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Alkylphosphocholines: a new class of membrane-active anticancer agents.

作者信息

Hilgard P, Klenner T, Stekar J, Unger C

机构信息

ASTA Medica AG, Frankfurt am Main.

出版信息

Cancer Chemother Pharmacol. 1993;32(2):90-5. doi: 10.1007/BF00685608.

DOI:10.1007/BF00685608
PMID:8485813
Abstract
摘要

相似文献

1
Alkylphosphocholines: a new class of membrane-active anticancer agents.烷基磷胆碱:一类新型的膜活性抗癌药物。
Cancer Chemother Pharmacol. 1993;32(2):90-5. doi: 10.1007/BF00685608.
2
The development of alkylphosphocholines as signal transduction inhibitors: experimental and clinical challenges.烷基磷胆碱作为信号转导抑制剂的研发:实验与临床挑战
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3
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Prog Exp Tumor Res. 1992;34:90-7. doi: 10.1159/000420835.
4
In vitro and in vivo antitumoral activity of alkylphosphonates.
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5
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Cancer Treat Rev. 1990 Sep;17(2-3):233-42. doi: 10.1016/0305-7372(90)90053-i.
6
Antineoplastic activity in vitro of free and liposomal alkylphosphocholines.游离型和脂质体型烷基磷胆碱的体外抗肿瘤活性
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Treatment of Schistosoma mansoni with miltefosine in vitro enhances serological recognition of defined worm surface antigens.用米替福新体外治疗曼氏血吸虫可增强对特定虫体表面抗原的血清学识别。
PLoS Negl Trop Dis. 2017 Aug 25;11(8):e0005853. doi: 10.1371/journal.pntd.0005853. eCollection 2017 Aug.
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Evaluation of the effect of miltefosine on Trichomonas vaginalis.评价米替福新对阴道毛滴虫的作用。
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Erufosine suppresses breast cancer in vitro and in vivo for its activity on PI3K, c-Raf and Akt proteins.依鲁替尼抑制乳腺癌的体外和体内活性与其对 PI3K、c-Raf 和 Akt 蛋白的作用有关。
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Perifosine , an oral, anti-cancer agent and inhibitor of the Akt pathway: mechanistic actions, pharmacodynamics, pharmacokinetics, and clinical activity.培非司亭,一种口服抗癌药和 Akt 通路抑制剂:作用机制、药效学、药代动力学和临床活性。
Expert Opin Drug Metab Toxicol. 2012 May;8(5):623-33. doi: 10.1517/17425255.2012.681376.
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Lysolipid containing liposomes for transendothelial drug delivery.用于跨内皮药物递送的含溶血脂质脂质体。
BMC Res Notes. 2012 Apr 10;5:179. doi: 10.1186/1756-0500-5-179.
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Potential involvement of F0F1-ATP(synth)ase and reactive oxygen species in apoptosis induction by the antineoplastic agent erucylphosphohomocholine in glioblastoma cell lines : a mechanism for induction of apoptosis via the 18 kDa mitochondrial translocator protein.反式-二十二碳烯基磷酰胆碱通过诱导 18kDa 线粒体转位蛋白诱导神经胶质瘤细胞凋亡:F0F1-ATP 合酶和活性氧的潜在作用
Apoptosis. 2010 Jul;15(7):753-68. doi: 10.1007/s10495-010-0460-5.
Enhancement of the antiproliferative effect of cis-diamminedichloroplatinum(II) and nitrogen mustard by inhibitors of protein kinase C.
蛋白激酶C抑制剂增强顺二氯二氨铂(II)和氮芥的抗增殖作用。
Int J Cancer. 1988 Sep 15;42(3):382-8. doi: 10.1002/ijc.2910420313.
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Characterization of the antitumor activity of hexadecylphosphocholine (D 18506).
Eur J Cancer Clin Oncol. 1988 Sep;24(9):1457-61. doi: 10.1016/0277-5379(88)90336-7.
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Specific interaction between phosphatidylinositol 4,5-bisphosphate and profilactin.磷脂酰肌醇4,5-二磷酸与肌动蛋白单体结合蛋白之间的特异性相互作用。
Nature. 1985;314(6010):472-4. doi: 10.1038/314472a0.
7
Synergistic enhancement of the antiproliferative activity of cis-diamminedichloroplatinum(II) by the ether lipid analogue BM41440, an inhibitor of protein kinase C.醚脂类似物BM41440(一种蛋白激酶C抑制剂)对顺二氨二氯铂(II)抗增殖活性的协同增强作用。
Lipids. 1989 Apr;24(4):312-7. doi: 10.1007/BF02535169.
8
The specific inhibitor of protein kinase C, 1-(5-isoquinolinylsulfonyl)-2-methylpiperazine (H7), induces morphological change and cell differentiation of human neural crest-derived cell lineages.蛋白激酶C的特异性抑制剂1-(5-异喹啉磺酰基)-2-甲基哌嗪(H7)可诱导人神经嵴衍生细胞系发生形态变化和细胞分化。
FEBS Lett. 1990 Aug 20;269(1):4-6. doi: 10.1016/0014-5793(90)81104-v.
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In vitro investigations on the antineoplastic effect of hexadecylphosphocholine.十六烷基磷胆碱抗肿瘤作用的体外研究。
Arzneimittelforschung. 1991 Jun;41(6):652-5.
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Hexadecylphosphocholine-mediated enhancement of T-cell responses to interleukin 2.
Cell Immunol. 1991 Oct 1;137(1):232-8. doi: 10.1016/0008-8749(91)90072-j.