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1-(2-氯乙基)-3-异丁基-3-(β-麦芽糖基)-1-亚硝基脲对实验性肿瘤的作用

Effect of 1-(2-chloroethyl)-3-isobutyl-3-(beta-maltosyl)-1-nitrosourea on experimental tumors.

作者信息

Akaike Y, Arai Y, Taguchi H, Satoh H

出版信息

Gan. 1982 Jun;73(3):480-7.

PMID:7129012
Abstract

The antitumor activity of 1-(2-chloroethyl)-3-isobutyl-3-(beta-maltosyl)-1-nitrosourea (TA-077), a novel water-soluble nitrosourea derivative, against leukemia L1210, Ehrlich carcinoma, sarcoma 180, Lewis lung carcinoma, Yoshida sarcoma, rat ascites hepatomas and Walker 256 carcinosarcoma was examined and compared with those of 3 reference nitrosourea antitumor agents, 1-(2-chloroethyl)-3-(beta-D-glucopyranosyl)-1-nitrosourea, 3-[(4-amino-2-methyl-5-pyrimidinyl)methyl]-1-(2-chloroethyl)-1-nitrosourea hydrochloride and 1-(2-chloroethyl)-3-cyclohexyl-1-nitrosourea. TA-077 exhibited a broad antitumor spectrum against the above tumors. Among these 4 nitrosoureas, TA-077 produced the best therapeutic ratios (OD/ILS30) against leukemia L1210, irrespective of the administration route and schedule employed. The ratio obtained by consecutive treatment (ip) was superior to that by single administration, a unique characteristic of this novel nitrosourea agent. The inhibitory effect of TA-077 on the growth of non-syngenic tumors (solid form) was also significant in all administration routes employed (ip, iv and po). Furthermore, TA-077 showed a marked life-prolonging effect on both early and advanced forms of Lewis lung carcinoma.

摘要

新型水溶性亚硝基脲衍生物1-(2-氯乙基)-3-异丁基-3-(β-麦芽糖基)-1-亚硝基脲(TA-077)对白血病L1210、艾氏癌、肉瘤180、刘易斯肺癌、吉田肉瘤、大鼠腹水肝癌和沃克256癌肉瘤的抗肿瘤活性进行了研究,并与3种参考亚硝基脲抗肿瘤药物1-(2-氯乙基)-3-(β-D-吡喃葡萄糖基)-1-亚硝基脲、3-[(4-氨基-2-甲基-5-嘧啶基)甲基]-1-(2-氯乙基)-1-亚硝基脲盐酸盐和1-(2-氯乙基)-3-环己基-1-亚硝基脲进行了比较。TA-077对上述肿瘤表现出广泛的抗肿瘤谱。在这4种亚硝基脲中,无论采用何种给药途径和方案,TA-077对白血病L1210产生的治疗比率(OD/ILS30)最佳。连续给药(ip)获得的比率优于单次给药,这是这种新型亚硝基脲药物的独特特征。TA-077对非同基因肿瘤(实体形式)生长的抑制作用在所有采用的给药途径(ip、iv和po)中也很显著。此外,TA-077对刘易斯肺癌的早期和晚期形式均显示出显著的延长生命作用。

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