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镧(III)与某些1-氨基环烷羧酸配合物的合成及其肿瘤抑制活性

Synthesis and tumor inhibiting activity of lanthanum (III) complexes with some 1-aminocycloalkancarboxylic acids.

作者信息

Kovachev T B, Ivanov D S, Buyukliev R T, Konstantinov S M, Karaivanova M C

机构信息

Department of Chemistry, Higher Medical School, Sofia, Bulgaria.

出版信息

Pharmazie. 1996 Jan;51(1):25-7.

PMID:8999429
Abstract

Complexes of La(III) with 1-aminocyclopentane-, -hexane, -heptane and -4-ethylcyclohexanecarboxylic acids were obtained. The compounds were characterized by elemental analyses, IR spectroscopy and conductivity measurements. The following general formula was derived: LaL3Cl3 x 5 H2O, where L is the corresponding 1-aminocycloalkanecarboxylic acid. The pharmacological studies showed that all complexes manifested higher cytostatic and cytotoxic effects in comparison with lanthanum chloride. Much higher cytotoxic (anti-P388/D1) and cytostatic (anti-L-1210 and anti-melanoma-B16) activity was found for the lanthanum complex with 1-aminocyclopentanecarboxylic acid.

摘要

制备了镧(III)与1-氨基环戊烷羧酸、1-氨基环己烷羧酸、1-氨基庚烷羧酸和4-乙基环己烷羧酸形成的配合物。通过元素分析、红外光谱和电导率测量对这些化合物进行了表征。推导得到如下通式:LaL₃Cl₃·5H₂O,其中L为相应的1-氨基环烷羧酸。药理学研究表明,与氯化镧相比,所有配合物均表现出更高的细胞抑制和细胞毒性作用。发现镧与1-氨基环戊烷羧酸形成的配合物具有更高的细胞毒性(抗P388/D1)和细胞抑制活性(抗L-1210和抗黑色素瘤-B16)。

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