Ibandronate metal complexes: solution behavior and antiparasitic activity
暂无分享,去创建一个
Zhu-Hong Li | R. Docampo | D. Gambino | J. Maya | J. Torres | S. Rostán | Mauricio Moncada | L. Otero | Bruno Demoro | Claudio Olea Azar
[1] Ian H. Gilbert,et al. Anti-trypanosomatid drug discovery: an ongoing challenge and a continuing need , 2017, Nature Reviews Microbiology.
[2] L. Beneš,et al. Cerium(IV) phenylphosphonates and para-substituted phenylphosphonates: preparation and characterization , 2017, Journal of Inclusion Phenomena and Macrocyclic Chemistry.
[3] S. Adami,et al. The use of bisphosphonates in women: when to use and when to stop , 2015, Expert opinion on pharmacotherapy.
[4] M. Mizuguchi,et al. Protonation State and Hydration of Bisphosphonate Bound to Farnesyl Pyrophosphate Synthase. , 2015, Journal of medicinal chemistry.
[5] W. Goldeman,et al. Synthesis of N-methyl alkylaminomethane-1,1-diphosphonic acids and evaluation of their complex-formation abilities towards copper(II) , 2015 .
[6] B. Garat,et al. Effect of the metal ion on the anti T. cruzi activity and mechanism of action of 5-nitrofuryl-containing thiosemicarbazone metal complexes , 2014 .
[7] S. Strittmatter,et al. Overcoming Drug Development Bottlenecks With Repurposing: Old drugs learn new tricks , 2014, Nature Medicine.
[8] Stephen T. C. Wong,et al. Toward better drug repositioning: prioritizing and integrating existing methods into efficient pipelines. , 2014, Drug discovery today.
[9] L. Malpezzi,et al. Structural and thermal characterization of sodium ibandronate monohydrate , 2012, Journal of Thermal Analysis and Calorimetry.
[10] R. Faccio,et al. Bisphosphonate metal complexes as selective inhibitors of Trypanosoma cruzi farnesyl diphosphate synthase. , 2012, Dalton transactions.
[11] R. Russell,et al. Bisphosphonates: the first 40 years. , 2011, Bone.
[12] J. Castiglioni,et al. Risedronate metal complexes potentially active against Chagas disease. , 2010, Journal of inorganic biochemistry.
[13] C. Janiak,et al. Iron, copper and zinc ammonium-1-hydroxyalkylidene-diphosphonates with zero-, one- and two-dimensional covalent metal–ligand structures extended into three-dimensional supramolecular networks by charge-assisted hydrogen-bonding , 2010 .
[14] Rick L. Tarleton,et al. In Vitro and In Vivo High-Throughput Assays for the Testing of Anti-Trypanosoma cruzi Compounds , 2010, PLoS neglected tropical diseases.
[15] L. Tušek-Boz̆ić,et al. Spectroscopic and DFT study of 3-quinolyl-α-aminophosphonates , 2009 .
[16] Li‐Min Zheng,et al. A layered cobalt phosphonate exhibiting ferrimagnetism and slow magnetic relaxation , 2008 .
[17] R. Docampo,et al. The acidocalcisome as a target for chemotherapeutic agents in protozoan parasites. , 2008, Current pharmaceutical design.
[18] Li‐Min Zheng,et al. Ladder-like metal diphosphonates exhibiting field-induced magnetic transitions , 2007 .
[19] Li‐Min Zheng,et al. Layered cobalt(II) and nickel(II) diphosphonates showing canted antiferromagnetism and slow relaxation behavior. , 2007, Inorganic chemistry.
[20] M. Cassera,et al. A Solanesyl-diphosphate Synthase Localizes in Glycosomes of Trypanosoma cruzi* , 2006, Journal of Biological Chemistry.
[21] P. Kafarski,et al. Coordination abilities of piperyd-1-yl-methane-1,1-diphosphonic acids towards zinc(II), magnesium(II) and calcium(II): potentiometric and NMR studies. , 2006, Journal of inorganic biochemistry.
[22] Changwen Hu,et al. Transformation from a low-dimensional framework to a high-dimensional architecture based on different metal ions: syntheses, structures, and photoluminescences. , 2006, Inorganic chemistry.
[23] S. Knapp,et al. The molecular mechanism of nitrogen-containing bisphosphonates as antiosteoporosis drugs , 2006, Proceedings of the National Academy of Sciences of the United States of America.
[24] M. Motevalli,et al. Structural studies on new metal derivatives of osteoporosis therapeutic aminohydroxyalkylidenebisphosphonic acids with C4 and C6 aminoalkyl chains , 2006 .
[25] Wolfgang Jahnke,et al. Structural Basis for the Exceptional in vivo Efficacy of Bisphosphonate Drugs , 2006, ChemMedChem.
[26] V. Videnova-Adrabińska,et al. Supramolecular chemistry and complexation abilities of diphosphonic acids , 2005 .
[27] N. Redman-Furey,et al. Structural and analytical characterization of three hydrates and an anhydrate form of risedronate. , 2005, Journal of pharmaceutical sciences.
[28] Zhong‐Ming Sun,et al. Synthesis and structural characterization of three new manganese(II) diphosphonates with layered and double-chain architectures , 2005 .
[29] A. Valavanidis,et al. Comparative study of the formation of oxidative damage marker 8-hydroxy-2′-deoxyguanosine (8-OHdG) adduct from the nucleoside 2′-deoxyguanosine by transition metals and suspensions of particulate matter in relation to metal content and redox reactivity , 2005, Free radical research.
[30] E. Oldfield,et al. Inhibition of isoprene biosynthesis pathway enzymes by phosphonates, bisphosphonates, and diphosphates. , 2004, Journal of medicinal chemistry.
[31] A. Aboukaïs,et al. Formation of oligonuclear complexes between copper(II) and 1-hydroxyethane-1,1-diphosphonic acid , 2004 .
[32] J. Urbina,et al. Specific chemotherapy of Chagas disease: controversies and advances. , 2003, Trends in parasitology.
[33] P. Wardman,et al. Evidence for the Role of a Peroxidase Compound I-type Intermediate in the Oxidation of Glutathione, NADH, Ascorbate, and Dichlorofluorescin by Cytochrome c/H2O2 , 2003, Journal of Biological Chemistry.
[34] G. Bouet,et al. A comparison of the acidity and the complexing ability of (o-hydroxyphenyl) bis- and (o-hydroxyphenyl) mono-methylenephosphonic acids towards lanthanide(III) ions. , 2002, Talanta.
[35] H. Kozłowski,et al. Bisphosphonate chelating agents. Coordination ability of 1-phenyl-1-hydroxymethylene bisphosphonate towards Cu(2+) ions. , 2002, Journal of inorganic biochemistry.
[36] P. Kafarski,et al. Interactions of zinc(II), magnesium(II) and calcium(II) with aminomethane-1,1-diphosphonic acids in aqueous solutions , 2002 .
[37] E. Oldfield,et al. Bisphosphonates Are Potent Inhibitors of Trypanosoma cruzi Farnesyl Pyrophosphate Synthase* , 2001, The Journal of Biological Chemistry.
[38] R. Docampo,et al. Bisphosphonates as chemotherapeutic agents against trypanosomatid and apicomplexan parasites. , 2001, Current drug targets. Infectious disorders.
[39] P. Gans,et al. GLEE, a new computer program for glass electrode calibration. , 2000, Talanta.
[40] E. Oldfield,et al. Trypanosoma cruzi Contains Major Pyrophosphate Stores, and Its Growth in Vitro and in Vivo Is Blocked by Pyrophosphate Analogs* , 1999, The Journal of Biological Chemistry.
[41] P. Gans,et al. Hyperquad simulation and speciation (HySS): a utility program for the investigation of equilibria involving soluble and partially soluble species , 1999 .
[42] J. Bollinger,et al. Divalent cations speciation with three phosphonate ligands in the pH-range of natural waters. , 1997, Talanta.
[43] P. Gans,et al. Investigation of equilibria in solution. Determination of equilibrium constants with the HYPERQUAD suite of programs. , 1996, Talanta.
[44] P. Hermann,et al. Aminoalkylbis(phosphonates): Their Complexation Properties in Solution and in the Solid State , 2007 .
[45] H. Rilling. [16] Eukaryotic prenyltransferases , 1985 .