-
1
-
-
34648833337
-
Phenylimidazole derivatives of 4-pyridone as dual inhibitors of bacterial enoyl-acyl carrier protein reductases FabI and FabK
-
Kitagawa, H.; Ozawa, T.; Takahata, S.; Iida, M.; Saito, J.; Yamada, M. Phenylimidazole derivatives of 4-pyridone as dual inhibitors of bacterial enoyl-acyl carrier protein reductases FabI and FabK. J. Med. Chem., 2007, 50, 4710-4720.
-
(2007)
J. Med. Chem
, vol.50
, pp. 4710-4720
-
-
Kitagawa, H.1
Ozawa, T.2
Takahata, S.3
Iida, M.4
Saito, J.5
Yamada, M.6
-
2
-
-
50249162070
-
Design and synthesis of novel thioether-linked carbapenem-oxazolidinone hybrids as potential antimicrobial agents
-
Wang, J; Huang, J.; Wu, Y.; Hai, L.; Wang, G. Design and synthesis of novel thioether-linked carbapenem-oxazolidinone hybrids as potential antimicrobial agents. Lett. Org. Chem., 2008, 5, 336-341.
-
(2008)
Lett. Org. Chem
, vol.5
, pp. 336-341
-
-
Wang, J.1
Huang, J.2
Wu, Y.3
Hai, L.4
Wang, G.5
-
3
-
-
51849112827
-
Novel dual-targeting benzimidazole urea inhibitors of dna gyrase and topoisomerase IV possessing potent antibacterial activity: Intelligent design and evolution through the judicious use of structureguided design and structure-activity relationships
-
Charifson, P.S.; Grillot, A.; Grossman, T.H.; Parsons, J.D.; Badia, M.; Bellon, S.; Deininger, D.D.; Drumm, J.E.; Gross, C.H.; LeTiran, A.; Liao, Y.; Mani, N.; Nicolau, D.P.; Perola, E.; Ronkin, S.; Shannon, D.; Swenson, L.L.; Tang, Q.; Tessier, P.R.; Tian, S.; Trudeau, M.; Wang, T.; Wei, Y.; Zhang, H.; Stamos, D. Novel dual-targeting benzimidazole urea inhibitors of dna gyrase and topoisomerase IV possessing potent antibacterial activity: intelligent design and evolution through the judicious use of structureguided design and structure-activity relationships. J. Med. Chem., 2008, 51, 5243-5263.
-
(2008)
J. Med. Chem
, vol.1
, pp. 243-5263
-
-
Charifson, P.S.1
Grillot, A.2
Grossman, T.H.3
Parsons, J.D.4
Badia, M.5
Bellon, S.6
Deininger, D.D.7
Drumm, J.E.8
Gross, C.H.9
Letiran, A.10
Liao, Y.11
Mani, N.12
Nicolau, D.P.13
Perola, E.14
Ronkin, S.15
Shannon, D.16
Swenson, L.L.17
Tang, Q.18
Tessier, P.R.19
Tian, S.20
Trudeau, M.21
Wang, T.22
Wei, Y.23
Zhang, H.24
Stamos, D.25
more..
-
4
-
-
38949086122
-
New insights for multifactorial disease therapy: The challenge of the symbiotic drugs
-
Barreiro, E.J.; Fraga, C.A.M. New insights for multifactorial disease therapy: The challenge of the symbiotic drugs. Curr. Drug Ther., 2008, 3, 1-13.
-
(2008)
Curr. Drug Ther
, vol.3
, pp. 1-13
-
-
Barreiro, E.J.1
Fraga, C.A.M.2
-
5
-
-
34250160226
-
Dual action-based approaches to antibacterial agents
-
Bremmer, J.B.; Ambrus, J.I.; Samosorn, S. Dual action-based approaches to antibacterial agents. Curr. Med. Chem., 2007, 14, 1459-1477.
-
(2007)
Curr. Med. Chem
, vol.14
, pp. 1459-1477
-
-
Bremmer, J.B.1
Ambrus, J.I.2
Samosorn, S.3
-
6
-
-
27144449695
-
Designed multiple ligands. an emerging drug discovery paradigm
-
Morphy, R.; Rankovic, Z. Designed multiple ligands. an emerging drug discovery paradigm. J. Med. Chem., 2005, 48, 6523-6543.
-
(2005)
J. Med. Chem
, vol.48
, pp. 6523-6543
-
-
Morphy, R.1
Rankovic, Z.2
-
7
-
-
65249160092
-
Design, synthesis, and evaluation of novel fluoroquinolone-aminoglycoside hybrid antibiotics
-
Pokrovskaya, V.; Belakhov, V.; Hainrichson, M.; Yaron, S.; Baasov, T. Design, synthesis, and evaluation of novel fluoroquinolone-aminoglycoside hybrid antibiotics. J. Med. Chem., 2009, 52, 2243-2254.
-
(2009)
J. Med. Chem
, vol.52
, pp. 2243-2254
-
-
Pokrovskaya, V.1
Belakhov, V.2
Hainrichson, M.3
Yaron, S.4
Baasov, T.5
-
8
-
-
34547484265
-
Molecular hybridization: A useful tool in the design of new drug prototypes
-
Viegas-Junior, C.; Danuello, A.; Bolzani, V.S.; Barreiro, E.J.; Fraga, C.A.M. Molecular hybridization: A useful tool in the design of new drug prototypes. Curr. Med. Chem., 2007, 14, 1829-1852.
-
(2007)
Curr. Med. Chem
, vol.14
, pp. 1829-1852
-
-
Viegas-Junior, C.1
Danuello, A.2
Bolzani, V.S.3
Barreiro, E.J.4
Fraga, C.A.M.5
-
9
-
-
67649094515
-
Drug hybridization strategies: Before or after lead identification?
-
Fraga, C.A.M. Drug hybridization strategies: Before or after lead identification? Exp. Opin. Drug Discov., 2009, 4, 605-609.
-
(2009)
Exp. Opin. Drug Discov
, vol.4
, pp. 605-609
-
-
Fraga, C.A.M.1
-
10
-
-
14844348264
-
Molecular insights into aminoglycoside action and resistance
-
Magnet, S.; Blanchard, J.S. Molecular insights into aminoglycoside action and resistance. Chem. Rev., 2005, 105, 477-498.
-
(2005)
Chem. Rev
, vol.105
, pp. 477-498
-
-
Magnet, S.1
Blanchard, J.S.2
-
11
-
-
0242711908
-
Aminoglycoside antibiotic-inactivating enzymes in actinomycetes similar to those present in clinical isolates of antibiotic-resistant bacteria
-
Benveniste, R.; Davies, J. aminoglycoside antibiotic-inactivating enzymes in actinomycetes similar to those present in clinical isolates of antibiotic-resistant bacteria. Proc. Natl. Acad. Sci. USA, 1973, 70, 2276-2280.
-
(1973)
Proc. Natl. Acad. Sci. USA
, vol.70
, pp. 2276-2280
-
-
Benveniste, R.1
Davies, J.2
-
12
-
-
0038778553
-
Mechanisms of quinolone action and microbial response
-
Hawkey, P.M. Mechanisms of quinolone action and microbial response. J. Antimicrob. Chemother., 2003, 51 (Suppl. 1), 29-35.
-
(2003)
J. Antimicrob. Chemother
, vol.51
, Issue.SUPPL. 1
, pp. 29-35
-
-
Hawkey, P.M.1
-
13
-
-
0014170214
-
Interaction of streptothricin and related antibiotics with nucleic acids
-
Zimmer, C.; Triebel, H.; Thrum, H. Interaction of streptothricin and related antibiotics with nucleic acids. Biochim. Biophys. Acta., 1967, 145, 742-751.
-
(1967)
Biochim. Biophys. Acta
, vol.145
, pp. 742-751
-
-
Zimmer, C.1
Triebel, H.2
Thrum, H.3
-
14
-
-
0035293206
-
Linezolid: An oxazolidinone antimicrobial agent
-
Fung, H.B.; Kirschenbaum, H.L.; Ojofeitimi, B.O. Linezolid: an oxazolidinone antimicrobial agent. Clin. Ther., 2001, 23, 356-391.
-
(2001)
Clin. Ther
, vol.23
, pp. 356-391
-
-
Fung, H.B.1
Kirschenbaum, H.L.2
Ojofeitimi, B.O.3
-
15
-
-
0035928419
-
Linezolid resistance in a clinical isolate of Staphylococcus aureus
-
Tsiodras, S.; Gold, H.S.; Sakoulas, G.; Eliopoulos, G.M.; Wennersten, C.; Venkataraman, L.; Moellering, R.C. Linezolid resistance in a clinical isolate of Staphylococcus aureus. Lancet, 2001, 358, 207-208.
-
(2001)
Lancet
, vol.358
, pp. 207-208
-
-
Tsiodras, S.1
Gold, H.S.2
Sakoulas, G.3
Eliopoulos, G.M.4
Wennersten, C.5
Venkataraman, L.6
Moellering, R.C.7
-
16
-
-
10744224468
-
Novel oxazolidinone-quinolone hybrid antimicrobials
-
Gordeev, M.F.; Hackbarth, C.; Barbachyn, M.R.; Banitt, L.S.; Gage, J.R.; Luehr, G.W.; Gomez, M.; Trias, J.; Morin, S.E.; Zurenko, G.E.; Parker, C.N.; Evans, J.M.; White, R.J.; Patel, D.V. Novel oxazolidinone-quinolone hybrid antimicrobials. Bioorg. Med. Chem. Lett., 2003, 13, 4213-4216.
-
(2003)
Bioorg. Med. Chem. Lett
, vol.13
, pp. 4213-4216
-
-
Gordeev, M.F.1
Hackbarth, C.2
Barbachyn, M.R.3
Banitt, L.S.4
Gage, J.R.5
Luehr, G.W.6
Gomez, M.7
Trias, J.8
Morin, S.E.9
Zurenko, G.E.10
Parker, C.N.11
Evans, J.M.12
White, R.J.13
Patel, D.V.14
-
17
-
-
0037447946
-
Design, synthesis and biological evaluation of oxazolidinone-quinolone hybrids
-
Hubschwerlen, C.; Specklin, J-L.; Sigwalt, C.; Schroeder, S.; Locher, H.H. Design, synthesis and biological evaluation of oxazolidinone-quinolone hybrids. Bioorg. Med. Chem., 2003, 11, 2313-2319.
-
(2003)
Bioorg. Med. Chem
, vol.11
, pp. 2313-2319
-
-
Hubschwerlen, C.1
Specklin, J.-L.2
Sigwalt, C.3
Schroeder, S.4
Locher, H.H.5
-
18
-
-
17544367317
-
Inhibition of graphic-ketoacyl-acyl carrier protein synthase III (FabH) by acyl-acyl carrier protein in Escherichia coli
-
Heath, R.J.; Rock, C.O. Inhibition of graphic-ketoacyl-acyl carrier protein synthase III (FabH) by acyl-acyl carrier protein in Escherichia coli. J. Biol. Chem., 1996, 271, 10996-11000.
-
(1996)
J. Biol. Chem
, vol.271
, pp. 10996-11000
-
-
Heath, R.J.1
Rock, C.O.2
-
19
-
-
33746892678
-
AG205, a novel agent directed against FabK of Streptococcus pneumonia
-
Takahata, S.; Iida, M; Osaki, Y.; Saito, J.; Kitagawa, H.; Ozawa, T.; Yoshida, T.; Hoshiko, S. AG205, a novel agent directed against FabK of Streptococcus pneumonia. Antimicrob. Agents. Chemother., 2006, 50, 2869-2871.
-
(2006)
Antimicrob. Agents. Chemother
, vol.50
, pp. 2869-2871
-
-
Takahata, S.1
Iida, M.2
Osaki, Y.3
Saito, J.4
Kitagawa, H.5
Ozawa, T.6
Yoshida, T.7
Hoshiko, S.8
-
20
-
-
33845298658
-
4- Pyridone derivatives as new inhibitors of bacterial enoyl-ACP reductase FabI
-
Kitagawa, H.; Kumura, K.; Takahata, S.; Iida, M.; Atsumi, K. 4- Pyridone derivatives as new inhibitors of bacterial enoyl-ACP reductase FabI. Bioorg. Med. Chem., 2007, 15, 1106-1116.
-
(2007)
Bioorg. Med. Chem
, vol.15
, pp. 1106-1116
-
-
Kitagawa, H.1
Kumura, K.2
Takahata, S.3
Iida, M.4
Atsumi, K.5
-
21
-
-
64049088223
-
Discovery of dual inhibitors targeting both HIV-1 capsid and human cyclophilin A to inhibit the assembly and uncoating of the viral capsid
-
Li, J.; Tan, Z.; Tang, S.; Hewlett, I.; Pang, R.; He, M.; He, S.; Tian, B.; Chen, K.; Yang, M. Discovery of dual inhibitors targeting both HIV-1 capsid and human cyclophilin A to inhibit the assembly and uncoating of the viral capsid. Bioorg. Med. Chem., 2009, 17, 3177-3188.
-
(2009)
Bioorg. Med. Chem
, vol.17
, pp. 3177-3188
-
-
Li, J.1
Tan, Z.2
Tang, S.3
Hewlett, I.4
Pang, R.5
He, M.6
He, S.7
Tian, B.8
Chen, K.9
Yang, M.10
-
22
-
-
0141706723
-
Mutations E44D and V118I in the reverse transcriptase of HIV-1 play distinct mechanistic roles in dual resistance to AZT and 3TC
-
Girouard, M.; Diallo, K.; Marchand, B.; McCormick, S.; Götte, M. Mutations E44D and V118I in the reverse transcriptase of HIV-1 play distinct mechanistic roles in dual resistance to AZT and 3TC. J. Biol. Chem., 2003, 278, 34403-34410.
-
(2003)
J. Biol. Chem
, vol.278
, pp. 34403-34410
-
-
Girouard, M.1
Diallo, K.2
Marchand, B.3
McCormick, S.4
Götte, M.5
-
23
-
-
30144438891
-
Update on HAART in HIV
-
Yeni, P. Update on HAART in HIV. J. Hepatol., 2006, 44(Suppl), S100-S103.
-
(2006)
J. Hepatol
, vol.44
, Issue.SUPPL.
-
-
Yeni, P.1
-
24
-
-
0037391631
-
Adherence to HAART Regimens
-
Chesney, M. Adherence to HAART Regimens. AIDS Patient Care ST., 2003, 17, 169-177.
-
(2003)
AIDS Patient Care ST
, vol.17
, pp. 169-177
-
-
Chesney, M.1
-
25
-
-
51449117426
-
Design of hybrid inhibitors to HIV-1 protease
-
Zhang, D.W.; Huang, P.L.; Lee-Huang, S.; Zhang, J.Z.H. Design of hybrid inhibitors to HIV-1 protease. J. Theor. Comput. Chem., 2008, 7, 485-503.
-
(2008)
J. Theor. Comput. Chem
, vol.7
, pp. 485-503
-
-
Zhang, D.W.1
Huang, P.L.2
Lee-Huang, S.3
Zhang, J.Z.H.4
-
26
-
-
0032483022
-
Three new structures of the core domain of HIV-1 integrase: An active site that binds magnesium
-
Goldgur, Y.; Dyda, F.; Hickman, A.B.; Jenkins, T.M.; Craigie, R.; Davies, D.R. Three new structures of the core domain of HIV-1 integrase: An active site that binds magnesium. Proc. Natl. Acad. Sci. USA, 1998, 95, 9150-9154.
-
(1998)
Proc. Natl. Acad. Sci. USA
, vol.95
, pp. 9150-9154
-
-
Goldgur, Y.1
Dyda, F.2
Hickman, A.B.3
Jenkins, T.M.4
Craigie, R.5
Davies, D.R.6
-
27
-
-
0002296754
-
Reverse transcriptase and the generation of viral DNA
-
RetroViruses; Coffin, J.M., Hughes, S.H., Varmus, H.E., Eds., Plainview, NY
-
Telesnitsky, A.; Goff, S.P. Reverse transcriptase and the generation of viral DNA. In RetroViruses; Coffin, J.M., Hughes, S.H., Varmus, H.E., Eds.; Cold Spring Harbor Laboratory Press: Plainview, NY, 1997; pp 121-160.
-
(1997)
Cold Spring Harbor Laboratory Press
, pp. 121-160
-
-
Telesnitsky, A.1
Goff, S.P.2
-
28
-
-
6944235757
-
Closely related antiretroviral agents as inhibitors of two HIV-1 enzymes, ribonuclease h and integrase: Killing two birds with one stone
-
Andréola, M. Closely related antiretroviral agents as inhibitors of two HIV-1 enzymes, ribonuclease h and integrase: Killing two birds with one stone. Curr. Pharm. Des., 2004, 10, 3713-3723.
-
(2004)
Curr. Pharm. Des
, vol.10
, pp. 3713-3723
-
-
Andréola, M.1
-
29
-
-
41649107669
-
Design and synthesis of dual inhibitors of HIV reverse transcriptase and integrase: Introducing a diketoacid functionality into delavirdine
-
Wang, Z.; Vince, R. Design and synthesis of dual inhibitors of HIV reverse transcriptase and integrase: Introducing a diketoacid functionality into delavirdine. Bioorg. Med. Chem., 2008, 16, 3587- 3595.
-
(2008)
Bioorg. Med. Chem
, vol.16
, pp. 3587-3595
-
-
Wang, Z.1
Vince, R.2
-
30
-
-
58149083480
-
Design, synthesis, and biological evaluation of a series of 2-hydroxyisoquinoline-1,3(2H,4H)-diones as dual inhibitors of human immunodeficiency virus type 1 integrase and the reverse transcriptase RNase H domain
-
Billamboz, M.; Bailly, F.; Barreca, M.L.; De Luca, L.; Mouscadet, J-F.; Calmels, C.; Marie-Line Andréola, M-L.; Witvrouw, M.; Christ, F.; Debyser, Z.; Cotelle, P. Design, synthesis, and biological evaluation of a series of 2-hydroxyisoquinoline-1,3(2H,4H)-diones as dual inhibitors of human immunodeficiency virus type 1 integrase and the reverse transcriptase RNase H domain. J. Med. Chem., 2008, 51, 7717-7730.
-
(2008)
J. Med. Chem
, vol.51
, pp. 7717-7730
-
-
Billamboz, M.1
Bailly, F.2
Barreca, M.L.3
de Luca, L.4
Mouscadet, J.-F.5
Calmels, C.6
Marie-Line andréola, M.-L.7
Witvrouw, M.8
Christ, F.9
Debyser, Z.10
Cotelle, P.11
-
31
-
-
0023941761
-
New antifungal antibiotics, benanomicins A and B from an actinomycete
-
Tokyo
-
Takeuchi, T.; Hara, T.; Naganawa, H.; Okada, M.; Hamada, M.; Umezawa, H.; Gomi, S.; Sezaki, M.; Kondo, S. New antifungal antibiotics, benanomicins A and B from an actinomycete. J. Antibiot. (Tokyo), 1988, 41, 807- 811.
-
(1988)
J. Antibiot
, vol.41
, pp. 807-811
-
-
Takeuchi, T.1
Hara, T.2
Naganawa, H.3
Okada, M.4
Hamada, M.5
Umezawa, H.6
Gomi, S.7
Sezaki, M.8
Kondo, S.9
-
32
-
-
0025362647
-
B and C: New antifungal antibiotics
-
Tokyo
-
Oki, T.; Tenmyo, O.; Hirano, M.; Tomatsu, K.; Kamei, H. Pradimicins A, B and C: new antifungal antibiotics. J. Antibiot. (Tokyo), 1990, 43, 763-770.
-
(1990)
J. Antibiot
, vol.43
, pp. 763-770
-
-
Oki, T.1
Tenmyo, O.2
Hirano, M.3
Tomatsu, K.4
Kamei, H.5
Pradimicins, A.6
-
33
-
-
37849020692
-
Madurahydroxylactone derivatives as dual inhibitors of human immunodeficiency virus type 1 Integrase and RNase H
-
Marchand, C.; Beutler, J.A.; Wamiru, A.; Budihas, S.; Möllmann, U.; Heinisch, L.; Mellors, J.W.; Le Grice, S.F.; Pommier, Y. Madurahydroxylactone derivatives as dual inhibitors of human immunodeficiency virus type 1 Integrase and RNase H. Antimicrob. Agents Chemother., 2008, 52, 361-364.
-
(2008)
Antimicrob. Agents Chemother
, vol.52
, pp. 361-364
-
-
Marchand, C.1
Beutler, J.A.2
Wamiru, A.3
Budihas, S.4
Möllmann, U.5
Heinisch, L.6
Mellors, J.W.7
Le Grice, S.F.8
Pommier, Y.9
-
34
-
-
72249097281
-
Neglected tropical diseases: Multitarget- directed ligands in the search for novel lead candidates against Trypanosoma and Leishmania
-
Cavalli, M.; Bolognesi, M.L. Neglected tropical diseases: Multitarget- directed ligands in the search for novel lead candidates against Trypanosoma and Leishmania. J. Med. Chem., 2009, 52, 7339-7359.
-
(2009)
J. Med. Chem
, vol.52
, pp. 7339-7359
-
-
Cavalli, M.1
Bolognesi, M.L.2
-
35
-
-
34548630777
-
Lost in translation
-
Butler, D. Lost in translation. Nature, 2007, 449, 158-159.
-
(2007)
Nature
, vol.449
, pp. 158-159
-
-
Butler, D.1
-
36
-
-
34548422845
-
Control of neglected tropical diseases
-
Hotez, P.J.; Molyneux, D.H.; Fenwick, A.; Kumaresan, J.; Sachs, S.E.; Sachs, J.D.; Savioli, L. Control of neglected tropical diseases. N. Engl. J. Med., 2007, 357, 1018-1027.
-
(2007)
N. Engl. J. Med
, vol.357
, pp. 1018-1027
-
-
Hotez, P.J.1
Molyneux, D.H.2
Fenwick, A.3
Kumaresan, J.4
Sachs, S.E.5
Sachs, J.D.6
Savioli, L.7
-
37
-
-
18044365378
-
The Chemotherapy of Chagas' disease
-
Paulino, M.; Iribarne, F.; Dubin, M.; Aguilera-Morales, S.; Tapia, O.; Stoppani, A.O. The Chemotherapy of Chagas' disease: An overview. Mini-Rev. Med. Chem., 2005, 5, 499-519.
-
(2005)
An Overview. Mini-Rev. Med. Chem
, vol.5
, pp. 499-519
-
-
Paulino, M.1
Iribarne, F.2
Dubin, M.3
Aguilera-Morales, S.4
Tapia, O.5
Stoppani, A.O.6
-
38
-
-
34247167023
-
Trypanosomatidae peptidases: A Target for drug development
-
Vermelho, A.B.; De Simone, S.G.; d'Avila-Levy, C.M.; Santos, A.L.S.; Melo, A.C.N.; Silva-Junior, F.P.; Bon, E.P.S.; Branquinha, M.H. Trypanosomatidae peptidases: A Target for drug development. Curr. Enzyme Inhib., 2007, 3, 19-48.
-
(2007)
Curr. Enzyme Inhib
, vol.3
, pp. 19-48
-
-
Vermelho, A.B.1
de Simone, S.G.2
D'avila-Levy, C.M.3
Santos, A.L.S.4
Melo, A.C.N.5
Silva-Junior, F.P.6
Bon, E.P.S.7
Branquinha, M.H.8
-
39
-
-
0034772197
-
A policy for leishmaniasis with respect to the prevention and control of drug resistance
-
Bryceson, A. A policy for leishmaniasis with respect to the prevention and control of drug resistance. Trop. Med. Int. Health, 2001, 6, 928-934.
-
(2001)
Trop. Med. Int. Health
, vol.6
, pp. 928-934
-
-
Bryceson, A.1
-
40
-
-
70349643110
-
Discovery of novel antileishmanial agents in an attempt to synthesize pentamidine-aplysinopsin hybrid molecule
-
Porwal, S.; Chauhan, S.S.; Chauhan, P.M.S.; Shakya, N.; Verma, A.; Gupta, S. Discovery of novel antileishmanial agents in an attempt to synthesize pentamidine-aplysinopsin hybrid molecule. J. Med. Chem., 2009, 52, 5793-5802.
-
(2009)
J. Med. Chem
, vol.2
, pp. 5793-5802
-
-
Porwal, S.1
Chauhan, S.S.2
Chauhan, P.M.S.3
Shakya, N.4
Verma, A.5
Gupta, S.6
-
41
-
-
74049100572
-
Practical and efficient synthesis of pyrano[3,2-c]pyridone, pyrano[4,3-b]pyran and their hybrids with nucleoside as potential antiviral and antileishmanial agents
-
Fan, X.; Feng, D.; Qu, Y.; Zhang, X.; Wang, J.; Loiseau, P.M.; Andrei, G.; Snoeck, R.; De Clercq, E. Practical and efficient synthesis of pyrano[3,2-c]pyridone, pyrano[4,3-b]pyran and their hybrids with nucleoside as potential antiviral and antileishmanial agents. Bioorg. Med. Chem., 2010, 20, 809-813.
-
(2010)
Bioorg. Med. Chem
, vol.20
, pp. 809-813
-
-
Fan, X.1
Feng, D.2
Qu, Y.3
Zhang, X.4
Wang, J.5
Loiseau, P.M.6
Andrei, G.7
Snoeck, R.8
de Clercq, E.9
-
42
-
-
0032918170
-
Perspectives of non-nucleoside reverse transcriptase inhibitors (NNRTIs) in the therapy of HIV-1 infection
-
De Clercq, E. Perspectives of non-nucleoside reverse transcriptase inhibitors (NNRTIs) in the therapy of HIV-1 infection. II Farmaco, 1999, 54, 26-45.
-
(1999)
II Farmaco
, vol.54
, pp. 26-45
-
-
de Clercq, E.1
-
43
-
-
25144441808
-
Discovery of 4-aryl-4H-chromenes as a new series of apoptosis inducers using a cell- and caspase-based high-throughput screening assay. 2. Structure-activity relationships of the 7- and 5-, 6-, 8- positions
-
Kemnitzer, W.; Kasibhatla, S.; Jiang, S.; Zhang, H.; Zhao, J.; Jia, S.; Xu, L.; Crogan-Grundy, C.; Denis, R.; Barriault, N.; Vaillancourt, L.; Charron, S.; Dodd, J.; Attardo, G.; Labrecque, D.; Lamothe, S.; Gourdeau, H.; Tseng, B.; Drewe, J.; Cai, S. X. Discovery of 4-aryl-4H-chromenes as a new series of apoptosis inducers using a cell- and caspase-based high-throughput screening assay. 2. Structure-activity relationships of the 7- and 5-, 6-, 8- positions. Bioorg. Med. Chem. Lett., 2005, 15, 4745-4751.
-
(2005)
Bioorg. Med. Chem. Lett
, vol.15
, pp. 4745-4751
-
-
Kemnitzer, W.1
Kasibhatla, S.2
Jiang, S.3
Zhang, H.4
Zhao, J.5
Jia, S.6
Xu, L.7
Crogan-Grundy, C.8
Denis, R.9
Barriault, N.10
Vaillancourt, L.11
Charron, S.12
Dodd, J.13
Attardo, G.14
Labrecque, D.15
Lamothe, S.16
Gourdeau, H.17
Tseng, B.18
Drewe, J.19
Cai, S.X.20
more..
-
44
-
-
0028004138
-
Chemical and bioactive constituents from Zanthoxylum simulans
-
Chen, I.S.; Wu, S.J.; Tsai, I.L.; Wu, T.S.; Pezzuto, J.M.; Lu, M.C.; Chai, H.; Suh, N.; Teng, C.M. Chemical and bioactive constituents from Zanthoxylum simulans. J. Nat. Prod., 1994, 57, 1206-1211.
-
(1994)
J. Nat. Prod
, vol.57
, pp. 1206-1211
-
-
Chen, I.S.1
Wu, S.J.2
Tsai, I.L.3
Wu, T.S.4
Pezzuto, J.M.5
Lu, M.C.6
Chai, H.7
Suh, N.8
Teng, C.M.9
-
45
-
-
0037142343
-
Synthesis and structure-activity relationship study of potent trypanocidal thio semicarbazone inhibitors of the trypanosomal cysteine protease cruzain
-
Du, X.; Gui, C.; Hansell, E.; Doyle, P.S.; Caffrey, C.R.; Holler, T.P.; McKerrow, J.H.; Cohen, F.E. Synthesis and structure-activity relationship study of potent trypanocidal thio semicarbazone inhibitors of the trypanosomal cysteine protease cruzain. J. Med. Chem., 2002, 45, 2695-2707.
-
(2002)
J. Med. Chem
, vol.45
, pp. 2695-2707
-
-
Du, X.1
Gui, C.2
Hansell, E.3
Doyle, P.S.4
Caffrey, C.R.5
Holler, T.P.6
McKerrow, J.H.7
Cohen, F.E.8
-
46
-
-
33847669811
-
Second generation of 5-ethenylbenzofuroxan derivatives as inhibitors of Trypanosoma cruzi growth: Synthesis, biological evaluation, and structure-activity relationships
-
Porcal, W.; Hernández, P.; Aguirre, G.; Boiani, L.; Boiani, M.; Merlino, A.; Ferreira, A.; DiMaio, R.; Castro, A.; González, M.; Cerecetto, H. Second generation of 5-ethenylbenzofuroxan derivatives as inhibitors of Trypanosoma cruzi growth: Synthesis, biological evaluation, and structure-activity relationships. Bioorg. Med. Chem., 2007, 15, 2768-2781.
-
(2007)
Bioorg. Med. Chem
, vol.15
, pp. 2768-2781
-
-
Porcal, W.1
Hernández, P.2
Aguirre, G.3
Boiani, L.4
Boiani, M.5
Merlino, A.6
Ferreira, A.7
Dimaio, R.8
Castro, A.9
González, M.10
Cerecetto, H.11
-
47
-
-
47349092118
-
New trypanocidal hybrid compounds from the association of hydrazone moieties and benzofuroxan heterocycle
-
Porcal, W.; Hernández, P.; Boiani, L.; Boiani, M.; Ferreira, A.; Chidichimo, A.; Cazzulo, J.J.; Olea-Azar, C.; González, M.; Cerecetto, H. New trypanocidal hybrid compounds from the association of hydrazone moieties and benzofuroxan heterocycle. Bioorg. Med. Chem., 2008, 16, 6995-7004.
-
(2008)
Bioorg. Med. Chem
, vol.16
, pp. 6995-7004
-
-
Porcal, W.1
Hernández, P.2
Boiani, L.3
Boiani, M.4
Ferreira, A.5
Chidichimo, A.6
Cazzulo, J.J.7
Olea-Azar, C.8
González, M.9
Cerecetto, H.10
-
48
-
-
8844278475
-
Synthesis and antitrypanosomal profile of new functionalized 1,3,4-thiadiazole-2-arylhydrazone derivatives, designed as non-mutagenic megazol analogues
-
Carvalho, S.A.; Silva, E.F.; Santa-Rita, R.M.; Castro, S.L.; Fraga, C.A.M. Synthesis and antitrypanosomal profile of new functionalized 1,3,4-thiadiazole-2-arylhydrazone derivatives, designed as non-mutagenic megazol analogues. Bioorg. Med. Chem. Lett., 2004, 14, 5967-5970.
-
(2004)
Bioorg. Med. Chem. Lett
, vol.14
, pp. 5967-5970
-
-
Carvalho, S.A.1
Silva, E.F.2
Santa-Rita, R.M.3
Castro, S.L.4
Fraga, C.A.M.5
-
49
-
-
38049065444
-
Studies toward the structural optimization of new brazilizone-related trypanocidal 1,3,4-thiadiazole-2-aryl hydrazone derivatives
-
Carvalho, S.A.; Lopes, F.A.S.; Salomão, K.; Romeiro, N.C.; Wardell, S.M. S.V.; Castro, S.L.; Silva, E.F.; Fraga, C.A.M. Studies toward the structural optimization of new brazilizone-related trypanocidal 1,3,4-thiadiazole-2-aryl hydrazone derivatives. Bioorg. Med. Chem. Lett., 2008, 16, 413-421.
-
(2008)
Bioorg. Med. Chem. Lett
, vol.16
, pp. 413-421
-
-
Carvalho, S.A.1
Lopes, F.A.S.2
Salomão, K.3
Romeiro, N.C.4
Wardell, S.M.S.V.5
Castro, S.L.6
Silva, E.F.7
Fraga, C.A.M.8
-
50
-
-
0020323313
-
A nitroimidazole-thiadiazole derivative with curative action in experimental Trypanosoma cruzi infections
-
Filardi, L.S.; Brener, Z. A nitroimidazole-thiadiazole derivative with curative action in experimental Trypanosoma cruzi infections. Ann. Trop. Med. Parasitol., 1982, 76, 293-297.
-
(1982)
Ann. Trop. Med. Parasitol
, vol.76
, pp. 293-297
-
-
Filardi, L.S.1
Brener, Z.2
-
51
-
-
0028803902
-
Aromatic guanyl hydrazones: Synthesis, structural studies and in vitro activity against Trypanosoma cruzi
-
Messeder, J.C.; Tinoco, L.W.; Figueroa-Villar, J.D.; Souza, E.M.; Santa Rita, R.; de Castro, S.L. Aromatic guanyl hydrazones: Synthesis, structural studies and in vitro activity against Trypanosoma cruzi. Bioorg. Med. Chem. Lett., 1995, 5, 3079-3084.
-
(1995)
Bioorg. Med. Chem. Lett
, vol.5
, pp. 3079-3084
-
-
Messeder, J.C.1
Tinoco, L.W.2
Figueroa-Villar, J.D.3
Souza, E.M.4
Santa, R.R.5
de Castro, S.L.6
-
52
-
-
79954426740
-
-
unpublished results
-
Fraga, C.A.M., unpublished results.
-
-
-
Fraga, C.A.M.1
-
53
-
-
0021716851
-
Mechanism of action, spectrum of activity, pharmacokinetics, drug interations, adverse reactions and therapeutic use
-
Van Tyle, J.H. Ketoconazole: Mechanism of action, spectrum of activity, pharmacokinetics, drug interations, adverse reactions and therapeutic use. Pharmacotheraphy., 1984, 4, 343-373.
-
(1984)
Pharmacotheraphy
, vol.4
, pp. 343-373
-
-
Tyle, V.1
Ketoconazole, J.H.2
-
54
-
-
50349101947
-
NO-donors. Part 17: Synthesis and antimicrobial activity of novel ketoconazole-NO-donor hybrid compounds
-
Konter, J.; Möllmann, U.; Lehmann, J. NO-donors. Part 17: Synthesis and antimicrobial activity of novel ketoconazole-NO-donor hybrid compounds. Bioorg. Med. Chem., 2008, 16, 8294-8300.
-
(2008)
Bioorg. Med. Chem
, vol.16
, pp. 8294-8300
-
-
Konter, J.1
Möllmann, U.2
Lehmann, J.3
-
55
-
-
0030030305
-
Effects of nifedipine, metronidazole, and nitric oxide donors on spore germination and cell culture infection of the microsporidia Encephalitozoon hellem and Encephalitozoon intestinalis. Antimicrob
-
He, Q.; Leitch, G.J.; Visvesvara, G.S.; Wallace, S. Effects of nifedipine, metronidazole, and nitric oxide donors on spore germination and cell culture infection of the microsporidia Encephalitozoon hellem and Encephalitozoon intestinalis. Antimicrob. Agents Chemother., 1996, 40, 179-185.
-
(1996)
Agents Chemother
, vol.40
, pp. 179-185
-
-
He, Q.1
Leitch, G.J.2
Visvesvara, G.S.3
Wallace, S.4
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