α-二氟甲基鸟氨酸（一种鸟氨酸脱羧酶的酶激活不可逆抑制剂）对小鼠L1210白血病的影响。 - Suppr

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超能文献

Effect of alpha-difluoromethylornithine, an enzyme-activated irreversible inhibitor of ornithine decarboxylase, on L1210 leukemia in mice.

作者信息

Prakash N J, Schechter P J, Grove J, Koch-Weser J

出版信息

Cancer Res. 1978 Sep;38(9):3059-62.

PMID:679213

Abstract

摘要

相似文献

Effect of alpha-difluoromethylornithine, an enzyme-activated irreversible inhibitor of ornithine decarboxylase, on L1210 leukemia in mice.α-二氟甲基鸟氨酸（一种鸟氨酸脱羧酶的酶激活不可逆抑制剂）对小鼠L1210白血病的影响。

Cancer Res. 1978 Sep;38(9):3059-62.

Comparison of the biological effects of four irreversible inhibitors of ornithine decarboxylase in two murine lymphocytic leukemia cell lines.两种小鼠淋巴细胞白血病细胞系中四种鸟氨酸脱羧酶不可逆抑制剂的生物学效应比较

Cancer Res. 1986 Mar;46(3):1148-54.

Effects of methylglyoxal-bis(guanylhydrazone) on polyamine metabolism in spleens of mice with disseminated L1210 lymphoid leukemia.甲基乙二醛双（脒腙）对患有播散性L1210淋巴细胞白血病小鼠脾脏中多胺代谢的影响。

Cancer Res. 1974 Apr;34(4):886-92.

Inhibition of early embryogenic development in mice by alpha-difluoromethyl ornithine, an enzyme-activated irreversible inhibitor of L-ornithine decarboxylase [proceedings].α-二氟甲基鸟氨酸（一种L-鸟氨酸脱羧酶的酶激活不可逆抑制剂）对小鼠早期胚胎发育的抑制作用[会议论文集]

Br J Pharmacol. 1979 Jul;66(3):436P-437P.

Ornithine decarboxylase and polyamines in tissues of the neonatal rat: effects of alpha-difluoromethylornithine, a specific, irreversible inhibitor of ornithine decarboxylase.新生大鼠组织中的鸟氨酸脱羧酶和多胺：鸟氨酸脱羧酶特异性不可逆抑制剂α-二氟甲基鸟氨酸的作用

J Pharmacol Exp Ther. 1982 Sep;222(3):741-5.

Independence of drug action on mitochondria and polyamines in L1210 leukemia cells treated with methylglyoxal-bis(guanylhydrazone).用甲基乙二醛双（脒腙）处理的L1210白血病细胞中药物作用对线粒体和多胺的独立性

Cancer Res. 1980 Dec;40(12):4533-40.

Further studies on difluoromethylornithine in African trypanosomes.关于二氟甲基鸟氨酸在非洲锥虫中的进一步研究。

Med Biol. 1981 Dec;59(5-6):434-40.

Antitumor properties of (2R,5R)-6-heptyne-2,5-diamine, a new potent enzyme-activated irreversible inhibitor of ornithine decarboxylase, in rodents.新型强效鸟氨酸脱羧酶酶激活不可逆抑制剂（2R,5R）-6-庚炔-2,5-二胺在啮齿动物中的抗肿瘤特性

Cancer Res. 1984 Nov;44(11):4972-7.

Independent regulation of ornithine decarboxylase and S-adenosylmethionine decarboxylase in methylthioadenosine phosphorylase-deficient malignant murine lymphoblasts.甲硫腺苷磷酸化酶缺陷型恶性小鼠淋巴母细胞中鸟氨酸脱羧酶和S-腺苷甲硫氨酸脱羧酶的独立调节

Cancer Res. 1985 Aug;45(8):3567-72.

Methylglyoxal BIS (guanylhydrazone) and alpha-difluoromethylornithine-induced polyamine deprivation in psoriatic lesions.甲基乙二醛双（胍基腙）和α-二氟甲基鸟氨酸诱导银屑病皮损中的多胺缺乏。

Acta Derm Venereol. 1982;62(3):221-4.

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Targeting the polyamine pathway-"a means" to overcome chemoresistance in triple-negative breast cancer.靶向多胺途径——克服三阴性乳腺癌化疗耐药性的“一种手段”。

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Beneficial effects of a polyamine biosynthesis inhibitor on lupus in MRL-lpr/lpr mice.多胺生物合成抑制剂对MRL-lpr/lpr小鼠狼疮的有益作用。

Clin Exp Immunol. 1989 Nov;78(2):239-44.

alpha-Difluoromethylornithine, an irreversible inhibitor of ornithine decarboxylase, inhibits tumor promoter-induced polyamine accumulation and carcinogenesis in mouse skin.α-二氟甲基鸟氨酸是鸟氨酸脱羧酶的不可逆抑制剂，可抑制肿瘤启动子诱导的小鼠皮肤多胺积累和致癌作用。

Proc Natl Acad Sci U S A. 1982 Oct;79(19):6028-32. doi: 10.1073/pnas.79.19.6028.

Effects of DL-alpha-difluoromethylornithine, an irreversible inhibitor of ornithine decarboxylase, on the rat mammary tumour induced by 7,12-dimethylbenz[a]anthracene.鸟氨酸脱羧酶不可逆抑制剂DL-α-二氟甲基鸟氨酸对7,12-二甲基苯并[a]蒽诱导的大鼠乳腺肿瘤的影响。

Naunyn Schmiedebergs Arch Pharmacol. 1982 Jul;320(1):72-7. doi: 10.1007/BF00499076.

Response of enzymes involved in the metabolism of polyamines to phytohaemagglutinin-induced activation of human lymphocytes.多胺代谢相关酶对植物血凝素诱导的人淋巴细胞激活的反应。

Biochem J. 1981 Jun 15;196(3):733-8. doi: 10.1042/bj1960733.

Regulation of S-adenosylmethionine decarboxylase by polyamines in Ehrlich ascites-carcinoma cells grown in culture.多胺对培养的艾氏腹水癌细胞中S-腺苷甲硫氨酸脱羧酶的调节作用

Biochem J. 1980 Sep 15;190(3):747-54. doi: 10.1042/bj1900747.

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