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  • Actin-Aggregating Cucurbitacins from Physocarpus capitatus
    [作者:Maloney, KN; Fujita, M; Eggert, US; Schroeder, FC; Field, CM; Mitchison, TJ; Clardy, J,期刊:Journal of natural products, 页码:1927-1929 , 文章类型: Article,,卷期:2008年71-11]
  • Bioassay-guided fractionation of Physocarpus capitatus yielded two new cucurbitacins (3 and 4) along with the known cucurbitacin F (1) and dihydrocucurbitacin F (2). Preliminary mechanism of action studies indicate that ...
  • Total Synthesis of Bulbophylol-B
    [作者:Lin, JS; Zhang, W; Jiang, N; Niu, Z; Bao, K; Zhang, L; Liu, DL; Pan, C; Yao, XS,期刊:Journal of natural products, 页码:1938-1941 , 文章类型: Article,,卷期:2008年71-11]
  • The first total synthesis of bulbophylol-B (1) has been achieved with the longest linear sequence of 12 steps and an overall yield of 17.9% via a new and practical approach to construct the dihydrodibenz[b,f]oxepin skele...
  • Dihydrofurochromones from Prionosciadium thapsoides
    [作者:Torres-Valencia, JM; Chavez-Rios, OE; Cerda-Garcia-Rojas, CM; Burgueno-Tapia, E; Joseph-Nathan, P,期刊:Journal of natural products, 页码:1956-1960 , 文章类型: Article,,卷期:2008年71-11]
  • Chemical investigations of Prionosciadium thapsoides roots led to the isolation of the new dihydrofurochromones (S)-(+)-4 '-O-angeloyl-5-O-methylvisamminol (1) and (S)-(+)-4 '-O-senecioyl-5-O-methylvisamminol (2), togeth...
  • A Concise Synthesis of Pawhuskin A
    [作者:Neighbors, JD; Buller, MJ; Boss, KD; Wiemer, DF,期刊:Journal of natural products, 页码:1949-1952 , 文章类型: Article,,卷期:2008年71-11]
  • Pawhuskin A is an isoprenylated stilbene that was isolated from Dalea purpurea and reported to have affinity for the opioid receptor in vitro. It has been synthesized through a convergent sequence that joins a prenylated...
  • Direct Synthesis of Chrysosplenol D
    [作者:Kraus, G; Roy, S,期刊:Journal of natural products, 页码:1961-1962 , 文章类型: Article,,卷期:2008年71-11]
  • An aldol condensation and an Algar-Flynn-Oyamada oxidative cyclization were key steps in the direct synthesis of chrysosplenol D, an efflux pump inhibitor that can potentiate the activity of commercially important antibi...
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