氚标记抗疟药磷酸咯萘啶的研制

CAS OpenIR > 中科院上海原子核所2003年前

	氚标记抗疟药磷酸咯萘啶的研制
	江善根; 张留芳; 郑冬珠; 冯正; 吴祖帆
	1987-12-27
Source Publication	核技术
Issue	12
Abstract	<正> 根据一些抗疟药的构效关系;郑贤育等人合成了2-甲氧基-7-氯-10-[3′;5′-双(四氢吡咯次甲基)-4′-羟基苯胺基]苯骈[b]1;5-萘啶四磷酸盐;定名磷酸咯萘啶。磷酸咯萘啶为高效、低毒、与氯喹无交叉抗药性的疟原虫红内期裂殖体杀灭剂。为了进一步研究其在体内的吸收、分布和排泄过程;为临床合理用药提供依据;本文介绍了气液催化交换法制备氚标记磷酸咯萘啶。
Indexed By	CNKI
Language	中文
Funding Project	原子核所项目组
Document Type	期刊论文
Identifier	http://ir.sinap.ac.cn/handle/331007/11178
Collection	中科院上海原子核所2003年前
Recommended Citation GB/T 7714	江善根,张留芳,郑冬珠,等. 氚标记抗疟药磷酸咯萘啶的研制[J]. 核技术,1987(12).
APA	江善根,张留芳,郑冬珠,冯正,&吴祖帆.(1987).氚标记抗疟药磷酸咯萘啶的研制.核技术(12).
MLA	江善根,et al."氚标记抗疟药磷酸咯萘啶的研制".核技术 .12(1987).

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