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将四种新合成的2-氯乙基亚硝脲与卡莫司汀、洛莫司汀、司莫司汀、链脲佐菌素和羟乙基亚硝脲在晚期大鼠白血病L 5222中进行比较研究。

Examination of four newly synthesized 2-chloroethylnitrosoureas in comparison with BCNU, CCNU, MeCCNU, chlorozotocin and hydroxyethyl-CNU in preterminal rat leukemia L 5222.

作者信息

Zeller W J, Eisenbrand G, Fiebig H H

出版信息

J Cancer Res Clin Oncol. 1979 Sep;95(1):43-9. doi: 10.1007/BF00411108.

DOI:10.1007/BF00411108
PMID:159309
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12253729/
Abstract

The newly synthesized nitrosoureas 1-(2-chloroethyl)-1-nitroso-3-(methylenecarboxamido)-urea (Acetamido-CNU), 1-(2-chloroethyl)-1-nitroso-3-(4-morpholino)-urea (Morpholino-CNU), 1-(2-chloroethyl)-1-nitroso-3-(1-piperidino)-urea (Piperidino-CNU), and 2-[3-(2-chloroethyl)-3-nitrosoureido]-ethylmethanesulfonate (Ethylmethanesulfonato-CNU) were compared in their chemotherapeutic activity against preterminal rat leukemia L 5222 with BCNU, CCNU, MeCCNU, Chlorozotocin, and Hydroxyethyl-CNU. With respect to the dose range effecting a median survival time of more than 90 days, MeCCNU was superior to the other substances. Chlorozotocin, on the other hand, was the only substance which achieved no cures in this experimental arrangement. From the four newly introduced substances the water-soluble substances Acetamido-CNU and Morpholino-CNU were approximately comparable to CCNU with regard to the dose range effecting a median survival time of greater than 90 days. Piperidino-CNU and Ethylmethanesulfonato-CNU also effected cures; however, only Piperidino-CNU in one dosage effected a median survival time of greater than 90 days.

摘要

将新合成的亚硝基脲类化合物1-(2-氯乙基)-1-亚硝基-3-(亚甲基甲酰胺基)脲(乙酰氨基-CCNU)、1-(2-氯乙基)-1-亚硝基-3-(4-吗啉代)脲(吗啉代-CCNU)、1-(2-氯乙基)-1-亚硝基-3-(1-哌啶基)脲(哌啶基-CCNU)和2-[3-(2-氯乙基)-3-亚硝基脲基]乙烷磺酸盐(乙烷磺酸盐-CCNU)与卡莫司汀(BCNU)、洛莫司汀(CCNU)、司莫司汀(MeCCNU)、氯脲霉素和羟乙基亚硝基脲在对终末期前大鼠白血病L 5222的化疗活性方面进行了比较。就影响中位生存时间超过90天的剂量范围而言,MeCCNU优于其他物质。另一方面,氯脲霉素是在这种实验安排中唯一未实现治愈的物质。从四种新引入的物质来看,水溶性物质乙酰氨基-CCNU和吗啉代-CCNU在影响中位生存时间大于90天的剂量范围方面与CCNU大致相当。哌啶基-CCNU和乙烷磺酸盐-CCNU也实现了治愈;然而,只有一种剂量的哌啶基-CCNU实现了中位生存时间大于90天。

相似文献

1
Examination of four newly synthesized 2-chloroethylnitrosoureas in comparison with BCNU, CCNU, MeCCNU, chlorozotocin and hydroxyethyl-CNU in preterminal rat leukemia L 5222.将四种新合成的2-氯乙基亚硝脲与卡莫司汀、洛莫司汀、司莫司汀、链脲佐菌素和羟乙基亚硝脲在晚期大鼠白血病L 5222中进行比较研究。
J Cancer Res Clin Oncol. 1979 Sep;95(1):43-9. doi: 10.1007/BF00411108.
2
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The effectiveness and cost-effectiveness of carmustine implants and temozolomide for the treatment of newly diagnosed high-grade glioma: a systematic review and economic evaluation.卡莫司汀植入剂与替莫唑胺治疗新诊断的高级别胶质瘤的有效性和成本效益:一项系统评价与经济学评估
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Chemotherapeutic activity of new 2-chloroethylnitrosoureas in rat L5222 leukemia: comparison of bifunctional and water-soluble derivatives with 1,3-bis(2-chloroethyl)-1-nitrosourea.
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引用本文的文献

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本文引用的文献

1
[Leukemia L 5222 of the rat strain BD IX. An ethylnitrosourea-induced monocytic-myeloic transplantable form for cytochemical and chemotherapeutic studies].[大鼠BD IX品系的白血病L 5222。一种乙基亚硝基脲诱导的单核细胞-髓细胞可移植形式,用于细胞化学和化疗研究]
Blut. 1974 Apr;28(4):288-92. doi: 10.1007/BF01631649.
2
Chemotherapy of the transplantable acute leukemia L5222 in rats.大鼠可移植性急性白血病L5222的化学疗法。
Cancer Res. 1975 May;35(5):1168-74.
3
The nitrosoureas--thoughts for the future.亚硝基脲类——对未来的思考
Cancer Treat Rep. 1976 Jun;60(6):807-11.
4
Chemotherapeutic activity of new 2-chloroethylnitrosoureas in rat L5222 leukemia: comparison of bifunctional and water-soluble derivatives with 1,3-bis(2-chloroethyl)-1-nitrosourea.
J Natl Cancer Inst. 1978 Feb;60(2):345-8. doi: 10.1093/jnci/60.2.345.
5
Some new congeners of the anticancer agent 1,3-bis(2-chloroethyl)-1-nitrosourea (BCNU). Synthesis of bifunctional analogs and water soluble derivatives and preliminary evaluation of their chemotherapeutic potential.抗癌剂1,3-双(2-氯乙基)-1-亚硝基脲(卡莫司汀)的一些新同系物。双功能类似物和水溶性衍生物的合成及其化疗潜力的初步评估。
Z Krebsforsch Klin Onkol Cancer Res Clin Oncol. 1976 Aug 30;86(3):279-86. doi: 10.1007/BF00286946.
6
Synthesis of chlorozotocin, the 2-chloroethyl analog of the anticancer antibiotic streptozotocin.抗癌抗生素链脲佐菌素的2-氯乙基类似物氯脲佐菌素的合成。
J Med Chem. 1975 Jan;18(1):104-6. doi: 10.1021/jm00235a023.