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Estudo químico de Sinningia allagophylla guiado por testes de atividade antiproliferativa

机译:抗增生活性试验指导的苦参化学研究

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Activity guided fractionation of Sinningia allagophylla (Mart.) Wiehler ethanolic extract yielded a new benzochromene 8-methoxylapachenol, besides seven known compounds: lapachenol, sitosteryl oleate, sitosteryl linoleate, stigmasteryl oleate, stigmasteryl linoleate, dunniol and tectoquinone. Extract, fractions, and compounds lapachenol, 8-methoxylapachenol, and dunniol were tested in vitro against human cancer cell lines U251 (glioma, CNS), MCF-7 (breast), NCI-ADR/RES (drug-resistant ovarian), 786-0 (kidney), NCI-H460 (lung, no small cells), PC-3 (prostate), OVCAR-3 (ovarian), HT-29 (colon), K562 (leukemia) and against VERO, a normal cell line. The most active compound was dunniol, which inhibited the growth of U251, MCF-7, NCI-ADR/RES, OVCAR-3 and K562 cell lines.
机译:活性指导的Sinningia allagophylla(Mart。)Wiehler乙醇提取物的分馏,除了七种已知化合物外,还产生了新的苯并色烯8-甲氧基拉帕基诺尔:拉帕基诺尔,谷甾醇油酸酯,谷甾醇亚油酸酯,豆甾醇甾烯酸酯,豆甾醇甾烯酸酯,丁烯醇和tectoquinone。提取物,级分和化合物lapachenol,8-methoxylapachenol和dunniol在体外针对人癌细胞系U251(神经胶质瘤,CNS),MCF-7(乳腺癌),NCI-ADR / RES(抗药性卵巢癌)786 -0(肾脏),NCI-H460(肺,无小细胞),PC-3(前列腺),OVCAR-3(卵巢),HT-29(结肠),K562(白血病)和针对正常细胞系的VERO 。最具活性的化合物是丁诺醇,它可以抑制U251,MCF-7,NCI-ADR / RES,OVCAR-3和K562细胞系的生长。

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