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Volumn 84, Issue , 2014, Pages 395-403

Synthesis and biological evaluation of 2,3-dihydroimidazo[1,2-a] benzimidazole derivatives against Leishmania donovani and Trypanosoma cruzi

Author keywords

2,3 Dihydroimidazo 1, 2 a benzimidazole; Anti parasitic activity; Chagas disease; Leishmaniasis

Indexed keywords

2,3 DIHYDROIMIDAZO[1,2 A]BENZIMIDAZOLE DERIVATIVE; 9 (3,5 DIMETHYLBENZYL) 2,9 DIHYDRO 3H BENZO[D]IMIDAZO [1,2 A]IMIDAZOLE; 9 (4 CYANOBENZYL) 3,9 DIHYDRO 2H BENZO[D]IMIDAZO[1,2 A] IMIDAZOLE; 9 (4 CYCLOHEXYLBENZYL) 2,9 DIHYDRO 3H BENZO[D]IMIDAZO [1,2 A]IMIDAZOLE; 9 (4 ETHYLBENZYL) 2,3 DIHYDROIMIDAZO[1,2 A]BENZIMIDAZOLE; 9 (4 ISOPROPYLBENZYL) 2,9 DIHYDRO 3H BENZO[D]IMIDAZO[1,2 A]IMIDAZOLE; 9 (4 PHENOXYBENZYL) 2,9 DIHYDRO 3H BENZO[D]IMIDAZO[1,2 A]IMIDAZOLE; 9 (4 PHENYLBENZYL) 2,3 DIHYDROIMIDAZO[1,2 A]BENZIMIDAZOLE; 9 (4 TERT BUTYLPHENOXYETHYL) 2,3 DIHYDROIMIDAZO[1,2 A]BENZIMIDAZOLE; 9 [3 (METHYLSULFONYLL)BENZYL] 2,9 DIHYDRO 3H BENZO[D]IMIDAZO [1,2 A]IMIDAZOLE; 9 [3 (TERT BUTYL)BENZYL] 2,9 DIHYDRO 3H BENZO[D]IMIDAZO [1,2 A]IMIDAZOLE; 9 [3 (TRIFLUOROMETHOXY)BENZYL] 3,9 DIHYDRO 2H BENZO[D]IMIDAZO [1,2 A]IMIDAZOLE; 9 [4 (TERT BUTYL)BENZYL] 6 CHLORO 3,9 DIHYDRO 2H BENZO[D] IMIDAZO[1,2 A]IMIDAZOLE; 9 [4 (TERT BUTYL)BENZYL] 6 FLUORO 2,9 DIHYDRO 3H BENZO[D] IMIDAZO[1,2 A]IMIDAZOLE; 9 [4 (TERT BUTYL)BENZYL] 6 METHYL 3,9 DIHYDRO 3H BENZO[D] IMIDAZO[1,2 A]IMIDAZOLE; 9 [4 (TERT BUTYL)BENZYL] 6,7 DIMETHYL 3,9 DIHYDRO 2H BENZO[D] IMIDAZO[1,2 A]IMIDAZOLE; 9 [4 (TERT BUTYL)PHENETHYL] 2,9 DIHYDRO 3H BENZO[D]IMIDAZO[1,2 A]IMIDAZOLE; 9 [[2',6' DIFLUORO (1,1' BIPHENYL) 4 YL]METHYL] 2,9 DIHYDRO 3H BENZO[D]IMIDAZO[1,2 A]IMIDAZOLE; 9 [[4' (TRIFLUOROMETHOXY) (1,1' BIPHENYL) 4 YL]METHYL] 3,9 DIHYDRO 2H BENZO[D]IMIDAZO[1,2 A]IMIDAZOLE; 9 [[4' CHLORO (1,1' BIPHENYL) 4 YL]METHYL] 3,9 DIHYDRO 2H BENZO[D]IMIDAZO[1,2 A]IMIDAZOLE; 9 [[4' METHOXY (1,1' BIPHENYL) 4 YL]METHYL] 3,9 DIHYDRO 2H BENZO[D]IMIDAZO[1,2 A]IMIDAZOLE; 9 [[4', FLUORO (1,1' BIPHENYL) 4 YL]METHYL] 3,9 DIHYDRO 2H BENZO[D]IMIDAZO[1,2 A]IMIDAZOLE; 9 [[4', METHYL (1,1' BIPHENYL) 4 YL]METHYL] 3,9 DIHYDRO 2H BENZO[D]IMIDAZO[1,2 A]IMIDAZOLE; ANTILEISHMANIAL AGENT; ANTITRYPANOSOMAL AGENT; BENZIMIDAZOLE DERIVATIVE; UNCLASSIFIED DRUG; 9-(4-PHENYLBENZYL)-2,3-DIHYDROIMIDAZO(1,2-A)BENZIMIDAZOLE; ANTIPARASITIC AGENT; FUSED HETEROCYCLIC RINGS;

EID: 84904557798     PISSN: 02235234     EISSN: 17683254     Source Type: Journal    
DOI: 10.1016/j.ejmech.2014.07.038     Document Type: Article
Times cited : (47)

References (29)
  • 2
    • 33846205114 scopus 로고    scopus 로고
    • Molecular diagnosis of leishmaniasis: Current status and future applications
    • DOI 10.1128/JCM.02029-06
    • R. Reithinger, and J.C. Dujardin Molecular diagnosis of leishmaniasis: current status and future applications J. Clin. Microbiol. 45 2007 21 25 (Pubitemid 46106401)
    • (2007) Journal of Clinical Microbiology , vol.45 , Issue.1 , pp. 21-25
    • Reithinger, R.1    Dujardin, J.-C.2
  • 3
    • 0027960239 scopus 로고
    • Visceral leishmaniasis: More prevalent and more problematic
    • DOI 10.1016/S0163-4453(94)91059-6
    • G.G. Baily, and A. Nandy Visceral leishmaniasis: more prevalent and more problematic J. Infect. 29 1994 241 247 (Pubitemid 24365179)
    • (1994) Journal of Infection , vol.29 , Issue.3 , pp. 241-247
    • Baily, G.G.1    Nandy, A.2
  • 5
    • 0142258171 scopus 로고    scopus 로고
    • Leishmaniasis - Current chemotherapy and recent advances in the search for novel drugs
    • DOI 10.1016/j.pt.2003.09.008
    • S.L. Croft, and G.H. Coombs Leishmaniasis - current chemotherapy and recent advances in the search for novel drugs Trends Parasitol. 19 2003 502 508 (Pubitemid 37329659)
    • (2003) Trends in Parasitology , vol.19 , Issue.11 , pp. 502-508
    • Croft, S.L.1    Coombs, G.H.2
  • 7
    • 0041767590 scopus 로고    scopus 로고
    • Leishmania donovani resistance to miltefosine involves a defective inward translocation of the drug
    • DOI 10.1128/AAC.47.8.2397-2403.2003
    • F.J. Pérez-Victoria, S. Castanys, and F. Gamarro Leishmania donovani resistance to miltefosine involves a defective inward translocation of the drug Antimicrob. Agents Chemother. 47 2003 2397 2403 (Pubitemid 36919436)
    • (2003) Antimicrobial Agents and Chemotherapy , vol.47 , Issue.8 , pp. 2397-2403
    • Perez-Victoria, F.J.1    Castanys, S.2    Gamarro, F.3
  • 9
    • 84934442209 scopus 로고    scopus 로고
    • DNA topoisomerases of Leishmania: The potential targets for anti-leishmanial therapy
    • B.B. Das, A. Ganguly, and H.K. Majumder DNA topoisomerases of Leishmania: the potential targets for anti-leishmanial therapy Adv. Exp. Med. Biol. 625 2008 103 115
    • (2008) Adv. Exp. Med. Biol. , vol.625 , pp. 103-115
    • Das, B.B.1    Ganguly, A.2    Majumder, H.K.3
  • 10
    • 44349118534 scopus 로고    scopus 로고
    • Kinetoplast as a potential chemotherapeutic target of trypanosomatids
    • DOI 10.2174/138161208784041051
    • M.C. Motta Kinetoplast as a potential chemotherapeutic target of trypanosomatids Curr. Pharm. Des. 14 2008 847 854 (Pubitemid 351736417)
    • (2008) Current Pharmaceutical Design , vol.14 , Issue.9 , pp. 847-854
    • Motta, M.C.M.1
  • 11
    • 0037846500 scopus 로고    scopus 로고
    • The parasite-specific trypanothione metabolism of trypanosoma and leishmania
    • DOI 10.1515/BC.2003.062
    • R.L. Krauth-Siegel, S.K. Meiering, and H. Schmidt The parasite-specific trypanothione metabolism of Trypanosoma and Leishmania Biol. Chem. 384 2003 539 549 (Pubitemid 36609170)
    • (2003) Biological Chemistry , vol.384 , Issue.4 , pp. 539-549
    • Krauth-Siegel, R.L.1    Meiering, S.K.2    Schmidt, H.3
  • 12
    • 0037327813 scopus 로고    scopus 로고
    • Fatty acid and sterol metabolism: Potential antimicrobial targets in apicomplexan and trypanosomatid parasitic protozoa
    • DOI 10.1016/S0166-6851(02)00280-3, PII S0166685102002803
    • C.W. Roberts, R. McLeord, D.W. Rice, M. Ginger, M.L. Chance, and L.J. Goad Fatty acid and sterol metabolism: potential antimicrobial targets in apicomplexan and trypanosomatid parasitic protozoa Mol. Biochem. Parasitol. 126 2003 129 142 (Pubitemid 36255612)
    • (2003) Molecular and Biochemical Parasitology , vol.126 , Issue.2 , pp. 129-142
    • Roberts, C.W.1    McLeod, R.2    Rice, D.W.3    Ginger, M.4    Chance, M.L.5    Goad, L.J.6
  • 13
    • 72249097281 scopus 로고    scopus 로고
    • Neglected tropical diseases: Multi-target-directed ligands in the search for novel lead candidates against Trypanosoma and Leishmania
    • A. Cavalli, and M.L. Bolognesi Neglected tropical diseases: multi-target-directed ligands in the search for novel lead candidates against Trypanosoma and Leishmania J. Med. Chem. 52 2009 7339 7359
    • (2009) J. Med. Chem. , vol.52 , pp. 7339-7359
    • Cavalli, A.1    Bolognesi, M.L.2
  • 14
    • 12144263088 scopus 로고    scopus 로고
    • The effect of topoisomerase II inhibitors on the kinetoplast ultrastructure
    • DOI 10.1007/s00436-004-1223-4
    • D.P. Cavalcanti, S.P. Fragoso, S. Goldenberg, W. de Souza, and M.C. Motta The effect of topoisomerase II inhibitors on the kinetoplast ultrastructure Parasitol. Res. 94 2004 439 448 (Pubitemid 40104523)
    • (2004) Parasitology Research , vol.94 , Issue.6 , pp. 439-448
    • Cavalcanti, D.P.1    Fragoso, S.P.2    Goldenberg, S.3    De Souza, W.4    Motta, M.C.M.5
  • 18
    • 33751080094 scopus 로고    scopus 로고
    • Drug discovery and development for neglected parasitic diseases
    • DOI 10.1038/nchembio837, PII NCHEMBIO837
    • A.R. Renslo, and J.H. McKerrow Drug discovery and development for neglected parasitic diseases Nat. Chem. Biol. 2 2006 701 710 (Pubitemid 44764212)
    • (2006) Nature Chemical Biology , vol.2 , Issue.12 , pp. 701-710
    • Renslo, A.R.1    McKerrow, J.H.2
  • 19
    • 26844461073 scopus 로고    scopus 로고
    • Chemotherapy of trypanosomiases and leishmaniasis
    • DOI 10.1016/j.pt.2005.08.026, PII S1471492205002539
    • S.L. Croft, M.P. Barrett, and J.A. Urbina Chemotherapy of trypanosomiases and leishmaniasis Trends Parasitol. 21 2005 508 512 (Pubitemid 41447021)
    • (2005) Trends in Parasitology , vol.21 , Issue.11 , pp. 508-512
    • Croft, S.L.1    Barrett, M.P.2    Urbina, J.A.3
  • 22
    • 0024643456 scopus 로고
    • Syntheses of the metabolites of 2-ethoxyethyl)-2-(hexahydro-4-methyl-1H- 1,4-diazepin-1-yl)-1H-benzimidazole difumarate (KG-2413) and related compounds
    • R. Iemura, M. Hori, and H. Ohtaka Syntheses of the metabolites of 1-(2-ethoxyehtyl)-2-(hexahydro-4-methyl-1 H-1,4-diazepin-1-yl)-1H-benzimidazole difumarate (KG-2413) and related compounds Chem. Pharm. Bull. 37 1989 962 966 (Pubitemid 19144136)
    • (1989) Chemical and Pharmaceutical Bulletin , vol.37 , Issue.4 , pp. 962-966
    • Iemura, R.1    Hori, M.2    Ohtaka, H.3
  • 24
    • 33750910031 scopus 로고    scopus 로고
    • Synthesis and biological activity of N-acylmethyl derivatives of 9H-2,3-dihydroimidazo- and 10H-2,3,4,10-tetrahydropyrimido[1,2-a]benzimidazoles and their reduction products
    • DOI 10.1007/s11094-006-0105-8
    • V.A. Anisimova, I.E. Tolpygin, A.A. Spasov, V.A. Kosolapov, A.V. Stepanov, and A.F. Kucheryavenko Synthesis and biological activity of N-acylmethyl derivatives of 9H-2,3-dihydroimidazo- and 10H-2,3,4,10- tetrahydropyrimido[1,2-a]benzimidazoles and their reduction products Pharm. Chem. J. 40 2006 261 267 (Pubitemid 44724889)
    • (2006) Pharmaceutical Chemistry Journal , vol.40 , Issue.5 , pp. 261-267
    • Anisimova, V.A.1    Tolpygin, I.E.2    Spasov, A.A.3    Kosolapov, V.A.4    Stepanov, A.V.5    Kucheryavenko, A.F.6
  • 25
    • 77952366295 scopus 로고    scopus 로고
    • Research in the field of imidazo[1,2-a]benzimidazole derivatives: XXVII. 1-Acylmethyl-2-(ω-hydroxyalkylamino)benzimidazoles and their transformation into derivatives of tricyclic systems
    • V.A. Anisimova, I.E. Tolpygin, and G.S. Borodkin Research in the field of imidazo[1,2-a]benzimidazole derivatives: XXVII. 1-Acylmethyl-2-(ω- hydroxyalkylamino)benzimidazoles and their transformation into derivatives of tricyclic systems Russ. J. Org. Chem. 46 2010 275 285
    • (2010) Russ. J. Org. Chem. , vol.46 , pp. 275-285
    • Anisimova, V.A.1    Tolpygin, I.E.2    Borodkin, G.S.3
  • 26
    • 0029861640 scopus 로고    scopus 로고
    • Efficient technique for screening drugs for activity against Trypanosoma cruzi using parasites expressing β-galactosidase
    • F.S. Buckner, C.L. Verlinde, A.C. La Flamme, and W.C. Van Voorhis Efficient technique for screening drug for activity against Trypanosoma cruzi using parasites expressing β-galactosidase Antimicrob. Agents Chemother. 40 1996 2592 2597 (Pubitemid 26367650)
    • (1996) Antimicrobial Agents and Chemotherapy , vol.40 , Issue.11 , pp. 2592-2597
    • Buckner, F.S.1    Verlinde, C.L.M.J.2    La Flamme, A.C.3    Van Voorhis, W.C.4
  • 27
    • 84895199058 scopus 로고    scopus 로고
    • An image-based algorithm for precise and accurate high throughput assessment of drug activity against the human parasite Trypanosoma cruzi
    • S. Moon, J.L. Siqueira-Neto, C.B. Moraes, G. Yang, M. Kang, L.H. Freitas-Junior, and M.A.E. Hansen An image-based algorithm for precise and accurate high throughput assessment of drug activity against the human parasite Trypanosoma cruzi PLoS One 9 2014 e87188
    • (2014) PLoS One , vol.9 , pp. 87188
    • Moon, S.1    Siqueira-Neto, J.L.2    Moraes, C.B.3    Yang, G.4    Kang, M.5    Freitas-Junior, L.H.6    Hansen, M.A.E.7
  • 29
    • 0033003760 scopus 로고    scopus 로고
    • A simple statistical parameter for use in evaluation and validation of high throughput screening assays
    • DOI 10.1177/108705719900400206
    • J.H. Zhang, T.D. Chung, and K.R. Oldenburg A simple statistical parameter for use in evaluation and validation of high throughput screening assays J. Biomol. Screen 4 1999 67 73 (Pubitemid 29278954)
    • (1999) Journal of Biomolecular Screening , vol.4 , Issue.2 , pp. 67-73
    • Zhang, J.-H.1    Chung, T.D.Y.2    Oldenburg, K.R.3


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