Nakajima T, Masuda H, Okamoto T, Watanabe M, Yokoyama K, Yamada N, Tsukagoshi S, Taguchi T
Research Division, Green Cross Corporation, Osaka, Japan.
Gan To Kagaku Ryoho. 1990 Dec;17(12):2353-9.
HO-221, N-[4-(5-Bromo-2-pyrimidinyloxy)-3-chlorophenyl]-N'-(2-nitrobenzoyl ) urea is a novel benzoylphenylurea derivative. We had interested in various pharmacological actions of benzoylphenylurea compounds. Therefore, many compounds were synthetized and tested in various screening systems. In the process with these tests, we found HO-221 which showed an excellent antitumor activity. The antitumor activity of HO-221 was judged from the survival time and the tumor weight of experimented tumor-bearing animals. HO-221 preparation was orally administered. The compound exhibited significant effects against various animal tumors (P388, L1210, M5076, LLC, C38, S180, W256), and especially effective against the solid tumors. HO-221 was also markedly effective to MX-1 and LX-1 implanted into nude mice. However, the effect against mouse B16 melanoma was moderate. In addition, HO-221 showed a schedule dependency and once every 4 or 7 days treatments were most effective. The antitumor activities of the compound against advanced L1210 and Lewis lung tumors were examined. Tegafur and ara-C were used as reference drug for the study. Three agents showed the antitumor activities against L1210. Against Lewis lung carcinoma, HO-221 showed both the increase of life span and the tumor growth inhibition. On the other hand, tegafur and ara-C were ineffective for the increase of life span.
HO - 221,N - [4 - (5 - 溴 - 2 - 嘧啶氧基)-3 - 氯苯基]-N' - (2 - 硝基苯甲酰基)脲是一种新型苯甲酰基苯基脲衍生物。我们对苯甲酰基苯基脲化合物的多种药理作用感兴趣。因此,合成了许多化合物并在各种筛选系统中进行测试。在这些测试过程中,我们发现了具有优异抗肿瘤活性的HO - 221。HO - 221的抗肿瘤活性是根据实验性荷瘤动物的存活时间和肿瘤重量来判断的。HO - 221制剂通过口服给药。该化合物对多种动物肿瘤(P388、L1210、M5076、LLC、C38、S180、W256)均表现出显著效果,尤其对实体瘤有效。HO - 221对植入裸鼠体内的MX - 1和LX - 1也有明显效果。然而,对小鼠B16黑色素瘤的效果中等。此外,HO - 221显示出给药方案依赖性,每4天或7天给药一次最为有效。研究了该化合物对晚期L1210和Lewis肺癌的抗肿瘤活性。替加氟和阿糖胞苷用作该研究的参照药物。三种药物对L1210均显示出抗肿瘤活性。对于Lewis肺癌,HO - 221既延长了生存期又抑制了肿瘤生长。另一方面,替加氟和阿糖胞苷对延长生存期无效。