Fluorinated retinoic acids and their analogs. 2. Synthesis and biological activity of aromatic 4-fluoro analogs
作者:Ka-Kong Chan、Anthony C. Specian、Beverly A. Pawson
DOI:10.1021/jm00133a020
日期:1981.1
synthesis of this compound was achieved by condensation of 4-fluoro aldehyde 7 or 8 with the aromatic phosphonium salt 9a. Several analogues (101-e) having different substituted aromatic moieties were also prepared and tested for their antipapilloma effect. The monochloro analogue 10b was shown to have comparable activity to the parent compound 10a.
已发现(E,Z,E,E)-3,7-二甲基-4-氟-9-(4-甲氧基-2,3,6-三甲基苯基)壬酸酯戊酸酯(10a)在化学上引起明显的降解诱发小鼠皮肤乳头状瘤。该化合物的新合成通过使4-氟醛7或8与芳族phospho盐9a缩合而实现。还制备了具有不同取代的芳族部分的几种类似物(101-e),并测试了其抗乳头状瘤的作用。已证明一氯类似物10b具有与母体化合物10a相当的活性。