메뉴 건너뛰기




Volumn 63, Issue 9, 2010, Pages 571-574

Two 18-membered epothilones from Sorangium cellulosum So0157-2

Author keywords

18 membered macrolides; epothilone; Sorangium cellulosum So0157 2

Indexed keywords

ANTINEOPLASTIC AGENT; EPOTHILONE A; EPOTHILONE A9; EPOTHILONE B; EPOTHILONE DERIVATIVE; EPOTHILONE M; EPOTHILONE N; UNCLASSIFIED DRUG;

EID: 77957317889     PISSN: 00218820     EISSN: None     Source Type: Journal    
DOI: 10.1038/ja.2010.81     Document Type: Article
Times cited : (11)

References (16)
  • 1
    • 0029776766 scopus 로고    scopus 로고
    • Epothilone A and B-novel 16-membered macrolides with cytotoxic activity: Isolation, crystal structure, and conformation in solution
    • Höfle, G. et al. Epothilone A and B-novel 16-membered macrolides with cytotoxic activity: isolation, crystal structure, and conformation in solution. Angew. Chem. Intern. Ed. Engl. 35, 1567-1569 (1996).
    • (1996) Angew. Chem. Intern. Ed. Engl. , vol.35 , pp. 1567-1569
    • Höfle, G.1
  • 2
    • 0030018666 scopus 로고    scopus 로고
    • Epothilons A and B: Antifungal and cytotoxic compounds from Sorangium cellulosum (Myxobacteria). Production, physico-chemical and biological properties
    • Gerth, K., Bedorf, N., Höfle, G., Irschik, H. & Reichenbach, H. Epothilons A and B: antifungal and cytotoxic compounds from Sorangium cellulosum (Myxobacteria). Production, physico-chemical and biological properties. J. Antibiot. 49, 560-563 (1996).
    • (1996) J. Antibiot. , vol.49 , pp. 560-563
    • Gerth, K.1    Bedorf, N.2    Höfle, G.3    Irschik, H.4    Reichenbach, H.5
  • 3
    • 0029049468 scopus 로고
    • Epothilones, a new class of microtubule-stabilizing agents with a taxol-like mechanism of action
    • Bollag, D. M. et al. Epothilones, a new class of microtubule-stabilizing agents with a taxol-like mechanism of action. Cancer Res. 55, 2325-2333 (1995).
    • (1995) Cancer Res. , vol.55 , pp. 2325-2333
    • Bollag, D.M.1
  • 4
    • 33947253236 scopus 로고    scopus 로고
    • Evolutionary diversity of ketoacyl synthases in cellulolytic myxobacterium Sorangium
    • Li, Z. F. et al. Evolutionary diversity of ketoacyl synthases in cellulolytic myxobacterium Sorangium. Syst. Appl. Microbiol. 30, 189-1996 (2007).
    • (2007) Syst. Appl. Microbiol. , vol.30 , pp. 189-1996
    • Li, Z.F.1
  • 5
    • 34547654448 scopus 로고    scopus 로고
    • Mutation and a high-throughput screening method for improving the production of Epothilones of Sorangium
    • Gong, G. L. et al. Mutation and a high-throughput screening method for improving the production of Epothilones of Sorangium. J. Ind. Microbiol. Biotechnol. 34, 615-623 (2007).
    • (2007) J. Ind. Microbiol. Biotechnol. , vol.34 , pp. 615-623
    • Gong, G.L.1
  • 6
    • 70349603841 scopus 로고    scopus 로고
    • Five new epothilone metabolites from Sorangium cellulosum strain So0157-2
    • Wang, J. et al. Five new epothilone metabolites from Sorangium cellulosum strain So0157-2. J. Antibiot. 62, 483-487 (2009).
    • (2009) J. Antibiot. , vol.62 , pp. 483-487
    • Wang, J.1
  • 7
    • 0038352074 scopus 로고    scopus 로고
    • 16S-23S ribosomal DNA intergenic spacer regions in cellulolytic myxobacteria and differentiation of closely related strains
    • Nguimbi, E. et al. 16S-23S ribosomal DNA intergenic spacer regions in cellulolytic myxobacteria and differentiation of closely related strains. Syst. Appl. Microbiol. 26, 262-268 (2003).
    • (2003) Syst. Appl. Microbiol. , vol.26 , pp. 262-268
    • Nguimbi, E.1
  • 8
    • 0034903353 scopus 로고    scopus 로고
    • New natural epothilones from Sorangium cellulosum, strains So ce90/B2 and So ce90/D13: Isolation, structure elucidation, and SAR studies
    • Hardt, I. H. et al. New natural epothilones from Sorangium cellulosum, strains So ce90/B2 and So ce90/D13: isolation, structure elucidation, and SAR studies. J. Nat. Prod. 64, 847-856 (2001).
    • (2001) J. Nat. Prod. , vol.64 , pp. 847-856
    • Hardt, I.H.1
  • 9
    • 14844338576 scopus 로고    scopus 로고
    • Much anticipated - The bioactive conformation of epothilone and its binding to tubulin
    • Heinz, D. W., Schubert, W. & Höfle, G. Much anticipated-the bioactive conformation of epothilone and its binding to tubulin. Angew. Chem. Int. Ed. 44, 1298-1301 (2005).
    • (2005) Angew. Chem. Int. Ed. , vol.44 , pp. 1298-1301
    • Heinz, D.W.1    Schubert, W.2    Höfle, G.3
  • 10
    • 33751204460 scopus 로고    scopus 로고
    • The tubulin-bound conformation of discodermolide derived by NMR studies in solution supports a common pharmacophore model for epothilone and discodermolide13
    • Sánchez-Pedregal, V. M. et al. The tubulin-bound conformation of discodermolide derived by NMR studies in solution supports a common pharmacophore model for epothilone and discodermolide13. Angew. Chem. Int. Ed. 45, 7388-7394 (2006).
    • (2006) Angew. Chem. Int. Ed. , vol.45 , pp. 7388-7394
    • Sánchez-Pedregal, V.M.1
  • 11
    • 66349104251 scopus 로고    scopus 로고
    • Microbial transformation of epothilone A by Aspergillus niger AS 3.739
    • Wang, Y.-L. et al. Microbial transformation of epothilone A by Aspergillus niger AS 3.739. J. Asian Nat. Prod. Res. 11, 357-364 (2009).
    • (2009) J. Asian Nat. Prod. Res. , vol.11 , pp. 357-364
    • Wang, Y.-L.1
  • 12
    • 0021061819 scopus 로고
    • Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays
    • Mosmann, T. Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays. J. Immunol. Methods 65, 55-63 (1983).
    • (1983) J. Immunol. Methods , vol.65 , pp. 55-63
    • Mosmann, T.1
  • 13
    • 0032213635 scopus 로고    scopus 로고
    • Derivatization of the C12-C13 functional groups of epothilones A, B and C
    • Sefkow, M., Kiffe, M. & Höfle, G. Derivatization of the C12-C13 functional groups of epothilones A, B and C. Bioorg. Med. Chem. Lett. 8, 3031-3036 (1998).
    • (1998) Bioorg. Med. Chem. Lett. , vol.8 , pp. 3031-3036
    • Sefkow, M.1    Kiffe, M.2    Höfle, G.3
  • 14
    • 0142250006 scopus 로고    scopus 로고
    • Isolation and characterization of new epothilone analogues from recombinant Myxococcus xanthus fermentations
    • Starks, C. M., Zhou, Y., Liu, F. & Licari, P. J. Isolation and characterization of new epothilone analogues from recombinant Myxococcus xanthus fermentations. J. Nat. Prod. 66, 1313-1317 (2003).
    • (2003) J. Nat. Prod. , vol.66 , pp. 1313-1317
    • Starks, C.M.1    Zhou, Y.2    Liu, F.3    Licari, P.J.4
  • 15
    • 0036239554 scopus 로고    scopus 로고
    • Large-scale isolation and crystallization of epothilone D from Myxococcus xanthus cultures
    • Arslanian, R. L. et al. Large-scale isolation and crystallization of epothilone D from Myxococcus xanthus cultures. J. Nat. Prod. 65, 570-572 (2002).
    • (2002) J. Nat. Prod. , vol.65 , pp. 570-572
    • Arslanian, R.L.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.