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Volumn 33, Issue 4, 2010, Pages 499-502

Two new hetero-spirocyclic γ -lactam derivatives from marine sediment-derived fungus aspergillus sydowi D2-6

Author keywords

Aspergillus sydowi D2 6; Azaspirofurans A; Cytotoxicity; Marine sediment derived

Indexed keywords

3 (4,5 DIMETHYL 2 THIAZOLYL) 2,5 DIPHENYLTETRAZOLIUM BROMIDE; AZASPIROFURANS A; AZASPIROFURANS B; GAMMA LACTAM DERIVATIVE; UNCLASSIFIED DRUG;

EID: 77954523414     PISSN: 02536269     EISSN: 19763786     Source Type: Journal    
DOI: 10.1007/s12272-010-0401-4     Document Type: Article
Times cited : (42)

References (6)
  • 2
    • 0000879865 scopus 로고    scopus 로고
    • Azaspirene a novel angiogenesis inhibitor containing a 1-oxa-7-azaspiro [4,4] non-2-ene-4,6-dione skeleton produced by the fungus Neosartorya sp.
    • Asami, Y., Kakeya, H., Onose, R., Yoshida, A., Matsuzaki,H., and Osada, H., Azaspirene, a novel angiogenesis inhibitor containing a 1-oxa-7-azaspiro [4, 4] non-2-ene-4,6-dione skeleton produced by the fungus Neosartorya sp.Org. Lett., 4 , 2845-2848 (2002).
    • (2002) Org. Lett. , vol.4 , pp. 2845-2848
    • Asami, Y.1    Kakeya, H.2    Onose, R.3    Yoshida, A.4    Matsuzaki, H.5    Osada, H.6
  • 3
    • 84985088177 scopus 로고
    • Isolation and structure of pseurotin A, a microbial metabolite of Pseudeurotium ovalis STOLK with an unusual heterospirocyclic system
    • Bloch, P. and Tamm, C., Isolation and structure of pseurotin A, a microbial metabolite of Pseudeurotium ovalis STOLK with an unusual heterospirocyclic system. Helv. Chim.Acta, 64, 304-315 (1981).
    • (1981) Helv. Chim.Acta , vol.64 , pp. 304-315
    • Bloch, P.1    Tamm, C.2
  • 4
    • 36349008637 scopus 로고    scopus 로고
    • Pinpointing pseurotins from a marine-derived Aspergillus as tools for chemical genetics using a synthetic lethality yeast screen
    • Boot, C., Gassner, N. C., Compton, J. E., Tenney, K.,Tamble, C. M., Lokey, R. S., Holman, T. R., and Crews, P.,Pinpointing pseurotins from a marine-derived Aspergillus as tools for chemical genetics using a synthetic lethality yeast screen. J. Nat. Prod., 70, 1672-1675 (2007).
    • (2007) J. Nat. Prod. , vol.70 , pp. 1672-1675
    • Boot, C.1    Gassner, N.C.2    Compton, J.E.3    Tenney, K.4    Tamble, C.M.5    Lokey, R.S.6    Holman, T.R.7    Crews, P.8
  • 5
    • 22144441375 scopus 로고    scopus 로고
    • First asymmetric total synthesis of synerazol an antifungal antibiotic, and determination of its absolute stereochemistry
    • Hayashi, Y., Shoji, M., Mukaiyama, T., Gotoh, H., Yamaguchi,S., Nakata, H., and Osada, H., First asymmetric total synthesis of synerazol, an antifungal antibiotic, and determination of its absolute stereochemistry. J. Org. Lett., 70,5643-5654 (2005).
    • (2005) J. Org. Lett. , vol.70 , pp. 5643-5654
    • Hayashi, Y.1    Shoji, M.2    Mukaiyama, T.3    Gotoh, H.YamaguchiS.4    Nakata, H.5    Osada, H.6
  • 6
    • 0021061819 scopus 로고
    • Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assay
    • Mossman, T., Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assay. J. Immunol. Methods, 65, 55-63 (1983).
    • (1983) J. Immunol. Methods , vol.65 , pp. 55-63
    • Mossman, T.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.