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N-(Phosphonacetyl)-L-aspartate (PALA): current status.

作者信息

Rozencweig M, Abele R, Piccart M, Von Hoff D D, Muggia F M

出版信息

Recent Results Cancer Res. 1980;74:72-7. doi: 10.1007/978-3-642-81488-4_10.

DOI:10.1007/978-3-642-81488-4_10
PMID:7444151
Abstract

N-(Phosphonoacetyl)-L-aspartate (PALA) is a synthetic antimetabolite exhibiting striking oncolytic properties against a wide variety of experimental solid tumors. The clinical dose-limiting factor is mucocutaneous toxicity which is reversible and dose-related. Delineation of the single-agent activity of PALA in human cancer must still await results of recently activated trials.

摘要

相似文献

1
N-(Phosphonacetyl)-L-aspartate (PALA): current status.
Recent Results Cancer Res. 1980;74:72-7. doi: 10.1007/978-3-642-81488-4_10.
2
An overview of the clinical pharmacology of N-phosphonacetyl-L-aspartate (PALA), a new antimetabolite.
Recent Results Cancer Res. 1980;74:65-71. doi: 10.1007/978-3-642-81488-4_9.
3
Effects of N-(phosphonacetyl)-L-aspartate on murine tumors and normal tissues in vivo and in vitro and the relationship of sensitivity to rate of proliferation and level of aspartate transcarbamylase.N-(膦酰基乙酰基)-L-天冬氨酸对小鼠肿瘤及正常组织的体内外作用以及敏感性与增殖速率和天冬氨酸转氨甲酰酶水平的关系
Cancer Res. 1978 Feb;38(2):371-8.
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Aspartate carbamoyltransferase activity, drug concentrations, and pyrimidine nucleotides in tissue from patients treated with N-(phosphonacetyl)-L-aspartate.接受N-(膦酰乙酰基)-L-天冬氨酸治疗患者组织中的天冬氨酸氨甲酰转移酶活性、药物浓度及嘧啶核苷酸
Biochem Pharmacol. 1982 Oct 15;31(20):3317-21. doi: 10.1016/0006-2952(82)90567-6.
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Flux through the de novo pyrimidine pathway in vivo. Effect of N-phosphonacetyl-L-aspartate, a potent inhibitor of aspartate transcarbamylase.体内从头嘧啶途径的通量。天冬氨酸转氨甲酰酶的强效抑制剂N-膦酰乙酰-L-天冬氨酸的作用。
J Biol Chem. 1983 Nov 25;258(22):13564-9.
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N-(Phosphonacetyl)-L-aspartate inhibition of the enzyme complex of pyrimidine biosynthesis.N-(膦酰基乙酰基)-L-天冬氨酸对嘧啶生物合成酶复合物的抑制作用
Biochem Pharmacol. 1982 Oct 15;31(20):3313-6. doi: 10.1016/0006-2952(82)90566-4.
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Mechanism of resistance of variants of the Lewis lung carcinoma to N-(phosphonacetyl)-L-aspartic acid.Lewis肺癌变体对N-(膦酰乙酰基)-L-天冬氨酸的耐药机制
Cancer Res. 1981 Mar;41(3):894-904.
8
Pharmacological disposition of N-(phosphonacetyl)-L-aspartate in humans.N-(膦酰基乙酰基)-L-天冬氨酸在人体中的药物处置
Cancer Res. 1980 Jan;40(1):86-90.
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Enzymatic assay for the antitumor agent-N-(phosphonacetyl)-L-aspartic acid (PALA).抗肿瘤药物N-(膦酰乙酰基)-L-天冬氨酸(PALA)的酶活性测定
Cancer Treat Rep. 1979 Jan;63(1):85-8.
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Collateral sensitivity to N-(phosphonacetyl)-L-aspartic acid in a line of P388 leukemia cells selected for resistance to L-(alpha S, 5S)-alpha-amino-3- chloro-4,5-dihydro-5-isoxazoleacetic acid (acivicin).对N-(膦酰基乙酰基)-L-天冬氨酸的 collateral 敏感性在一株对L-(αS,5S)-α-氨基-3-氯-4,5-二氢-5-异恶唑乙酸(阿西维辛)产生抗性的P388白血病细胞系中。 (注:“collateral”这里可能是专业术语“旁系的”之类意思,具体准确意思需结合专业知识进一步确定)
Cancer Res. 1983 Apr;43(4):1598-601.

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