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Volumn 9, Issue 1, 2010, Pages 1-12

Natural products with translocase I inhibitory activity, as new lead compounds against tuberculosis;Produtos naturais com atividade inibitória da translocase I, uma promissora classe de compostos contra tuberculose

Author keywords

Streptomyces; Translocase I; Tuberculosis

Indexed keywords

A 500359A; A 500359E; CALANOLIDE A; CAPRAZAMICINE DERIVATIVE; CAPRAZOL; CAPURAMICINA; CAPURAMICINE DERIVATIVE; CARRIER PROTEIN; ENZYME INHIBITOR; ETHAMBUTOL; ISONIAZID; LIPOSIDOMICINA I; LIPOSIDOMICINA II; LIPOSIDOMICINA III; LIPOSIDOMICINA IV; LIPOSIDOMICINE DERIVATIVE; MURAIMICINE DERIVATIVE; MUREIDOMICINE DERIVATIVE; NAPSAMICINE DERIVATIVE; NATURAL PRODUCT; PACIDAMICINE DERIVATIVE; PALMITOILCAPRAZOL; PEPTIDOGLYCAN; PYRAZINAMIDE; RIFAMPICIN; RS 124922; TRANSLOCASE I; TUBERCULOSTATIC AGENT; TUNICAMICINE DERIVATIVE; UNCLASSIFIED DRUG; UNINDEXED DRUG;

EID: 76749171748     PISSN: None     EISSN: 07177917     Source Type: Journal    
DOI: None     Document Type: Review
Times cited : (4)

References (43)
  • 3
    • 0031725647 scopus 로고    scopus 로고
    • mraY is an essential gene for cell growth in Echeriachia Coli
    • Boyle DS, Donachie WD. 1998. mraY is an essential gene for cell growth in Echeriachia Coli. J. Bacteriol. 180(23) 6429-6432.
    • (1998) J. Bacteriol , vol.180 , Issue.23 , pp. 6429-6432
    • Boyle, D.S.1    Donachie, W.D.2
  • 4
    • 0026880575 scopus 로고
    • Intracellular steps of bacterial cell wall peptidoglycan biosynthesis: Enzymology, antibiotics and antibiotic resistance
    • Bugg TDH, Walsh, CT. 1992. Intracellular steps of bacterial cell wall peptidoglycan biosynthesis: Enzymology, antibiotics and antibiotic resistance. Nat. Prod. Rep. 9: 199-215.
    • (1992) Nat. Prod. Rep , vol.9 , pp. 199-215
    • Bugg, T.D.H.1    Walsh, C.T.2
  • 5
    • 76749150576 scopus 로고    scopus 로고
    • Centers For Disease Control And Prevention. Extensively Drug-Resistant Tuberculosis (XDR TB). http://www.cdc.gov/tb/xdrtb/ (consulted June 29, 2009)
    • Centers For Disease Control And Prevention. Extensively Drug-Resistant Tuberculosis (XDR TB). http://www.cdc.gov/tb/xdrtb/ (consulted June 29, 2009)
  • 7
    • 0024593455 scopus 로고
    • Pacidamycins, a novel series of antibiotics with anti-pseudomonas aeruginosa activity. II. Isolation and structural elucidation
    • Chen R H, Buko AM, Whittern DN, Mcalpine JB. 1989. Pacidamycins, a novel series of antibiotics with anti-pseudomonas aeruginosa activity. II. Isolation and structural elucidation. J. Antibiot. 42(4): 512-520.
    • (1989) J. Antibiot , vol.42 , Issue.4 , pp. 512-520
    • Chen, R.H.1    Buko, A.M.2    Whittern, D.N.3    Mcalpine, J.B.4
  • 8
    • 0038674587 scopus 로고    scopus 로고
    • Antimycobacterial Activity of Phorbol Esters from the Fruits of Sapium indicum
    • Chumkaew P, Karalai C, Ponglimanont C, Chantrapromma K. 2003. Antimycobacterial Activity of Phorbol Esters from the Fruits of Sapium indicum J. Nat. Prod. 66: 540-543.
    • (2003) J. Nat. Prod , vol.66 , pp. 540-543
    • Chumkaew, P.1    Karalai, C.2    Ponglimanont, C.3    Chantrapromma, K.4
  • 9
    • 23744511266 scopus 로고    scopus 로고
    • Fármacos no combate à tuberculose: Passado, presente e futuro.
    • De Souza MVN, Vasconcelos TRA. 2005a. Fármacos no combate à tuberculose: passado, presente e futuro. Quím. Nova. 28(4): 678-682.
    • (2005) Quím. Nova , vol.28 , Issue.4 , pp. 678-682
    • De Souza, M.V.N.1    Vasconcelos, T.R.A.2
  • 10
    • 33644923867 scopus 로고    scopus 로고
    • Plants and fungal products with activity against tuberculosis
    • De Souza MV. 2005b. Plants and fungal products with activity against tuberculosis. ScientificWorldJournal. 5:609-28.
    • (2005) ScientificWorldJournal , vol.5 , pp. 609-628
    • De Souza, M.V.1
  • 11
    • 76749098204 scopus 로고    scopus 로고
    • Tuberculose em pacientes HIV-positivos: Um grave problema de saúde pública mundial.
    • De Souza MVN. 2006a. Tuberculose em pacientes HIV-positivos: um grave problema de saúde pública mundial. Rev. Bras. Farm. 87: 42-44.
    • (2006) Rev. Bras. Farm , vol.87 , pp. 42-44
    • De Souza, M.V.N.1
  • 12
    • 33745039776 scopus 로고    scopus 로고
    • Current status and future prospects for new therapies for pulmonary tuberculosis
    • De Souza MVN. 2006b. Current status and future prospects for new therapies for pulmonary tuberculosis. Curr. Opin. Pulm. Med. 12(3): 167-171.
    • (2006) Curr. Opin. Pulm. Med , vol.12 , Issue.3 , pp. 167-171
    • De Souza, M.V.N.1
  • 13
    • 33746754139 scopus 로고    scopus 로고
    • Marine natural products against tuberculosis
    • De Souza MVN. 2006d. Marine natural products against tuberculosis. ScientificWorldJournal. 6:847-861.
    • (2006) ScientificWorldJournal , vol.6 , pp. 847-861
    • De Souza, M.V.N.1
  • 15
    • 70349823195 scopus 로고    scopus 로고
    • De Souza MVN. 2009. Promising candidates in clinical trials against multidrug-resistant tuberculosis (MDR-TB) based on natural products. Fitoterapia. Edizione Farmaceutica. 80: 453-460.
    • De Souza MVN. 2009. Promising candidates in clinical trials against multidrug-resistant tuberculosis (MDR-TB) based on natural products. Fitoterapia. Edizione Farmaceutica. 80: 453-460.
  • 16
    • 0034698781 scopus 로고    scopus 로고
    • Synthesis of the nucleoside moiety of liposidomycins: Elucidation of the pharmacophore of this family of MraY inhibitors
    • Dini C, Collette P, Drochon N, Guillot JC, Lemoine G, Mauvais P, Aszodi J. 2000. Synthesis of the nucleoside moiety of liposidomycins: elucidation of the pharmacophore of this family of MraY inhibitors. Bioorg. Med. Chem. Lett. 10: 1839-1843.
    • (2000) Bioorg. Med. Chem. Lett , vol.10 , pp. 1839-1843
    • Dini, C.1    Collette, P.2    Drochon, N.3    Guillot, J.C.4    Lemoine, G.5    Mauvais, P.6    Aszodi, J.7
  • 17
    • 0035952253 scopus 로고    scopus 로고
    • Synthesis of analogues of the O-β-D-ribofuranosyl nucleoside moiety of liposidomicyns. Part 1: Contribution of the amino group and the uracil moiety upon the inhibition of MraY
    • Dini C, Drochon N, Feteanu S, Guillot JC, Peixoto C, Aszodi J. 2001a. Synthesis of analogues of the O-β-D-ribofuranosyl nucleoside moiety of liposidomicyns. Part 1: contribution of the amino group and the uracil moiety upon the inhibition of MraY. Bioorg. Med. Chem. Lett. 11: 529-531.
    • (2001) Bioorg. Med. Chem. Lett , vol.11 , pp. 529-531
    • Dini, C.1    Drochon, N.2    Feteanu, S.3    Guillot, J.C.4    Peixoto, C.5    Aszodi, J.6
  • 18
    • 0035952292 scopus 로고    scopus 로고
    • Synthesis of analogues of the O-β-D-ribofuranosyl nucleoside moiety of liposidomicyns. Part 2: Role of the hydroxyl groups upon the inhibition of MraY
    • Dini C, Drochon N, Guillot JC, Mauvais P, Walter P, Aszodi J. 2001b. Synthesis of analogues of the O-β-D-ribofuranosyl nucleoside moiety of liposidomicyns. Part 2: role of the hydroxyl groups upon the inhibition of MraY. Bioorg. Med. Chem. Lett. 11: 533-536.
    • (2001) Bioorg. Med. Chem. Lett , vol.11 , pp. 533-536
    • Dini, C.1    Drochon, N.2    Guillot, J.C.3    Mauvais, P.4    Walter, P.5    Aszodi, J.6
  • 19
    • 0024509967 scopus 로고
    • Pacidamycins, a novel series of antibiotics with anti-Pseudomonas aeruginosa activity. III. Microbiologic profile
    • Fernandes P B, Swanson R N, Hardy D J, Hanson C W, Coen L, Rasmussen R R, Chen R H. 1989. Pacidamycins, a novel series of antibiotics with anti-Pseudomonas aeruginosa activity. III. Microbiologic profile. J. antibiotic. XLII (4). 521-526.
    • (1989) J. antibiotic , vol.42 , Issue.4 , pp. 521-526
    • Fernandes, P.B.1    Swanson, R.N.2    Hardy, D.J.3    Hanson, C.W.4    Coen, L.5    Rasmussen, R.R.6    Chen, R.H.7
  • 20
    • 0034762821 scopus 로고    scopus 로고
    • Recent advances in the formation of bacterial peptidoglycan monomer unit
    • Heijenoort, JV .2001. Recent advances in the formation of bacterial peptidoglycan monomer unit. Nat. Prod. Rep. 18:503-519.
    • (2001) Nat. Prod. Rep , vol.18 , pp. 503-519
    • Heijenoort, J.V.1
  • 21
    • 0014480822 scopus 로고
    • Initial state in peptidoglycan synthesis. III. Kinetics and uncoupling of phospho-N-acetylmuramylpentapeptide translocase (uridine 5′-phosphate)
    • Heydanek MG, Struve WG, Neuhaus FC. 1969. Initial state in peptidoglycan synthesis. III. Kinetics and uncoupling of phospho-N-acetylmuramylpentapeptide translocase (uridine 5′-phosphate). Biochem. 63(8): 1214-1221.
    • (1969) Biochem , vol.63 , Issue.8 , pp. 1214-1221
    • Heydanek, M.G.1    Struve, W.G.2    Neuhaus, F.C.3
  • 22
    • 40949120496 scopus 로고    scopus 로고
    • Synthesis of caprazamycin analogues and their structure activity relationship for antibacterial activity
    • Hirano S, Ichikawa S, Matsuda A. 2008a. Synthesis of caprazamycin analogues and their structure activity relationship for antibacterial activity. J. Org. Chem. 73(2): 569-577.
    • (2008) J. Org. Chem , vol.73 , Issue.2 , pp. 569-577
    • Hirano, S.1    Ichikawa, S.2    Matsuda, A.3
  • 23
    • 43049148337 scopus 로고    scopus 로고
    • Structure-activity relationship of truncated analogs of caprazamycins as potential anti-tuberculosis agents
    • Hirano S, Ichikawa S, Matsuda A. 2008b. Structure-activity relationship of truncated analogs of caprazamycins as potential anti-tuberculosis agents. Bioorg. Med. Chem. 16: 5123-5133.
    • (2008) Bioorg. Med. Chem , vol.16 , pp. 5123-5133
    • Hirano, S.1    Ichikawa, S.2    Matsuda, A.3
  • 26
    • 48849113332 scopus 로고    scopus 로고
    • Nucleoside chemistry based on nucleoside natural products synthesis
    • Ichikawa S. 2008. Nucleoside chemistry based on nucleoside natural products synthesis. Chem Pharm. Bull. 56(8): 1059-1072.
    • (2008) Chem Pharm. Bull , vol.56 , Issue.8 , pp. 1059-1072
    • Ichikawa, S.1
  • 27
    • 34248392226 scopus 로고    scopus 로고
    • Nucleoside natural products and related analogs with potential therapeutic properties as antibacterial and antiviral agents
    • Ichikawa S, Matsuda A. 2007. Nucleoside natural products and related analogs with potential therapeutic properties as antibacterial and antiviral agents. Expert Opin. Ther. Pat. 17(5): 487-498.
    • (2007) Expert Opin. Ther. Pat , vol.17 , Issue.5 , pp. 487-498
    • Ichikawa, S.1    Matsuda, A.2
  • 29
    • 0027233035 scopus 로고
    • Selective inhibition of the bacterial translocasereaction in peptidoglycan synthesis by mureidomycins
    • Inukai M, Isono F, Takatsuki A. 1993. Selective inhibition of the bacterial translocasereaction in peptidoglycan synthesis by mureidomycins. Antimicrob. Agents Chemother.37(5): 980-983.
    • (1993) Antimicrob. Agents Chemother , vol.37 , Issue.5 , pp. 980-983
    • Inukai, M.1    Isono, F.2    Takatsuki, A.3
  • 31
    • 0026772903 scopus 로고
    • Susceptibily of Pseudomonas species to the novel antibiotics mureidomycins
    • Isono F, Kodoma K, Inukai M. 1992. Susceptibily of Pseudomonas species to the novel antibiotics mureidomycins. Antimicob. Agents Chemother. 36(5): 1024-1027.
    • (1992) Antimicob. Agents Chemother , vol.36 , Issue.5 , pp. 1024-1027
    • Isono, F.1    Kodoma, K.2    Inukai, M.3
  • 32
    • 14544280700 scopus 로고    scopus 로고
    • New Bioactive Clerodane Diterpenoids from the Bark of Casearia grewiifolia
    • Kanokmedhakul S, Kanokmedhakul K, Kanarsa T, Buayairaksa. 2005. New Bioactive Clerodane Diterpenoids from the Bark of Casearia grewiifolia. J. Nat. Prod. 68: 183-188.
    • (2005) J. Nat. Prod , vol.68 , pp. 183-188
    • Kanokmedhakul, S.1    Kanokmedhakul, K.2    Kanarsa, T.3    Buayairaksa4
  • 33
    • 3042536582 scopus 로고    scopus 로고
    • New Bioactive Prenylflavonoids and Dibenzocycloheptene Derivative from Roots of Dendrolobium lanceolatum
    • Kanokmedhakul, S, Kanokmedhakul K, Nambuddee K, Kongsaeree P. 2004. New Bioactive Prenylflavonoids and Dibenzocycloheptene Derivative from Roots of Dendrolobium lanceolatum. J. Nat. Prod. 67: 968-972.
    • (2004) J. Nat. Prod , vol.67 , pp. 968-972
    • Kanokmedhakul, S.1    Kanokmedhakul, K.2    Nambuddee, K.3    Kongsaeree, P.4
  • 34
    • 0032428375 scopus 로고    scopus 로고
    • Selective inhibition of the bacterial peptidoglycan biosynthesis by the new types of liposidomycins
    • Kimura KI, Iked Y, Kagami S, Yoshihama M, Suzuki K, Osada H, Isono K. 1998. Selective inhibition of the bacterial peptidoglycan biosynthesis by the new types of liposidomycins. J. Antibiotics. 51(12): 1099-1104.
    • (1998) J. Antibiotics , vol.51 , Issue.12 , pp. 1099-1104
    • Kimura, K.I.1    Iked, Y.2    Kagami, S.3    Yoshihama, M.4    Suzuki, K.5    Osada, H.6    Isono, K.7
  • 35
    • 0037394583 scopus 로고    scopus 로고
    • Recent advances in antimicrobial nucleoside antibiotics targeting cell wall biosynthesis
    • Kimura K, Bugg TDH. 2003. Recent advances in antimicrobial nucleoside antibiotics targeting cell wall biosynthesis. Nat. Prod. Rep. 20: 252-273.
    • (2003) Nat. Prod. Rep , vol.20 , pp. 252-273
    • Kimura, K.1    Bugg, T.D.H.2
  • 39
    • 0026458015 scopus 로고
    • Transport proteins in bacteria: Common themes in their design
    • Nikaido H, Saier JR MH. 1994. Transport proteins in bacteria: common themes in their design. Science. 258(5084): 936-942.
    • (1994) Science , vol.258 , Issue.5084 , pp. 936-942
    • Nikaido, H.1    Saier, J.M.2
  • 41
    • 0013871031 scopus 로고
    • On the initial stage in peptidoglycan synthesis. Phospho-N-acetylmuramylpentapeptide tranlocase (uridine monophosphate)
    • Struve WG, Sinha RK, Neuhaus FC. 1966. On the initial stage in peptidoglycan synthesis. Phospho-N-acetylmuramylpentapeptide tranlocase (uridine monophosphate). Biochem. 5(1): 82-93.
    • (1966) Biochem , vol.5 , Issue.1 , pp. 82-93
    • Struve, W.G.1    Sinha, R.K.2    Neuhaus, F.C.3
  • 42
    • 76749166694 scopus 로고    scopus 로고
    • World Health Organization. Tuberculosis (TB). http://www.who.int/tb/en/ (consulted June 16, 2009)
    • World Health Organization. Tuberculosis (TB). http://www.who.int/tb/en/ (consulted June 16, 2009)
  • 43
    • 1342300734 scopus 로고    scopus 로고
    • Anti-HIV natural product (+)-calanolide A is active against both drug-susceptible and drug-resistant strains of Mycobacterium tuberculosis
    • Xu ZQ, Barrow WW, Suling WJ, Westbrook L, Barrow E, Lin Y M, Flavin M .T. 2004. Anti-HIV natural product (+)-calanolide A is active against both drug-susceptible and drug-resistant strains of Mycobacterium tuberculosis. Bioorg. Med. Chem. 12: 1199-1207.
    • (2004) Bioorg. Med. Chem , vol.12 , pp. 1199-1207
    • Xu, Z.Q.1    Barrow, W.W.2    Suling, W.J.3    Westbrook, L.4    Barrow, E.5    Lin, Y.M.6    Flavin, M.T.7


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