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DNA binding studies on several new anthracycline antitumor antibiotics II. The importance of the carbomethoxy-group as position-10 of the class II anthracycline molecule.

作者信息

DuVernay V H, Pachter J A, Crooke S T

出版信息

Mol Pharmacol. 1979 Sep;16(2):623-32.

PMID:514262
Abstract
摘要

相似文献

1
DNA binding studies on several new anthracycline antitumor antibiotics II. The importance of the carbomethoxy-group as position-10 of the class II anthracycline molecule.
Mol Pharmacol. 1979 Sep;16(2):623-32.
2
The antitumor effects of anthracyclines. II. The stereospecificity of the carbomethoxy group at position 10 of the class II anthracycline molecule.蒽环类药物的抗肿瘤作用。II. II类蒽环类分子10位碳甲氧基的立体特异性。
Mol Pharmacol. 1982 Jan;21(1):196-203.
3
Association of anthracycline derivatives with DNA: a fluorescence study.蒽环类衍生物与DNA的结合:一项荧光研究。
Farmaco Sci. 1985 Jun;40(6):377-90.
4
Parsing the free energy of anthracycline antibiotic binding to DNA.解析蒽环类抗生素与DNA结合的自由能。
Biochemistry. 1996 Feb 20;35(7):2047-53. doi: 10.1021/bi952812r.
5
Fluorescence polarization studies of the binding of BMS 181176 to DNA.BMS 181176与DNA结合的荧光偏振研究。
J Biomol Struct Dyn. 1994 Dec;12(3):625-36. doi: 10.1080/07391102.1994.10508763.
6
Change of the sequence specificity of daunorubicin-stimulated topoisomerase II DNA cleavage by epimerization of the amino group of the sugar moiety.通过糖部分氨基的差向异构化改变柔红霉素刺激的拓扑异构酶II DNA切割的序列特异性。
Cancer Res. 1995 Jan 15;55(2):312-7.
7
DNA topoisomerase II-mediated interaction of doxorubicin and daunorubicin congeners with DNA.DNA拓扑异构酶II介导的阿霉素和柔红霉素类似物与DNA的相互作用。
Cancer Res. 1989 Nov 1;49(21):5969-78.
8
Joint experimental and theoretical investigation of the comparative DNA binding affinities of intercalating anthracycline derivatives.
Mol Pharmacol. 1989 Feb;35(2):251-6.
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Anti-cancer activity of anthracycline antibiotics and DNA condensation.蒽环类抗生素的抗癌活性与DNA凝聚作用
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Redox pathway leading to the alkylation of DNA by the anthracycline, antitumor drugs adriamycin and daunomycin.导致蒽环类抗肿瘤药物阿霉素和柔红霉素使DNA烷基化的氧化还原途径。
J Med Chem. 1997 Apr 11;40(8):1276-86. doi: 10.1021/jm960835d.

引用本文的文献

1
Formation of alkali labile linkages in DNA by hedamycin and use of hedamycin as a probe of protein-DNA complexes.赫达霉素诱导DNA中碱不稳定键的形成及赫达霉素作为蛋白质-DNA复合物探针的应用
Nucleic Acids Res. 1982 Aug 11;10(15):4581-94. doi: 10.1093/nar/10.15.4581.
2
Comparative nuclear and cellular incorporation of daunorubicin, doxorubicin, carminomycin, marcellomycin, aclacinomycin A and AD 32 in daunorubicin-sensitive and -resistant Ehrlich ascites in vitro.柔红霉素、阿霉素、洋红霉素、马塞洛霉素、阿克拉霉素A和AD 32在体外对柔红霉素敏感和耐药的艾氏腹水瘤细胞核与细胞摄取的比较
J Cancer Res Clin Oncol. 1980;98(2):109-18. doi: 10.1007/BF00405955.
3
Anthracycline antitumour agents. A review of physicochemical, analytical and stability properties.
蒽环类抗肿瘤药物。物理化学、分析及稳定性性质综述。
Pharm Weekbl Sci. 1986 Apr 25;8(2):109-33. doi: 10.1007/BF02086146.
4
Template specificities of aclacinomycin B on the inhibition of DNA-dependent RNA synthesis in vitro.
Mol Cell Biochem. 1989 Oct 5;90(1):91-7. doi: 10.1007/BF00225224.
5
Menogaril, an anthracycline compound with a novel mechanism of action: cellular pharmacology.美诺加林,一种具有新型作用机制的蒽环类化合物:细胞药理学。
Jpn J Cancer Res. 1990 Aug;81(8):842-9. doi: 10.1111/j.1349-7006.1990.tb02654.x.