Author:
Pischel Helmut,Holý Antonín,Veselý Jiří,Wagner Günther
Abstract
The title compounds were synthetized by the reaction of TRIS with p-nitrophenyl or alkyl esters of N-carboxymethyl derivatives of uracil, 5-chloro-, 5-bromo-, 5-iodouracil, thymine, cytosine, 6-azauracil, 2-pyridone, 2-pyrimidone, 3-pyridazone and orotic acid. The following novel N-carboxymethyl derivatives are also described: 6-azauracil derivative VIIa by condensation of 4-thio-6-azauracil with methyl bromoacetate followed by hydrolysis, 5-chloruracil derivative IIIa by chlorination of uracil compound IIa, 2-pyrimidone (IXa) and 3-pyridazone derivative Xa by the reaction of the sodium salts of the bases with sodium chloracetate. Of all the amides tested, only the 3-pyridazone derivative Xd and orotic acid derivative XIId inhibited the growth of L-1210 mouse leukemic cells in vitro with 1D50 approx. 10-4 mol l-1.
Publisher
Institute of Organic Chemistry & Biochemistry
Cited by
8 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Monitoring the chemical and physical stability for tromethamine excipient in a lipid based formulation by HPLC coupled with ELSD;Journal of Pharmaceutical and Biomedical Analysis;2015-11
2. References;Chemistry of Heterocyclic Compounds: A Series Of Monographs;2008-01-02
3. Prodrugs of Analogs of Nucleic Acid Components;Collection of Czechoslovak Chemical Communications;1994
4. Advances in Pyridazine Chemistry;Advances in Heterocyclic Chemistry Volume 49;1990
5. 1 Pharmacologically Active Pyridazine Derivatives. Part 1;Progress in Medicinal Chemistry;1990