Schneider M R, Schuderer M L
Sonderforschungsbereich 234, Institut für Pharmazie, Universität Regensburg, F.R.G.
Arch Pharm (Weinheim). 1990 Apr;323(4):215-9. doi: 10.1002/ardp.19903230407.
1-[4-N,N-bis-2-chloroethylcarbamoyloxy)-phenyl]-1-(4-hydroxyphenyl )-2- phenylbut-1-ene (1) is a cytotoxic estrogen with a selective antitumor effect only on estrogen receptor (ER) containing tumors. In order to improve the ER affinity and thereby the antitumor activity of 1 a second OH-group in position 3 or 4 was introduced into the phenyl ring at C-atom 2 (8 and 9) and the respective acetates 10 and 11 were prepared. These modifications caused an enhanced ER affinity of 8-11 as compared to 1. The estrogenic properties were only slightly increased. In vitro, an enhanced antitumor effect on the ER positive MCF-7 mammary tumor cell line was determined for 8-11 as compared to 1 leading to inhibitions up to 90%. In vivo, 8-11 caused a pronounced growth inhibition of the hormone-dependent MXT M3.2 mammary tumor of the mouse though these effects were not better than those caused by 1 except the acetate 10, which inhibited tumor growth by 88%. These data show that the introduction of a second OH-group into 1 not only increased ER affinity, but also the antitumor activity in vitro and to a lesser extent in vivo in ER positive tumors. As none of these compounds had any significant effect on ER negative tumor models, 8-11 can be regarded as cytotoxic estrogens with a specific ER-mediated effect selectively on ER positive tumors.
1-[4-N,N-双(2-氯乙基)氨甲酰氧基)苯基]-1-(4-羟基苯基)-2-苯基丁-1-烯(1)是一种细胞毒性雌激素,仅对含雌激素受体(ER)的肿瘤具有选择性抗肿瘤作用。为了提高ER亲和力,从而提高1的抗肿瘤活性,在C-原子2(8和9)的苯环上的3位或4位引入了第二个羟基,并制备了相应的乙酸酯10和11。与1相比,这些修饰导致8-11的ER亲和力增强。雌激素特性仅略有增加。在体外,与1相比,8-11对ER阳性MCF-7乳腺肿瘤细胞系的抗肿瘤作用增强,导致抑制率高达90%。在体内,8-11对小鼠激素依赖性MXT M3.2乳腺肿瘤有明显的生长抑制作用,尽管除乙酸酯10外,这些作用并不比1引起的作用更好,乙酸酯10抑制肿瘤生长88%。这些数据表明,在1中引入第二个羟基不仅增加了ER亲和力,而且在体外以及在较小程度上在体内对ER阳性肿瘤增加了抗肿瘤活性。由于这些化合物对ER阴性肿瘤模型均无显著影响,8-11可被视为具有特定ER介导作用的细胞毒性雌激素,对ER阳性肿瘤具有选择性作用。