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S-(+)-脱氧娃儿藤定碱的抗癌作用和神经毒性,一种可与核酸相互作用的新型菲并吲哚里西啶生物碱

Anticancer effect and neurotoxicity of S-(+)-deoxytylophorinidine, a new phenanthroindolizidine alkaloid that interacts with nucleic acids.

作者信息

Liu Zhen-Jia, Lv Hai-Ning, Li Hong-Yan, Zhang Yi, Zhang Hai-Jing, Su Fu-Qin, Si Yi-Kang, Yu Shi-Shan, Chen Xiao-Guang

机构信息

Department of Pharmacology, Institute of Materia Medica, Peking Union Medical College & Chinese Academy of Medical Sciences, Beijing, China.

出版信息

J Asian Nat Prod Res. 2011 May;13(5):400-8. doi: 10.1080/10286020.2011.566868.

Abstract

Phenanthroindolizidine alkaloids are a family of plant-derived compounds with significant antineoplastic activity as well as other effects like antiamebicidal, antiviral, and anti-inflammatory activities. The specific biomolecular targets of these compounds have not yet been clearly identified. S-(+)-Deoxytylophorinidine (CAT) is a new phenanthroindolizidine alkaloid, originally extracted from the roots of Tylophora atrofolliculata and Tylophora ovata. Potent anticancer activity was observed in vitro and in vivo. Neurotoxicity of CAT was also studied and it was far less serious than that of vinblastine. Interactions between this compound and DNA had been studied in detail in our laboratory previously, and we further studied its interactions with RNA.

摘要

菲并吲哚里西啶生物碱是一类源自植物的化合物,具有显著的抗肿瘤活性以及其他作用,如抗阿米巴、抗病毒和抗炎活性。这些化合物的具体生物分子靶点尚未明确确定。S-(+)-脱氧娃儿藤定碱(CAT)是一种新的菲并吲哚里西啶生物碱,最初从卵叶娃儿藤和七层楼的根中提取。在体外和体内均观察到其强大的抗癌活性。还对CAT的神经毒性进行了研究,其神经毒性远比长春碱轻。此前我们实验室已详细研究了该化合物与DNA的相互作用,在此基础上我们进一步研究了其与RNA的相互作用。

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