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首页> 外文期刊>Angewandte Chemie >Enantioselective Synthesis of(+)-Chamaecypanone C:A Novel Microtubule Inhibitor
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Enantioselective Synthesis of(+)-Chamaecypanone C:A Novel Microtubule Inhibitor

机译:对映体合成的(+)-Chamaecypanone C:新型微管抑制剂

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摘要

A number of bicyclo[2.2.2]octenone-containing natural products have been isolated from the heartwood of Chamaecy-paris obtusa var.formosana(Scheme 1), including the Diels-Alder(DA)adducts obtunone(1)and chamaecypa-none C(2), as well as the [4+2] dimer(+)-3.(+)-2 has been shown to exhibit potent cytotoxicity against several human cancer cells, including human oral epidermoid carcinoma(KB;IC_(50)= 190nM).
机译:从Chamaecy-paris obtusa var.formosana(方案1)的心材中分离了许多含双环[2.2.2]辛烯酮的天然产物,包括Diels-Alder(DA)加合物obtunone(1)和chamaecypa-none C(2)以及[4 + 2]二聚体(+)-3。(+)-2已显示出对几种人类癌细胞的有效细胞毒性,包括人类口腔表皮样癌(KB; IC_(50 )= 190nM)。

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