CAS: 16790-93-5; Methyl (6S,6As,7S,9R,11S)-7-((S)-1-Hydroxyethyl)-2,3-Dimethoxy-7,8,9,10,12,13-Hexahydro-5H-6,9-Methanopyrido[1',2':1,2]Azepino[4,5-B]Indole-6(6Ah)-Carboxylate

该化合物是一种生物活性藻类,产自同系菌种,其显著之处在于其19(S)位置的立体特定水分突变,这一结构特征增强了其与某些生物目标的紧密性,使其对药理研究很有价值.复合物作为合成更复杂的藻类或作为分析研究参考标准的前体的潜力.其定义明确的立体化学确保实验应用的可复制性. 19(S)-Hydroxycoopyngine由于与...

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榴花碱 Conopharyngine 76-98-2

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    📜榴花碱 反应生成20-羟基榴花碱
    参考文献:Terpenoid Indole Alkaloid Biotransformation Capacity Of Suspension Cultures Of Tabernaemontana Divaricata
    标题:Terpenoid Indole Alkaloid Biotransformation Capacity Of Suspension Cultures Of Tabernaemontana Divaricata
    摘要:Two Cell Lines Of Tabernaemontana Divaricata Derived From The Same Suspension Culture Were Compared With Respect To Their Biotransformation Capacity. One Is A High Indole Alkaloid-Producing Culture Which Accumulated Mainly O-Acetylvallesamine. The Other Cell Line Biosynthesizes Terpehoid Indole Alkaloids In Much Lower Amounts. Both Cell Lines Were Cultured In Medium Containing Either Conopharyngine,Coronaridine,Vobasine Or Tabersonine. Chemical Breakdown Was Followed In Fresh And Used Culture Medium In The Absence Of Cell Culture. All The Alkaloids Investigated Underwent Chemical Transformation. Most Of The Biotransformation Products Accumulated By The Cultures Have Been Reported To occur In Intact Plants. Since All The Alkaloids Added Were Transformed In The Same Way By Both Cultures,The Two Cell Lines Seem To Have The Same Biotransformation Potential.
    Doi:10.1016/s0031-9422(00)90584-3

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    参考文献:10.5281/zenodo.5794106
    摘要:The LOTUS Initiative for Open Natural Products Research: frozen dataset union wikidata (with metadata) | DOI:10.5281/zenodo.5794106
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