메뉴 건너뛰기




Volumn 62, Issue 7-8, 2007, Pages 567-570

Mollisianitrile, a new antibiotic from Mollisia sp. A59-96

Author keywords

Antimicrobial and cytotoxic activities; Mollisia; Mollisianitrile

Indexed keywords

MOLLISIA;

EID: 34548652025     PISSN: 09395075     EISSN: None     Source Type: Journal    
DOI: 10.1515/znc-2007-7-817     Document Type: Article
Times cited : (6)

References (14)
  • 1
    • 0024436412 scopus 로고
    • Assay of the biological activities of guaiane sesquiterpenoids isolated from the fruit bodies of edible Lactarius species
    • Anke H., Bergendorff O., and Sterner O. (1989), Assay of the biological activities of guaiane sesquiterpenoids isolated from the fruit bodies of edible Lactarius species. Food Chem. Toxicol. 27, 393-398.
    • (1989) Food Chem. Toxicol , vol.27 , pp. 393-398
    • Anke, H.1    Bergendorff, O.2    Sterner, O.3
  • 2
    • 0001150234 scopus 로고
    • De-O-methyldiaporthin, a phytotoxin from Drechslera siccans
    • Hallock Y. F., Clardy J., Kenfield D. S., and Strobel G. (1988), De-O-methyldiaporthin, a phytotoxin from Drechslera siccans. Phytochemistry 27, 3123-3125.
    • (1988) Phytochemistry , vol.27 , pp. 3123-3125
    • Hallock, Y.F.1    Clardy, J.2    Kenfield, D.S.3    Strobel, G.4
  • 3
    • 0035858425 scopus 로고    scopus 로고
    • Biosynthesis of diaporthin and orthosporin by Aspergillus ochraceus
    • Harris J. P. and Mantle P. G. (2001), Biosynthesis of diaporthin and orthosporin by Aspergillus ochraceus. Phytochemistry 57, 165-169.
    • (2001) Phytochemistry , vol.57 , pp. 165-169
    • Harris, J.P.1    Mantle, P.G.2
  • 4
    • 0024598536 scopus 로고
    • Naturally produced isocoumarins: Inhibitors of calmodulin-sensitive cyclic guanosine 3′,5′-monophosphate phosphodiesterase
    • Hedge V. R., Wittreich H., Patel M. G., Horan A. C., Hart R. F., Troynanovich J. J., Puar M. S., and Gullo V. P. (1989), Naturally produced isocoumarins: inhibitors of calmodulin-sensitive cyclic guanosine 3′,5′-monophosphate phosphodiesterase. J. Ind. Microbiol. 4, 209-213.
    • (1989) J. Ind. Microbiol , vol.4 , pp. 209-213
    • Hedge, V.R.1    Wittreich, H.2    Patel, M.G.3    Horan, A.C.4    Hart, R.F.5    Troynanovich, J.J.6    Puar, M.S.7    Gullo, V.P.8
  • 5
    • 0002415953 scopus 로고
    • Structure, synthesis, and stereochemistry of (+)-orthosporin, a phytotoxic metabolite of Rhynchosporium orthosporum
    • Ishihara A., Hashimoto M., Hirai T., Takeda I., Sasamura Y., Sakamura S., Sato R., and Tajimi A. (1989), Structure, synthesis, and stereochemistry of (+)-orthosporin, a phytotoxic metabolite of Rhynchosporium orthosporum. Chem. Lett. 8, 1495-1498.
    • (1989) Chem. Lett , vol.8 , pp. 1495-1498
    • Ishihara, A.1    Hashimoto, M.2    Hirai, T.3    Takeda, I.4    Sasamura, Y.5    Sakamura, S.6    Sato, R.7    Tajimi, A.8
  • 6
    • 34548606607 scopus 로고    scopus 로고
    • Kowalski T. and Kehr R. D. (1996), Fungal endophytes of living branch bases in several European tree species. In: Endophytic Fungi in Grasses and Woody Plants. Systematics, Ecology, and Evolution (Redlin S. C. and Carris L. M., eds.). APS Press, St. Paul, Minnesota, pp. 67-86.
    • Kowalski T. and Kehr R. D. (1996), Fungal endophytes of living branch bases in several European tree species. In: Endophytic Fungi in Grasses and Woody Plants. Systematics, Ecology, and Evolution (Redlin S. C. and Carris L. M., eds.). APS Press, St. Paul, Minnesota, pp. 67-86.
  • 7
    • 0029189274 scopus 로고
    • Induction of secondary metabolism by environmental pollutants: Metabolization of pyrene and formation of 6,8-dihydroxy-3-methylisocoumarine by Crinipellis stipitaria JK 364
    • Lange B., Kremer S., Sterner O., and Anke H. (1995), Induction of secondary metabolism by environmental pollutants: metabolization of pyrene and formation of 6,8-dihydroxy-3-methylisocoumarine by Crinipellis stipitaria JK 364. Z. Naturforsch. 50c, 806-812.
    • (1995) Z. Naturforsch , vol.50 c , pp. 806-812
    • Lange, B.1    Kremer, S.2    Sterner, O.3    Anke, H.4
  • 8
    • 0036253416 scopus 로고    scopus 로고
    • Antifungal metabolites with a new carbon skeleton from Keissleriella sp. YS4108, a marine fungus
    • Liu C. H., Meng J. C., Zou W. X., Huang L. L., Tang H. Q., and Tan R. X. (2002), Antifungal metabolites with a new carbon skeleton from Keissleriella sp. YS4108, a marine fungus. Planta Med. 68, 363-365.
    • (2002) Planta Med , vol.68 , pp. 363-365
    • Liu, C.H.1    Meng, J.C.2    Zou, W.X.3    Huang, L.L.4    Tang, H.Q.5    Tan, R.X.6
  • 11
    • 0028263071 scopus 로고
    • Fatty acids and other compounds with nematicidal activity from cultures of Basidiomycetes
    • Stadler M., Mayer A., Anke H., and Sterner O. (1994), Fatty acids and other compounds with nematicidal activity from cultures of Basidiomycetes. Planta Med. 60, 128-132.
    • (1994) Planta Med , vol.60 , pp. 128-132
    • Stadler, M.1    Mayer, A.2    Anke, H.3    Sterner, O.4
  • 12
    • 0031040138 scopus 로고    scopus 로고
    • Benesudon, a new antibiotic fungal metabolite from cultures of Mollisia benesuada (Tul.) Phill
    • Thines E., Arendholz W. R., Anke H., and Sterner O. (1997), Benesudon, a new antibiotic fungal metabolite from cultures of Mollisia benesuada (Tul.) Phill. J. Antibiot. 50, 13-17.
    • (1997) J. Antibiot , vol.50 , pp. 13-17
    • Thines, E.1    Arendholz, W.R.2    Anke, H.3    Sterner, O.4
  • 13
    • 84984104714 scopus 로고
    • Mollisin, a dichloronaphthoquinone derivative produced by the fungus Mollisia caesia
    • van der Kerk G. J. M. and Overeem J. C. (1957), Mollisin, a dichloronaphthoquinone derivative produced by the fungus Mollisia caesia. Rec. Trav. Chim. 76, 425-436.
    • (1957) Rec. Trav. Chim , vol.76 , pp. 425-436
    • van der Kerk, G.J.M.1    Overeem, J.C.2
  • 14
    • 0028835873 scopus 로고
    • Darlucins A and B, new isocyanide antibiotics from Sphaerellopsis filum (Darluca filum)
    • Zapf S., Hoßfeld M., Anke H., Velten R., and Steglich W. (1995), Darlucins A and B, new isocyanide antibiotics from Sphaerellopsis filum (Darluca filum). J. Antibiot. 48, 36-41.
    • (1995) J. Antibiot , vol.48 , pp. 36-41
    • Zapf, S.1    Hoßfeld, M.2    Anke, H.3    Velten, R.4    Steglich, W.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.