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Volumn 10, Issue 19, 2008, Pages 4307-4309

Taumycins a and B, Two bioactive lipodepsipeptides from the Madagascar sponge Fascaplysinopsis sp

Author keywords

[No Author keywords available]

Indexed keywords

DEPSIPEPTIDE; PEPTIDE; TAUMYCIN A; TAUMYCIN B;

EID: 55449094954     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol801750y     Document Type: Article
Times cited : (43)

References (13)
  • 3
    • 61349108224 scopus 로고    scopus 로고
    • Taumycin A: bright orange oil, becoming greenish with acid;, α]21D 39 (c 0.23, CHCl3, IR (CHCl3) vmax 3054, 2985, 1684, 1421, 1272 cm-1; UV (MeOH) affords two absorptions at 214 and 247 nm. 1H and 13C NMR see Table 1; HRCIMS mlz 558.3559 [M, H, calcd for C31H48N3O6 558.3543, FABMS m/z 558.4 [M, H, 100
    • + (100).
  • 5
    • 61349120862 scopus 로고    scopus 로고
    • Hiemstra, H.; Houwing, H. A.; Possel, O.; Van Leusen, A. M. Can. J. Chem. 1979, 57, 3168-3170, The values for 4-subsituted oxazoles, on the other hand, are 210 and 230 Hz for CH(14) and CH(19), respectively.
    • Hiemstra, H.; Houwing, H. A.; Possel, O.; Van Leusen, A. M. Can. J. Chem. 1979, 57, 3168-3170, The values for 4-subsituted oxazoles, on the other hand, are 210 and 230 Hz for CH(14) and CH(19), respectively.
  • 7
    • 61349091800 scopus 로고    scopus 로고
    • So far we obtained only amorphic material
    • So far we obtained only amorphic material.
  • 8
    • 61349126293 scopus 로고    scopus 로고
    • -.
    • -.
  • 9
    • 61349141358 scopus 로고    scopus 로고
    • For complete absolute configuration of 1, taumycin A or a derivative including C-9 will have to be analyzed by X-ray.
    • For complete absolute configuration of 1, taumycin A or a derivative including C-9 will have to be analyzed by X-ray.
  • 10
    • 61349103845 scopus 로고    scopus 로고
    • 7Na 557.3197).
    • 7Na 557.3197).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.