Targeting of tumour cells with polyamine-drug conjugates.
作者信息
Cullis P M, Green R E, Malone M E, Merson-Davies L, Weaver R
机构信息
Centre for Mechanisms of Human Toxicity, University of Leicester.
出版信息
Biochem Soc Trans. 1994 Nov;22(4):402S. doi: 10.1042/bst022402s.
PMID:7698424
Abstract
摘要
相似文献
1
Targeting of tumour cells with polyamine-drug conjugates.用多胺-药物偶联物靶向肿瘤细胞。
Biochem Soc Trans. 1994 Nov;22(4):402S. doi: 10.1042/bst022402s.
2
Targeting of tumor cells and DNA by a chlorambucil-spermidine conjugate.苯丁酸氮芥-亚精胺缀合物对肿瘤细胞和DNA的靶向作用
Cancer Res. 1992 Aug 1;52(15):4190-5.
3
Selective labelling of cell-surface polyamine-binding proteins on leukaemic and solid-tumour cell types using a new polyamine photoprobe.使用一种新型多胺光探针选择性标记白血病和实体瘤细胞类型上的细胞表面多胺结合蛋白。
Biochem J. 1997 Dec 15;328 ( Pt 3)(Pt 3):889-95. doi: 10.1042/bj3280889.
4
Synthesis of spermidine and norspermidine dimers as high affinity polyamine transport inhibitors.
Bioorg Med Chem Lett. 1999 Jun 21;9(12):1709-14. doi: 10.1016/s0960-894x(99)00262-0.
5
Aliphatic chain length specificity of the polyamine transport system in ascites L1210 leukemia cells.腹水型L1210白血病细胞中多胺转运系统的脂肪族链长度特异性
Cancer Res. 1984 Jan;44(1):126-8.
6
Targeting the polyamine transport system with benzazepine- and azepine-polyamine conjugates.用苯并氮杂䓬-和氮杂䓬-多胺缀合物靶向多胺转运系统。
J Med Chem. 2010 Nov 11;53(21):7647-63. doi: 10.1021/jm1007648.
7
A comparison of chloroambucil- and xylene-containing polyamines leads to improved ligands for accessing the polyamine transport system.对含有苯丁酸氮芥和二甲苯的多胺进行比较，得到了用于进入多胺转运系统的改良配体。
J Med Chem. 2008 Mar 13;51(5):1393-401. doi: 10.1021/jm070794t. Epub 2008 Feb 19.
8
Polyamine transport in cells.细胞中的多胺转运
Biochem Soc Trans. 1994 Nov;22(4):894-8. doi: 10.1042/bst0220894.
9
Effects of chronic 5'-([(Z)-4-amino-2-butenyl]methylamino)-5'-deoxy- adenosine (AbeAdo) treatment on polyamine and eIF-5A metabolism in AbeAdo-sensitive and -resistant L1210 murine leukaemia cells.慢性5'-([(Z)-4-氨基-2-丁烯基]甲基氨基)-5'-脱氧腺苷（AbeAdo）处理对AbeAdo敏感和耐药的L1210小鼠白血病细胞中多胺和真核起始因子5A（eIF-5A）代谢的影响
Biochem J. 1993 Feb 15;290 ( Pt 1)(Pt 1):115-21. doi: 10.1042/bj2900115.
10
Cellular characterization of a new irreversible inhibitor of S-adenosylmethionine decarboxylase and its use in determining the relative abilities of individual polyamines to sustain growth and viability of L1210 cells.一种新型S-腺苷甲硫氨酸脱羧酶不可逆抑制剂的细胞特性及其在确定单个多胺维持L1210细胞生长和活力的相对能力中的应用。
Biochem J. 1989 Apr 15;259(2):325-31. doi: 10.1042/bj2590325.
Zotero 插件