Synthesis, structures and the biological activity study on the metal complexes of 2-(4-aminophenyl)benzothiazole derivative
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T. Lu | Yi Lu | Taotao Yang | Yue Wang | Kewei Song | Q. Jin | Guowu Lin | Jiemei Song | Qing-Jie Huang | Jun-jie Zhou
[1] P. K. Basniwal,et al. 2-(4-aminophenyl) benzothiazole: a potent and selective pharmacophore with novel mechanistic action towards various tumour cell lines. , 2006, Mini reviews in medicinal chemistry.
[2] E. Sausville,et al. Anti-tumor drug candidate 2-(4-amino-3-methylphenyl)-5-fluorobenzothiazole induces single-strand breaks and DNA-protein cross-links in sensitive MCF-7 breast cancer cells , 2006, Cancer Chemotherapy and Pharmacology.
[3] Yan Jin,et al. DNA cleavage by copper-ATCUN complexes. Factors influencing cleavage mechanism and linearization of dsDNA. , 2005, Journal of the American Chemical Society.
[4] S. Mallik,et al. Inhibition of matrix metalloproteinase-9 by "multi-prong" surface binding groups. , 2005, Chemical communications.
[5] S. Mallik,et al. Two-prong inhibitors for human carbonic anhydrase II. , 2004, Journal of the American Chemical Society.
[6] S. Mallik,et al. Protein surface-assisted enhancement in the binding affinity of an inhibitor for recombinant human carbonic anhydrase-II. , 2004, Journal of the American Chemical Society.
[7] A. Monks,et al. The Experimental Antitumor Agents Phortress and Doxorubicin are Equiactive Against Human-Derived Breast Carcinoma Xenograft Models , 2004, Breast Cancer Research and Treatment.
[8] Ning Gan,et al. Oxidative DNA strand scission induced by a trinuclear copper(II) complex. , 2004, Inorganic chemistry.
[9] A. Westwell,et al. The development of the antitumour benzothiazole prodrug, Phortress, as a clinical candidate. , 2004, Current medicinal chemistry.
[10] G. Neelakanta,et al. Oxidative cleavage of DNA by a dipyridoquinoxaline copper(II) complex in the presence of ascorbic acid. , 2002, Journal of inorganic biochemistry.
[11] M. Stevens,et al. Antitumor benzothiazoles. 16. Synthesis and pharmaceutical properties of antitumor 2-(4-aminophenyl)benzothiazole amino acid prodrugs. , 2002, Journal of medicinal chemistry.
[12] M. E. Branum,et al. Double-strand DNA hydrolysis by dilanthanide complexes , 1999, JBIC Journal of Biological Inorganic Chemistry.
[13] E. Sausville,et al. Antitumor benzothiazoles. 8. Synthesis, metabolic formation, and biological properties of the C- and N-oxidation products of antitumor 2-(4-aminophenyl)benzothiazoles. , 1999, Journal of medicinal chemistry.
[14] Maria Cristina Burla,et al. SIR97: a new tool for crystal structure determination and refinement , 1999 .
[15] K. Paull,et al. 2-(4-Aminophenyl)benzothiazoles: novel agents with selective profiles of in vitro anti-tumour activity. , 1998, British Journal of Cancer.
[16] D. Davies,et al. Structural studies on bioactive compounds. 23. Synthesis of polyhydroxylated 2-phenylbenzothiazoles and a comparison of their cytotoxicities and pharmacological properties with genistein and quercetin. , 1994, Journal of medicinal chemistry.
[17] D. Crothers,et al. The carbohydrate domain of calicheamicin gamma I1 determines its sequence specificity for DNA cleavage. , 1991, Proceedings of the National Academy of Sciences of the United States of America.
[18] P. Yates,et al. Structural studies on benzothiazoles. Crystal and molecular structure of 5,6-dimethoxy-2-(4-methoxyphenyl-benzothiazole and molecular orbital calculations on related compounds. , 1991 .
[19] L. Povirk,et al. DNA double-strand breaks and alkali-labile bonds produced by bleomycin. , 1977, Nucleic acids research.
[20] J. Lepecq,et al. A fluorescent complex between ethidium bromide and nucleic acids. Physical-chemical characterization. , 1967, Journal of molecular biology.
[21] M. Waring,et al. Complex formation between ethidium bromide and nucleic acids. , 1965, Journal of molecular biology.
[22] J. Marmur. A procedure for the isolation of deoxyribonucleic acid from micro-organisms , 1961 .
[23] S. Rice,et al. A Further Examination of the Molecular Weight and Size of Desoxypentose Nucleic Acid , 1954 .