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Potential CNS antitumor agents VI: aziridinylbenzoquinones III.

作者信息

Driscoll J S, Dudeck L, Congleton G, Geran R I

出版信息

J Pharm Sci. 1979 Feb;68(2):185-8. doi: 10.1002/jps.2600680217.

DOI:10.1002/jps.2600680217
PMID:423089
Abstract

Thirty-one aziridinylbenzoquinones were compared against five murine tumor models in vivo. Two intracerebral (ependymoblastoma and L-1210 leukemia) and three intraperitoneal (P-388 and L-1210 leukemia and B16 melanoma) systems were utilized. Excellent activity was observed for many compounds. Multiple long-term survivors were produced in the ependymoblastoma, P-388, and intraperitoneal L-1210 systems. Diethyl 2,5-bis(1-aziridinyl)-3,6-dioxo-1,4-cyclohexadiene-1,4-dicarbamate demonstrated superior activity in all five test systems. This compound also was reproducibly active against two colon tumors, a mammary tumor, and the intracerebrally implanted P-388 leukemia model.

摘要

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引用本文的文献

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The pharmacologic fate of 2,5-diaziridinyl-3,6-bis(carboethoxyamino) 1,4-benzoquinone (AZQ NSC-182986) by intracarotid or intravenous administration in beagles.
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Survival and cell cycle kinetics responses of Chinese hamster ovary cells, and clones of human adenocarcinoma of the stomach and astrocytoma to diaziquone (AZQ) in vitro.中国仓鼠卵巢细胞、人胃腺癌克隆及星形细胞瘤在体外对重氮醌(AZQ)的存活及细胞周期动力学反应。
Invest New Drugs. 1983;1(1):11-9. doi: 10.1007/BF00180187.
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J Neurooncol. 1983;1(1):15-9. doi: 10.1007/BF00153636.
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