
Millar, J.3
-
129
-
-
0035866694
-
New synthesis of benzo-δ-carbolines, crytolepines, and their salts: In vitro cytotoxic, antiplasmodial, and antitrypanosomal activities of δ-carbolines, benzo-δ-carbolines, and cryptolepines
-
ARZEL E, ROCCA P, GRELLIER P et al.: New synthesis of benzo-δ-carbolines, crytolepines, and their salts: in vitro cytotoxic, antiplasmodial, and antitrypanosomal activities of δ-carbolines, benzo-δ-carbolines, and cryptolepines. J. Med. Chem. (2001) 44(6):949-960.
-
(2001)
J. Med. Chem.
, vol.44
, Issue.6
, pp. 949-960
-
-
Arzel, E.1
Rocca, P.2
Grellier, P.3
-
130
-
-
0035037935
-
In vitro and in vivo activities of aminoadamantane and aminoalkylcyclohexane derivatives against Trypanosoma brucei
-
KELLY JM, QUACK G, MILES MM: In vitro and in vivo activities of aminoadamantane and aminoalkylcyclohexane derivatives against Trypanosoma brucei. Antimicrob. Agents Chemother. (2001) 45(5):1360-1366.
-
(2001)
Antimicrob. Agents Chemother.
, vol.45
, Issue.5
, pp. 1360-1366
-
-
Kelly, J.M.1
Quack, G.2
Miles, M.M.3
-
131
-
-
0036009204
-
Benzo[1,2-c]1,2,5-oxadiazole N-oxide derivatives as potential antitrypanosomal drugs. Structure-activity relationships
-
AGUIRRE G, CERECETTO H, DI MAIO R et al.: Benzo[1,2-c]1,2,5-oxadiazole N-oxide derivatives as potential antitrypanosomal drugs. Structure-activity relationships. Part II. Arch. Pharm. (Weinheim) (2002) 335(1):15-21.
-
(2002)
Arch. Pharm. (Weinheim)
, vol.335
, Issue.1 PART II
, pp. 15-21
-
-
Aguirre, G.1
Cerecetto, H.2
Di Maio, R.3
-
132
-
-
0242493920
-
Prolylisoxazoles: Potent inhibitors of prolyloligopeptidase with antitrypanosomal activity
-
BAL G, VAN DER VEKEN P, ANTONOV D et al.: Prolylisoxazoles: potent inhibitors of prolyloligopeptidase with antitrypanosomal activity. Bioorg. Med. Chem. Lett. (2003) 13(17):2875-2878.
-
(2003)
Bioorg. Med. Chem. Lett.
, vol.13
, Issue.17
, pp. 2875-2878
-
-
Bal, G.1
Van Der Veken, P.2
Antonov, D.3
-
133
-
-
0842308202
-
New 4-aminobicyclo[2.2.2]octane derivatives and their activities against Plasmodium falciparum and Trypanosoma b. rhodesiense
-
SEEBACHER W, BRUN R, WEIS R: New 4-aminobicyclo[2.2.2]octane derivatives and their activities against Plasmodium falciparum and Trypanosoma b. rhodesiense. Eur. J. Pharm. Sci. (2004) 21(2-3):225-233.
-
(2004)
Eur. J. Pharm. Sci.
, vol.21
, Issue.2-3
, pp. 225-233
-
-
Seebacher, W.1
Brun, R.2
Weis, R.3
-
134
-
-
14144252391
-
Antiprotozoal activities of new bicycle[2.2.2]octan-2-imines and esters of bicycle [2.2.2]octan-2-ols
-
SEEBACHER W, SCHLAPPER C, BRUN R, KAISER M, SAF R, WEIS R: Antiprotozoal activities of new bicycle[2.2.2]octan-2-imines and esters of bicycle [2.2.2]octan-2-ols. Eur. J. Pharm. Sci. (2005) 24(4):281-289.
-
(2005)
Eur. J. Pharm. Sci.
, vol.24
, Issue.4
, pp. 281-289
-
-
Seebacher, W.1
Schlapper, C.2
Brun, R.3
Kaiser, M.4
Saf, R.5
Weis, R.6
-
135
-
-
0342293303
-
Synthesis and antitrypanosomal evaluation of E-isomers of 5-nitro-2-furaldehyde and 5-nitrothiophene-2-carboxaldehyde semicarbazone derivatives. Structure-activity relationships
-
CERECETTO H, DI MAIO R, GONZÁLEZ M et al.: Synthesis and antitrypanosomal evaluation of E-isomers of 5-nitro-2-furaldehyde and 5-nitrothiophene-2-carboxaldehyde semicarbazone derivatives. Structure-activity relationships. Eur. J. Med. Chem. (2000) 35(3):343-350.
-
(2000)
Eur. J. Med. Chem.
, vol.35
, Issue.3
, pp. 343-350
-
-
Cerecetto, H.1
Di Maio, R.2
González, M.3
-
136
-
-
0036891274
-
Antitrypanosomal activities and cytotoxicity of 5-nitro-2-furancarbohydrazides
-
MILLET R, MASS L, LANDRY V, SERGHERAERT C, DAVIOUT-CHARVET E: Antitrypanosomal activities and cytotoxicity of 5-nitro-2-furancarbohydrazides. Bioorg. Med. Chem. Lett. (2002) 12(24):3601-3604.
-
(2002)
Bioorg. Med. Chem. Lett.
, vol.12
, Issue.24
, pp. 3601-3604
-
-
Millet, R.1
Mass, L.2
Landry, V.3
Sergheraert, C.4
Daviout-Charvet, E.5
-
137
-
-
10744230611
-
Synthesis and in vitro evaluation of potential antichagasic hydroxymethylnitrofurazone (NFOH-121): A new nitofurazone prodrug
-
CHUNG M-C, GÜIDO RVC, MARTINELLI TF et al.: Synthesis and in vitro evaluation of potential antichagasic hydroxymethylnitrofurazone (NFOH-121): a new nitofurazone prodrug. Bioorg. Med. Chem. (2003) 11(22):4779-4783.
-
(2003)
Bioorg. Med. Chem.
, vol.11
, Issue.22
, pp. 4779-4783
-
-
Chung, M.-C.1
Güido, R.V.C.2
Martinelli, T.F.3
-
138
-
-
2142821417
-
Trypanocidal activity of melamine-based nitroheterocycles
-
STEWART M, BUENO GJ, BALIANI A et al.: Trypanocidal activity of melamine-based nitroheterocycles. Antimicrob. Agents Chemother. (2004) 48(5):1733-1738.
-
(2004)
Antimicrob. Agents Chemother.
, vol.48
, Issue.5
, pp. 1733-1738
-
-
Stewart, M.1
Bueno, G.J.2
Baliani, A.3
-
139
-
-
4444312101
-
In vitro activity and mechanism of action against the protozoan parasite Trypanosoma cruzi of 5-nitrofuryl containing thiosemicarbazones
-
AGUIRRE G, BOIANI L, CERECETTO H et al.: In vitro activity and mechanism of action against the protozoan parasite Trypanosoma cruzi of 5-nitrofuryl containing thiosemicarbazones. Bioorg. Med. Chem. (2004) 12(18):4885-4893.
-
(2004)
Bioorg. Med. Chem.
, vol.12
, Issue.18
, pp. 4885-4893
-
-
Aguirre, G.1
Boiani, L.2
Cerecetto, H.3
-
140
-
-
13944280211
-
Synthesis and in vitro antitrypanosomal activity of novel nifurtimox analogues
-
POZAS R, CARBALLO J, CASTRO C, RUBIO J: Synthesis and in vitro antitrypanosomal activity of novel nifurtimox analogues. Bioorg. Med. Chem. Lett. (2005) 15(5):1417-1421.
-
(2005)
Bioorg. Med. Chem. Lett.
, vol.15
, Issue.5
, pp. 1417-1421
-
-
Pozas, R.1
Carballo, J.2
Castro, C.3
Rubio, J.4
-
141
-
-
0142028913
-
Synthesis and antiprotozoal activity of aza-analogues of furamidine
-
ISMAIL MA, BRUN R, EASTERBROOK JD, TANIOUS FA, WILSON WD, BOYKIN DW: Synthesis and antiprotozoal activity of aza-analogues of furamidine. J. Med. Chem. (2003) 46(22):4761-4769.
-
(2003)
J. Med. Chem.
, vol.46
, Issue.22
, pp. 4761-4769
-
-
Ismail, M.A.1
Brun, R.2
Easterbrook, J.D.3
Tanious, F.A.4
Wilson, W.D.5
Boykin, D.W.6
-
142
-
-
3042552194
-
Novel dicationic imidazo[1,2-a]pyridines and 5,6,7,8-tetrahydro-imidazo[1,2-a]pyridines as antiprotozoal agents
-
ISMAIL AM, BRUN R, WENZLER T, TANIOUS FA, WILSON WD, BOYKIN DW: Novel dicationic imidazo[1,2-a]pyridines and 5,6,7,8-tetrahydro-imidazo[1,2-a]pyridines as antiprotozoal agents. J. Med. Chem. (2004) 47(14):3658-3664.
-
(2004)
J. Med. Chem.
, vol.47
, Issue.14
, pp. 3658-3664
-
-
Ismail, A.M.1
Brun, R.2
Wenzler, T.3
Tanious, F.A.4
Wilson, W.D.5
Boykin, D.W.6
-
143
-
-
3843134198
-
O-alkoxyamidine prodrugs of furamidine: In vitro transport and microsomal metabolism as indicators of in vivo efficacy in a mouse model of Trypanosoma brucei rhodesiense infection
-
ANSEDE JH, ANBAZHAGAN M, BRUN R, EASTERBROOK JD, HALL JE, BOYKIN DW: O-alkoxyamidine prodrugs of furamidine: in vitro transport and microsomal metabolism as indicators of in vivo efficacy in a mouse model of Trypanosoma brucei rhodesiense infection. J. Med. Chem. (2004) 47(17):4335-4338.
-
(2004)
J. Med. Chem.
, vol.47
, Issue.17
, pp. 4335-4338
-
-
Ansede, J.H.1
Anbazhagan, M.2
Brun, R.3
Easterbrook, J.D.4
Hall, J.E.5
Boykin, D.W.6
-
144
-
-
4544241506
-
Dicationic biphenyl benzimidazole derivatives as antiprotozoal agents
-
ISMAIL MA, BRUN R, WENZLER T, TANIOUS FA, WILSON WD, BOYKIN DW: Dicationic biphenyl benzimidazole derivatives as antiprotozoal agents. Bioorg. Med. Chem. (2004) 12(20):5405-5413.
-
(2004)
Bioorg. Med. Chem.
, vol.12
, Issue.20
, pp. 5405-5413
-
-
Ismail, M.A.1
Brun, R.2
Wenzler, T.3
Tanious, F.A.4
Wilson, W.D.5
Boykin, D.W.6
-
145
-
-
3042819882
-
Natural products active against African trypanosomes: A step towards new drugs
-
HOET S, OPPERDOES F, BRUN R, QUETIN-LECLERCQJ: Natural products active against African trypanosomes: a step towards new drugs. Nat. Prod. Rep. (2004) 21(3):353-364.
-
(2004)
Nat. Prod. Rep.
, vol.21
, Issue.3
, pp. 353-364
-
-
Hoet, S.1
Opperdoes, F.2
Brun, R.3
Quetin-Leclerc, Q.J.4
-
146
-
-
0037866531
-
The efficacy of ascufuranone in a consecutive treatment on Trypanosoma brucei brucei in mice
-
YABU Y, YOSHIDA A, SUZUKI T et al.: The efficacy of ascufuranone in a consecutive treatment on Trypanosoma brucei brucei in mice. Parasitol. Int. (2003) 52(2):155-164.
-
(2003)
Parasitol. Int.
, vol.52
, Issue.2
, pp. 155-164
-
-
Yabu, Y.1
Yoshida, A.2
Suzuki, T.3
|