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长叶刺蒺藜根的细胞毒性和抗疟成分。

Cytotoxic and antimalarial constituents of the roots of Eurycoma longifolia.

作者信息

Kardono L B, Angerhofer C K, Tsauri S, Padmawinata K, Pezzuto J M, Kinghorn A D

机构信息

Department of Medicinal Chemistry and Pharmacognosy, College of Pharmacy, University of Illinois, Chicago 60612.

出版信息

J Nat Prod. 1991 Sep-Oct;54(5):1360-7. doi: 10.1021/np50077a020.

Abstract

By bioactivity-directed fractionation, five cytotoxic constituents have been characterized from the roots of Eurycoma longifolia collected in Kalimantan, Indonesia. Four canthin-6-one alkaloids, namely, 9-methoxycanthin-6-one, 9-methoxycanthin-6-one-N-oxide, 9-hydroxycanthin-6-one, and 9-hydroxycanthin-6-one-N-oxide, and one quassinoid, eurycomanone, were found to be cytotoxic principles. Each of these compounds was evaluated against a panel of cell lines comprising a number of human cancer cell types [breast, colon, fibrosarcoma, lung, melanoma, KB, and KB-V1 (a multi-drug resistant cell line derived from KB)] and murine lymphocytic leukemia (P-388). The canthin-6-ones 1-4 were found to be active with all cell lines tested except for the KB-V1 cell line. Eurycomanone was inactive against murine lymphocytic leukemia (P-388) but was significantly active against the human cell lines tested. Two additional isolates, the beta-carboline alkaloids beta-carboline-1-propionic acid and 7-methoxy-beta-carboline-1-propionic acid, were not significantly active with these cultured cells. However, compounds 5 and 7 were found to demonstrate significant antimalarial activity as judged by studies conducted with cultured Plasmodium falciparum strains. The structures of the novel compounds 2-4 and 7 were established by spectral and chemical methods.

摘要

通过生物活性导向的分级分离,从印度尼西亚加里曼丹采集的长叶刺蕊草根部鉴定出了五种具有细胞毒性的成分。发现四种咔啉-6-酮生物碱,即9-甲氧基咔啉-6-酮、9-甲氧基咔啉-6-酮-N-氧化物、9-羟基咔啉-6-酮和9-羟基咔啉-6-酮-N-氧化物,以及一种苦木素类化合物刺蒺藜皂甙,是细胞毒性成分。对这些化合物中的每一种都针对一组细胞系进行了评估,该细胞系包括多种人类癌细胞类型[乳腺癌、结肠癌、纤维肉瘤、肺癌、黑色素瘤、KB细胞系以及KB-V1细胞系(一种源自KB细胞系的多药耐药细胞系)]和小鼠淋巴细胞白血病(P-388)。发现咔啉-6-酮1-4对除KB-V1细胞系之外的所有测试细胞系均有活性。刺蒺藜皂甙对小鼠淋巴细胞白血病(P-388)无活性,但对所测试的人类细胞系有显著活性。另外两种分离物,β-咔啉生物碱β-咔啉-1-丙酸和7-甲氧基-β-咔啉-1-丙酸,对这些培养细胞无显著活性。然而,通过对培养的恶性疟原虫菌株进行研究判断,化合物5和7表现出显著的抗疟活性。通过光谱和化学方法确定了新化合物2-4和7的结构。

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