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新型抗癌药物番茄甜菜碱(AT-1840)的构效关系研究

[Structure-activity-relationship study of the new anticancer drug lycobetaine (AT-1840)].

作者信息

He H M, Weng Z Y

出版信息

Yao Xue Xue Bao. 1989;24(4):302-4.

PMID:2816392
Abstract

Lycobetaine (AT-1840), developed by our institute, is a new chemotherapeutic agent with relatively high percentage of remission on the treatment of ovary cancer and stomach cancer; no remarkable changes in blood picture, EKG and GPT, were observed. Early examination of the structure activity relationship of lycobetaine gave the following results: 1. A potential betaine and a methylenedioxy group in this compound may be critical for exhibiting antitumor activity; 2. Fission of the five membered ring of lycobetaine will not affect its antitumor activity. In order to see whether the distance between the phenolic oxygen and quaternary nitrogen affects its antitumor activity, compounds 7a-c, 8a-b were synthesized and screened against tumor in mice bearing EAC Preliminary experimental results showed that among the open ring analogs of lycobetaine, 7a, 7b and 8d possessed marked antitumor activity and 7c did not. The results indicate that changes in the distance of the betaine in lycobetaine obviously influence its antitumor activity.

摘要

我院研制的石蒜碱(AT-1840)是一种新型化疗药物,对卵巢癌和胃癌的治疗有较高的缓解率;用药后血常规、心电图及谷丙转氨酶未见明显变化。早期对石蒜碱构效关系的研究结果如下:1. 该化合物中的潜在甜菜碱和亚甲二氧基可能对其抗肿瘤活性起关键作用;2. 石蒜碱五元环的开环不影响其抗肿瘤活性。为了考察酚羟基氧原子与季铵氮原子之间的距离是否影响其抗肿瘤活性,合成了化合物7a-c、8a-b,并对荷艾氏腹水癌(EAC)小鼠进行了抗肿瘤筛选。初步实验结果表明,在石蒜碱的开环类似物中,7a、7b和8d具有明显的抗肿瘤活性,而7c则无活性。结果表明,石蒜碱中甜菜碱距离的改变明显影响其抗肿瘤活性。

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