Fluorinated retinoic acids and their analogs. 1. Synthesis and biological activity of (4-methoxy-2,3,6-trimethylphenyl)nonatetraenoic acid analogs
作者:Beverly A. Pawson、Ka-Kong Chan、James DeNoble、Ru Jen L. Han、Virginia Piermattie、Anthony C. Specian、Srisamorn Srisethnil、Patrick W. Trown、Oksana Bohoslawec
DOI:10.1021/jm00195a010
日期:1979.9
(4-Methoyx-2,3,6-trimethylphenyl)nonatetraenoic acids, esters, and amides (analogues of retinoic acid) bearing a fluorine atom(s) or a trifluoromethyl group on the polyene side chain were synthesized. The biological activities of these compounds and of 10-, 12-, and 14-fluororetinoic acid esters were evaluated in vivo in a chemically induced mouse papilloma test; the toxicities were assessed in an
合成了在多烯侧链上带有氟原子或三氟甲基的(4-甲基-2,3,6-三甲基苯基)壬酸酯链烯酸,酯和酰胺(视黄酸的类似物)。在化学诱导的小鼠乳头状瘤试验中评估了这些化合物以及10-,12-和14-氟维甲酸酸酯的生物活性。在体内小鼠维生素A超试验中评估了毒性。发现1c(12-氟维甲酸乙酯)和23和39(分别为芳族4和6-氟维甲酸酯)的抗乳头瘤瘤活性大于母体非氟化酯。相对于2,分别观察到71和72(芳族4-和6-氟视黄酸)和73(相对于4)的抗乳头瘤瘤活性增加。