Wick M M, FitzGerald G B
Dana-Farber Cancer Institute, Department of Dermatology, Harvard Medical School, Boston, MA.
J Pharm Sci. 1987 Jul;76(7):513-5. doi: 10.1002/jps.2600760704.
This report describes a structure-activity analysis of isomers of three classes of dihydroxybenzene derivatives, including dihydroxybenzaldoxime, dihydroxybenzaldehyde, and dihydroxybenzonitrile. These derivatives were examined for their effect on ribonucleotide reductase activity, macromolecular synthesis, cell growth, and in vivo antitumor activity against the L1210 murine leukemia. One of the compounds studied exhibited significant antitumor activity against the growth of L1210 leukemia cells. A comparison of the various analogues revealed a possible correlation for 3,4-dihydroxybenzaldoxime between its potent inhibitory effect toward ribonucleotide reductase activity (IC50 = 38 microM) and its superior L1210 antitumor activity [percent increased life span (% ILS) = 100].
本报告描述了三类二羟基苯衍生物异构体的构效关系分析,这些衍生物包括二羟基苯甲醛肟、二羟基苯甲醛和二羟基苯甲腈。检测了这些衍生物对核糖核苷酸还原酶活性、大分子合成、细胞生长以及对L1210小鼠白血病的体内抗肿瘤活性的影响。所研究的化合物之一对L1210白血病细胞的生长表现出显著的抗肿瘤活性。对各种类似物的比较揭示了3,4 - 二羟基苯甲醛肟对核糖核苷酸还原酶活性的强效抑制作用(IC50 = 38 microM)与其优异的L1210抗肿瘤活性[寿命延长百分比(% ILS)= 100]之间可能存在的相关性。