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Volumn 46, Issue 8, 2011, Pages 3339-3347

Synthesis and evaluation of mansonone F derivatives as topoisomerase inhibitors

Author keywords

Cytotoxic activity; Mansonone F derivatives; Synthesis; Topoisomerase I; Topoisomerase II

Indexed keywords

2 (1,2 DIHYDRO 3 METHYL 1,2 DIOXY 4 NAPHTHOXY)ACETONITRILE; 3 (4 FLUOROBENZYL) 9 CHLOROBENZO[DE]BENZOPYRAN 7,8 DIONE; 3 (4 FLUOROPHENYL) 3 HYDROXYL 2,3 DIHYDROBENZO[DE]BENZOPYRAN 7,8 DIONE; 3 (4 FLUOROPHENYL) 3 HYDROXYL 9 CHLORO 2,3 DIHYDROBENZO[DE]BENZOPYRAN 7,8 DIONE; 3 (4 FLUOROPHENYL)BENZO[DE]BENZOPYRAN 7,8 DIONE; 3 ALLYL 3 HYDROXYL 9 CHLORO 2,3 DIHYDROBENZO[DE]BENZOPYRAN 7,8 DIONE; 3 ALLYL 9 CHLOROBENZO[DE]BENZOPYRAN 7,8 DIONE; 3 BENZYL 3 HYDROXYL 2,3 DIHYDROBENZO[DE]BENZOPYRAN 7,8 DIONE; 3 BENZYL 3 HYDROXYL 9 CHLORO 2,3 DIHYDROBENZO[DE]BENZOPYRAN 7,8 DIONE; 3 BENZYL 9 CHLOROBENZO[DE]BENZOPYRAN 7,8 DIONE; 3 BENZYLBENZO[DE]BENZOPYRAN 7,8 DIONE; 3 METHYL 2,3 DIHYDROBENZO[DE]BENZOPYRAN 7,8 DIONE; 3 METHYL 3 HYDROXYL 2,3 DIHYDROBENZO[DE]BENZOPYRAN 7,8 DIONE; 3 METHYL 3 HYDROXYL 9 CHLORO 2,3 DIHYDROBENZO[DE]BENZOPYRAN 7,8 DIONE; 3 N PROPYL 3 HYDROXYL 9 CHLORO 2,3 DIHYDROBENZO[DE]BENZOPYRAN 7,8 DIONE; 3 PHENYL 3 HYDROXYL 2,3 DIHYDROBENZO[DE]BENZOPYRAN 7,8 DIONE; 3 PHENYL 3 HYDROXYL 9 CHLORO 2,3 DIHYDROBENZO[DE]BENZOPYRAN 7,8 DIONE; 3 PHENYL 9 CHLOROBENZO[DE]BENZOPYRAN 7,8 DIONE; 3 PHENYLBENZO[DE]BENZOPYRAN 7,8 DIONE; 3 PROPYL 9 CHLOROBENZO[DE]BENZOPYRAN 7,8 DIONE; 4 (2 OXYPROPROXY) 3 METHYL 1,2 NAPHTHOQUINONE; 4 ALLYL 3 METHYL 1,2 NAPHTHOQUINONE; ANTINEOPLASTIC AGENT; DNA TOPOISOMERASE; DNA TOPOISOMERASE (ATP HYDROLYSING); DNA TOPOISOMERASE INHIBITOR; ETOPOSIDE; MANSONONE F DERIVATIVE; METHYL 3 BENZOYLOXY 9 CHLORO 2,3 DIHYDROBENZO[DE]BENZOPYRAN 7,8 DIONE; UNCLASSIFIED DRUG; UNINDEXED DRUG;

EID: 79958290924     PISSN: 02235234     EISSN: 17683254     Source Type: Journal    
DOI: 10.1016/j.ejmech.2011.04.059     Document Type: Article
Times cited : (42)

References (20)
  • 1
    • 0034923502 scopus 로고    scopus 로고
    • DNA topoisomerases: Structure, function, and mechanism
    • DOI 10.1146/annurev.biochem.70.1.369
    • J.J. Champoux DNA topoisomerases: structure, function, and mechanism Annu. Rev. Biochem. 70 2001 369 413 (Pubitemid 32662215)
    • (2001) Annual Review of Biochemistry , vol.70 , pp. 369-413
    • Champoux, J.J.1
  • 2
    • 77954187741 scopus 로고    scopus 로고
    • DNA topoisomerases and their poisoning by anticancer and antibacterial drugs
    • Y. Pommier, E. Leo, H. Zhang, and C. Marchand DNA topoisomerases and their poisoning by anticancer and antibacterial drugs Chem. Biol. 17 2010 421 433
    • (2010) Chem. Biol. , vol.17 , pp. 421-433
    • Pommier, Y.1    Leo, E.2    Zhang, H.3    Marchand, C.4
  • 3
    • 0002821759 scopus 로고
    • Quinonoid pigments Mansonia Altissima
    • N. Tanaka, M. Yasue, and H. Imamura Quinonoid pigments Mansonia Altissima Tetrahedron Lett. 24 1966 2767 2773
    • (1966) Tetrahedron Lett. , vol.24 , pp. 2767-2773
    • Tanaka, N.1    Yasue, M.2    Imamura, H.3
  • 9
    • 57349116976 scopus 로고    scopus 로고
    • Inhibition of thioredoxin reductase by mansonone F analogues: Implications for anticancer activity
    • Z. Liu, S.L. Huang, M.M. Li, Z.S. Huang, K.S. Lee, and L.Q. Gu Inhibition of thioredoxin reductase by mansonone F analogues: implications for anticancer activity Chem. Biol. Interact. 177 2009 48 57
    • (2009) Chem. Biol. Interact. , vol.177 , pp. 48-57
    • Liu, Z.1    Huang, S.L.2    Li, M.M.3    Huang, Z.S.4    Lee, K.S.5    Gu, L.Q.6
  • 11
    • 0034617161 scopus 로고    scopus 로고
    • Facile construction of the oxaphenalene skeleton by peri ring closure. Formal synthesis of mansonone F
    • Y.-G. Suh, D.-Y. Shin, K.-H. Min, S.-S. Hyun, J.-K. Jung, and S.-Y. Seo Facile construction of the oxaphenalene skeleton by peri ring closure. formal synthesis mansonone F Chem. Commun. 13 2000 1203 1204 (Cambridge) (Pubitemid 30435381)
    • (2000) Chemical Communications , Issue.13 , pp. 1203-1204
    • Suh, Y.-G.1    Shin, D.-Y.2    Min, K.-H.3    Hyun, S.-S.4    Jung, J.-K.5    Seo, S.-Y.6
  • 12
    • 84970572142 scopus 로고
    • Intramolecular Diels-Alder additions of benzynes to furans. Application to the total synthesis of biflorin, and the mansonones E, I, and F
    • W.M. Best, and D. Wege Intramolecular Diels-Alder additions of benzynes to furans. Application to the total synthesis of biflorin, and the mansonones E, I, and F Aust. J. Chem. 39 1986 647 666
    • (1986) Aust. J. Chem. , vol.39 , pp. 647-666
    • Best, W.M.1    Wege, D.2
  • 13
    • 51349140375 scopus 로고    scopus 로고
    • A facile synthesis of novel heteropolycyclic pyrazines and oxazoles and mechanistic studies of 2,3-dihydrobenzo[de]-chromene-7,8-dione with amines
    • H.P. Jian, X.Y. Wang, Z.S. Huang, S.L. Huang, and L.Q. Gu A facile synthesis of novel heteropolycyclic pyrazines and oxazoles and mechanistic studies of 2,3-dihydrobenzo[de]-chromene-7,8-dione with amines Heterocycles 75 2008 1773 1778
    • (2008) Heterocycles , vol.75 , pp. 1773-1778
    • Jian, H.P.1    Wang, X.Y.2    Huang, Z.S.3    Huang, S.L.4    Gu, L.Q.5
  • 14
    • 33745507940 scopus 로고    scopus 로고
    • The mechanism on cyclization, debenzylation and oxidation of 1-[1-(benzyloxy)-3-methylnaphthalen-4-yloxy]propan-2-one
    • S.L. Huang, Y. Luo, Z.S. Huang, X.Z. Bu, P.Q. Liu, L. Ma, Y.M. Li, A.S.C. Chan, and L.Q. Gu The mechanism on cyclization, debenzylation, and oxidation of 1-[1-(benzyloxy)-3-methyl- naphthalen-4-yloxy]propan-2-one Chin. Chem. Lett. 17 2006 769 772 (Pubitemid 43962433)
    • (2006) Chinese Chemical Letters , vol.17 , Issue.6 , pp. 769-772
    • Huang, S.L.1    Luo, Y.2    Huang, Z.S.3    Bu, X.Z.4    Liu, P.Q.5    Ma, L.6    Li, Y.M.7    Chan, A.S.C.8    Gu, L.Q.9
  • 15
    • 0021061819 scopus 로고
    • Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays
    • T. Mosmann Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays J. Immunol. Methods 65 1983 55 63 (Pubitemid 14203433)
    • (1983) Journal of Immunological Methods , vol.65 , Issue.1-2 , pp. 55-63
    • Mosmann, T.1
  • 16
    • 0035885187 scopus 로고    scopus 로고
    • Salvicine, a novel DNA topoisomerase II inhibitor, exerting its effects by trapping enzyme-DNA cleavage complexes
    • DOI 10.1016/S0006-2952(01)00732-8, PII S0006295201007328
    • L.H. Meng, J.S. Zhang, and J. Ding Salvicine, a novel DNA topoisomerase II inhibitor, exerting its effects by trapping enzyme-DNA cleavage complexes Biochem. Pharmacol. 62 2001 733 741 (Pubitemid 32816990)
    • (2001) Biochemical Pharmacology , vol.62 , Issue.6 , pp. 733-741
    • Meng, L.-H.1    Zhang, J.-S.2    Ding, J.3
  • 18
    • 0027377069 scopus 로고
    • -Lapachone, a novel DNA topoisomerase I inhibitor with a mode of action different from camptothecin
    • C.J. Li, L. Averboukh, and A.B. Pardee beta-Lapachone, a novel DNA topoisomerase I inhibitor with a mode of action different from camptothecin J. Biol. Chem. 268 1993 22463 22468 (Pubitemid 23318296)
    • (1993) Journal of Biological Chemistry , vol.268 , Issue.30 , pp. 22463-22468
    • Li, C.J.1    Averboukh, L.2    Pardee, A.B.3
  • 19
    • 77649234080 scopus 로고    scopus 로고
    • Telomerase activity and hepatic functions of rat embryonic liver progenitor cell in nanoscaffold-coated model bioreactor
    • S. Giri, K. Nieber, A. Acikgöz, S. Pavlica, M. Keller, and A. Bader Telomerase activity and hepatic functions of rat embryonic liver progenitor cell in nanoscaffold-coated model bioreactor Mol. Cell. Biochem. 336 2009 137 149
    • (2009) Mol. Cell. Biochem. , vol.336 , pp. 137-149
    • Giri, S.1    Nieber, K.2    Acikgöz, A.3    Pavlica, S.4    Keller, M.5    Bader, A.6


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