Antitumor copper(II) complexes with hydroxyanthraquinones and N,N-heterocyclic ligands.
暂无分享,去创建一个
Z. Molphy | V. McKee | A. Kellett | A. Bortoluzzi | E. Pereira-Maia | A. M. da Costa Ferreira | B. Rodrigues | Rodrigo B. Fazzi | Ívina P. de Souza | A. C. de Melo | Simon Poole | Simon Poole
[1] A. Casini,et al. Connecting copper and cancer: from transition metal signalling to metalloplasia , 2021, Nature Reviews Cancer.
[2] L. Goulart,et al. In vitro and in vivo antitumoral activity of a ternary copper (II) complex. , 2020, Biochemical and biophysical research communications.
[3] S. Elledge,et al. The primary mechanism of cytotoxicity of the chemotherapeutic agent CX-5461 is topoisomerase II poisoning , 2020, Proceedings of the National Academy of Sciences.
[4] C. Slator,et al. CHAPTER 4. Recent Advances in Anticancer Copper Compounds , 2019, Metal-based Anticancer Agents.
[5] Abdulaziz A. Alkhedhairy,et al. Copper(II) complexes as potential anticancer and Nonsteroidal anti-inflammatory agents: In vitro and in vivo studies , 2019, Scientific Reports.
[6] N. Margiotta,et al. Cytotoxic phenanthroline derivatives alter metallostasis and redox homeostasis in neuroblastoma cells , 2018, Oncotarget.
[7] K. Hevener,et al. Recent developments in topoisomerase-targeted cancer chemotherapy , 2018, Acta pharmaceutica Sinica. B.
[8] Katia G. Samper,et al. Revisiting the thiosemicarbazonecopper(II) reaction with glutathione. Activity against colorectal carcinoma cell lines. , 2018, Journal of inorganic biochemistry.
[9] T. Brown,et al. Di-copper metallodrugs promote NCI-60 chemotherapy via singlet oxygen and superoxide production with tandem TA/TA and AT/AT oligonucleotide discrimination , 2018, Nucleic acids research.
[10] F. Pavan,et al. Novel copper(II) complexes with hydrazides and heterocyclic bases: Synthesis, structure and biological studies. , 2017, Journal of inorganic biochemistry.
[11] N. Tounsi,et al. Progress in Copper Complexes as Anticancer Agents , 2017 .
[12] M. E. Bravo-Gómez,et al. Genotoxic assessment of the copper chelated compounds Casiopeinas: Clues about their mechanisms of action. , 2017, Journal of inorganic biochemistry.
[13] H. Terenzi,et al. Impact of metal coordination on the antibiotic and non-antibiotic activities of tetracycline-based drugs , 2016 .
[14] Vladimír Lukes,et al. Study of natural anthraquinone colorants by EPR and UV/vis spectroscopy , 2016 .
[15] F. Pavan,et al. Synthesis, cytotoxic and antitubercular activities of copper(II) complexes with heterocyclic bases and 3-hydroxypicolinic acid , 2016 .
[16] C. Slator,et al. DNA oxidation profiles of copper phenanthrene chemical nucleases , 2015, Front. Chem..
[17] A. Riyasdeen,et al. Mixed ligand copper(II) complexes of 2,9-dimethyl-1,10-phenanthroline: tridentate 3N primary ligands determine DNA binding and cleavage and cytotoxicity. , 2014, Journal of inorganic biochemistry.
[18] D. Chandran,et al. Copper phenanthrene oxidative chemical nucleases. , 2014, Inorganic chemistry.
[19] A. Bortoluzzi,et al. Correlation between DNA interactions and cytotoxic activity of four new ternary compounds of copper(II) with N-donor heterocyclic ligands. , 2014, Journal of inorganic biochemistry.
[20] S. Avnet,et al. The natural compound Alizarin as an osteotropic drug for the treatment of bone tumors , 2012, Journal of orthopaedic research : official publication of the Orthopaedic Research Society.
[21] X. Xuan,et al. Theoretical study of molecular structure and vibrational spectra of 1,4-dihydroxyanthraquinone. , 2011, Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy.
[22] G. Jin,et al. Synthesis and antiproliferative activity of 1,4-bis(dimethylamino)-9,10-anthraquinone derivatives against P388 mouse leukemic tumor cells , 2011, Archives of pharmacal research.
[23] A. Neves,et al. Two new ternary complexes of copper(II) with tetracycline or doxycycline and 1,10-phenanthroline and their potential as antitumoral: cytotoxicity and DNA cleavage. , 2011, Inorganic chemistry.
[24] D. Newton,et al. A copper chelate of thiosemicarbazone NSC 689534 induces oxidative/ER stress and inhibits tumor growth in vitro and in vivo. , 2011, Free radical biology & medicine.
[25] M. E. Bravo-Gómez,et al. Copper compounds in cancer chemotherapy. , 2010, Current medicinal chemistry.
[26] Li‐Min Liu,et al. Cytotoxicity of the traditional chinese medicine (TCM) plumbagin in its copper chemistry. , 2009, Dalton transactions.
[27] Partha Sarathi Guin,et al. Studies on the formation of a complex of Cu(II) with sodium 1,4-dihydroxy-9,10-anthraquinone-2-sulphonate - an analogue of the core unit of anthracycline anticancer drugs and its interaction with calf thymus DNA. , 2009, Journal of inorganic biochemistry.
[28] P. Ruggerone,et al. Copper-1,10-phenanthroline complexes binding to DNA: structural predictions from molecular simulations. , 2009, Journal of Physical Chemistry B.
[29] S. Moro,et al. DNA topoisomerase II structures and anthracycline activity: insights into ternary complex formation. , 2007, Current pharmaceutical design.
[30] L. Ruiz-Azuara,et al. Induction of oxidative damage by copper-based antineoplastic drugs (Casiopeínas®) , 2007, Cancer Chemotherapy and Pharmacology.
[31] Arthur Schweiger,et al. EasySpin, a comprehensive software package for spectral simulation and analysis in EPR. , 2006, Journal of magnetic resonance.
[32] S. Moro,et al. Interaction model for anthracycline activity against DNA topoisomerase II. , 2004, Biochemistry.
[33] A. De Vizcaya-Ruiz,et al. Hematotoxicity response in rats by the novel copper-based anticancer agent: casiopeina II. , 2003, Toxicology.
[34] L. Messori,et al. Structure of a terbium(III)-quinizarine complex: the first crystallographic model for metalloanthracyclines. , 2003, Inorganic chemistry.
[35] Laurence H. Hurley,et al. DNA and its associated processes as targets for cancer therapy , 2002, Nature Reviews Cancer.
[36] H. Wang,et al. Antitumor activity of the Cu(II)-mitoxantrone complex and its interaction with deoxyribonucleic acid. , 1996, Journal of inorganic biochemistry.
[37] T. B. Nasrallah,et al. Is a hydrogen bond responsible for the optical properties of some dihydroxyanthraquinones: Quinizarin and anthraflavic? , 1995 .
[38] R. Peacock,et al. Electronic absorption spectra of the iron(II) complexes of 2,2'-bipyridine, 2,2'-bipyrimidine, 1,10-phenanthroline, and 2,2':6',2''-terpyridine and their reduction products , 1992 .
[39] D. Sigman,et al. Chemical nucleases. , 1990, Biochemistry.
[40] T. Larsen,et al. Nuclease activity of 1,10-phenanthroline―copper: kinetic mechanism , 1989 .
[41] R. O. Day,et al. Structural model for the binding of iron by anthracycline drugs , 1989 .
[42] P. Dutta,et al. Infrared and resonance Raman spectroscopic studies of 1-hydroxy-9,10-anthraquinone and its metal complexes , 1987 .
[43] A. W. Addison,et al. Spectroscopic and redox studies of some copper(II) complexes with biomimetic donor atoms: implications for protein copper centres , 1979 .
[44] R. A. Walker. Metal complexes of l-hydroxy-9,10-anthraquinone—I: Infrared spectra (4000–350 cm−1) of complexes formed with divalent cations , 1971 .