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2013

Journal Article

Alkyl substituted 2′-benzoylpyridine thiosemicarbazone chelators with potent and selective anti-neoplastic activity: novel ligands that limit methemoglobin formation

Stefani, Christian, Jansson, Patric J., Gutierrez, Elaine, Bernhardt, Paul V., Richardson, Des R. and Kalinowski, Danuta S. (2013). Alkyl substituted 2′-benzoylpyridine thiosemicarbazone chelators with potent and selective anti-neoplastic activity: novel ligands that limit methemoglobin formation. Journal of Medicinal Chemistry, 56 (1), 357-370. doi: 10.1021/jm301691s

Alkyl substituted 2′-benzoylpyridine thiosemicarbazone chelators with potent and selective anti-neoplastic activity: novel ligands that limit methemoglobin formation

2013

Journal Article

Template synthesis and X-ray structural characterization of nickel(II) and zinc(II) complexes of tetradentate SNNS ligands formed by condensation of phthalaldehyde with S-methyldithiocarbazate and N-4-methyl-3-thiosemicarbazide

Ali, Mohammad Akbar, Mirza, Aminul Huq, Mei, Chan Chin, Bernhardt, Paul V. and Karim, Mohammad Rezaul (2013). Template synthesis and X-ray structural characterization of nickel(II) and zinc(II) complexes of tetradentate SNNS ligands formed by condensation of phthalaldehyde with S-methyldithiocarbazate and N-4-methyl-3-thiosemicarbazide. Polyhedron, 49 (1), 277-283. doi: 10.1016/j.poly.2012.10.008

Template synthesis and X-ray structural characterization of nickel(II) and zinc(II) complexes of tetradentate SNNS ligands formed by condensation of phthalaldehyde with S-methyldithiocarbazate and N-4-methyl-3-thiosemicarbazide

2012

Journal Article

Low-potential amperometric enzyme biosensor for xanthine and hypoxanthine

Kalimuthu, Palraj, Leimkuhler, Silke and Bernhardt, Paul V. (2012). Low-potential amperometric enzyme biosensor for xanthine and hypoxanthine. Analytical Chemistry, 84 (23), 10359-10365. doi: 10.1021/ac3025027

Low-potential amperometric enzyme biosensor for xanthine and hypoxanthine

2012

Journal Article

Mixed-ligand nickel(II) and copper(II) complexes of tridentate ONS and NNS ligands derived from S-alkyldithiocarbazates with the saccharinate ion as a co-ligand

Ali, Mohammad Akbar, Mirza, Aminul Huq, Ting, Wong Yok, Hamid, Malai Haniti S. A., Bernhardt, Paul V. and Butcher, Ray J. (2012). Mixed-ligand nickel(II) and copper(II) complexes of tridentate ONS and NNS ligands derived from S-alkyldithiocarbazates with the saccharinate ion as a co-ligand. Polyhedron, 48 (1), 167-173. doi: 10.1016/j.poly.2012.08.069

Mixed-ligand nickel(II) and copper(II) complexes of tridentate ONS and NNS ligands derived from S-alkyldithiocarbazates with the saccharinate ion as a co-ligand

2012

Journal Article

Reversible rearrangements of Cu(II) cage complexes: solvent and anion influences

Bernhardt, Paul V., Font, Helena, Gallego, Carlos, Martinez, Manuel and Rodriguez, Carlos (2012). Reversible rearrangements of Cu(II) cage complexes: solvent and anion influences. Inorganic Chemistry, 51 (22), 12372-12379. doi: 10.1021/ic301696v

Reversible rearrangements of Cu(II) cage complexes: solvent and anion influences

2012

Journal Article

Synthesis, characterization and X-ray crystal structures of thiolate sulfur-bridged dimeric copper(II) complexes of the 2-aminoacetophenone Schiff base of S-methyldithiocarbazate

Akbar Ali, Mohammad, Mirza, Aminul Huq, Hamid, Malai Haniti S. A., Aminath, Nuzuhath and Bernhardt, Paul V. (2012). Synthesis, characterization and X-ray crystal structures of thiolate sulfur-bridged dimeric copper(II) complexes of the 2-aminoacetophenone Schiff base of S-methyldithiocarbazate. Polyhedron, 47 (1), 79-86. doi: 10.1016/j.poly.2012.08.024

Synthesis, characterization and X-ray crystal structures of thiolate sulfur-bridged dimeric copper(II) complexes of the 2-aminoacetophenone Schiff base of S-methyldithiocarbazate

2012

Journal Article

Catalytic electrochemistry of xanthine dehydrogenase

Kalimuthu, Palraj, Leimkuehler, Silke and Bernhardt, Paul V. (2012). Catalytic electrochemistry of xanthine dehydrogenase. Journal of Physical Chemistry B, 116 (38), 11600-11607. doi: 10.1021/jp307374z

Catalytic electrochemistry of xanthine dehydrogenase

2012

Journal Article

Novel second-generation Di-2-Pyridylketone Thiosemicarbazones show synergism with standard chemotherapeutics and demonstrate potent activity against lung cancer xenografts after oral and intravenous administration in vivo

Lovejoy, David B., Sharp, Danae M., Seebacher, Nicole, Obeidy, Peyman, Prichard, Thomas, Stefani, Christian, Basha, Maram T., Sharpe, Philip C., Jansson, Patric J., Kalinowski, Danuta S., Bernhardt, Paul V. and Richardson, Des R. (2012). Novel second-generation Di-2-Pyridylketone Thiosemicarbazones show synergism with standard chemotherapeutics and demonstrate potent activity against lung cancer xenografts after oral and intravenous administration in vivo. Journal of Medicinal Chemistry, 55 (16), 7230-7244. doi: 10.1021/jm300768u

Novel second-generation Di-2-Pyridylketone Thiosemicarbazones show synergism with standard chemotherapeutics and demonstrate potent activity against lung cancer xenografts after oral and intravenous administration in vivo

2012

Journal Article

Methemoglobin formation by triapine, di-2-pyridylketone-4,4-dimethyl-3- thiosemicarbazone (Dp44mT), and other anticancer thiosemicarbazones: identification of novel thiosemicarbazones and therapeutics that prevent this effect

Quach, Patricia, Gutierrez, Elaine, Basha, Maram Talal, Kalinowski, Danuta S., Sharpe, Philip C., Lovejoy, David B., Bernhardt, Paul V., Jansson, Patric J. and Richardson, Des R. (2012). Methemoglobin formation by triapine, di-2-pyridylketone-4,4-dimethyl-3- thiosemicarbazone (Dp44mT), and other anticancer thiosemicarbazones: identification of novel thiosemicarbazones and therapeutics that prevent this effect. Molecular Pharmacology, 82 (1), 105-114. doi: 10.1124/mol.112.078964

Methemoglobin formation by triapine, di-2-pyridylketone-4,4-dimethyl-3- thiosemicarbazone (Dp44mT), and other anticancer thiosemicarbazones: identification of novel thiosemicarbazones and therapeutics that prevent this effect

2012

Journal Article

Heterocyclic dithiocarbazate iron chelators: Fe coordination chemistry and biological activity

Basha, Maram T., Chartres, Jy D., Pantarat, Namfon, Ali, Mohammad Akbar, Mirza, Aminul Huq, Kalinowski, Danuta S., Richardson, Des R. and Bernhardt, Paul V. (2012). Heterocyclic dithiocarbazate iron chelators: Fe coordination chemistry and biological activity. Dalton Transactions, 41 (21), 6536-6548. doi: 10.1039/c2dt12387h

Heterocyclic dithiocarbazate iron chelators: Fe coordination chemistry and biological activity

2012

Journal Article

Copper redistribution in murine macrophages in response to Salmonella infection

Achard, Maud E. S., Stafford, Sian L., Bokil, Nilesh J., Chartres, Jy, Bernhardt, Paul V., Schembri, Mark A., Sweet, Matthew J. and McEwan, Alastair G. (2012). Copper redistribution in murine macrophages in response to Salmonella infection. Biochemical Journal, 444 (1), 51-57. doi: 10.1042/BJ20112180

Copper redistribution in murine macrophages in response to Salmonella infection

2012

Journal Article

Stereocontrolled Synthesis of the cis-Hydroxydecalin System: Towards Biologically Active 19-nor-Clerodanes

Mirzayans, Paul Malek, Pouwer, Rebecca H., Williams, Craig M. and Bernhardt, Paul V. (2012). Stereocontrolled Synthesis of the cis-Hydroxydecalin System: Towards Biologically Active 19-nor-Clerodanes. European Journal of Organic Chemistry, 8 (8), 1633-1638. doi: 10.1002/ejoc.201101807

Stereocontrolled Synthesis of the cis-Hydroxydecalin System: Towards Biologically Active 19-nor-Clerodanes

2012

Journal Article

Heronamycin A: A new benzothiazine ansamycin from an Australian marine-derived Streptomyces sp.

Raju, Ritesh, Piggott, Andrew M., Khalil, Zeinab, Bernhardt, Paul V. and Capon, Robert J. (2012). Heronamycin A: A new benzothiazine ansamycin from an Australian marine-derived Streptomyces sp.. Tetrahedron Letters, 53 (9), 1063-1065. doi: 10.1016/j.tetlet.2011.12.064

Heronamycin A: A new benzothiazine ansamycin from an Australian marine-derived Streptomyces sp.

2012

Journal Article

Crystal Structures of (3R,3aR,4S,7R,7aS)-3-(Allyloxy)hexahydro-4,7-epoxyisobenzofuran-1(3H)-one and (3S,3aR,4S,7R,7aS)-3-((E)-But-2-en-1-yloxy)hexahydro-4,7-epoxyisobenzofuran-1(3H)-one: Confirmation of NMR Predicted Stereocentre Geometry

Tarleton, Mark, Bernhardt, Paul V. and McCluskey, Adam (2012). Crystal Structures of (3R,3aR,4S,7R,7aS)-3-(Allyloxy)hexahydro-4,7-epoxyisobenzofuran-1(3H)-one and (3S,3aR,4S,7R,7aS)-3-((E)-But-2-en-1-yloxy)hexahydro-4,7-epoxyisobenzofuran-1(3H)-one: Confirmation of NMR Predicted Stereocentre Geometry. Journal of Chemical Crystallography, 42 (6), 639-644. doi: 10.1007/s10870-012-0275-z

Crystal Structures of (3R,3aR,4S,7R,7aS)-3-(Allyloxy)hexahydro-4,7-epoxyisobenzofuran-1(3H)-one and (3S,3aR,4S,7R,7aS)-3-((E)-But-2-en-1-yloxy)hexahydro-4,7-epoxyisobenzofuran-1(3H)-one: Confirmation of NMR Predicted Stereocentre Geometry

2012

Journal Article

A solid state study of keto-enol tautomerismin in three naphthaledene Schiff bases

Pierens, Gregory K., Venkatachalam, T. K., Bernhardt, Paul V., Riley, Mark J. and Reutens, David C. (2012). A solid state study of keto-enol tautomerismin in three naphthaledene Schiff bases. Australian Journal of Chemistry, 65 (5), 552-556. doi: 10.1071/CH12122

A solid state study of keto-enol tautomerismin in three naphthaledene Schiff bases

2012

Journal Article

Polymorphism in 3-Pyridylsydnone: Preparative and Structural Aspects

Bernhardt, Paul V., Kvaskoff, David, Veedu, Rakesh Naduvile and Wentrup, Curt (2012). Polymorphism in 3-Pyridylsydnone: Preparative and Structural Aspects. Australian Journal of Chemistry, 65 (4), 376-380. doi: 10.1071/CH12041

Polymorphism in 3-Pyridylsydnone: Preparative and Structural Aspects

2012

Journal Article

The role of Zn-OR and Zn-OH nucleophiles and the influence of para-substituents in the reactions of binuclear phosphatase mimetics

Daumann, Lena J., Dalle, Kristian E., Schenk, Gerhard, McGeary, Ross P., Bernhardt, Paul V., Ollis, David L. and Gahan, Lawrence R. (2012). The role of Zn-OR and Zn-OH nucleophiles and the influence of para-substituents in the reactions of binuclear phosphatase mimetics. Dalton Transactions, 41 (6), 1695-1708. doi: 10.1039/c1dt11187f

The role of Zn-OR and Zn-OH nucleophiles and the influence of para-substituents in the reactions of binuclear phosphatase mimetics

2012

Journal Article

Biologically active thiosemicarbazone Fe chelators and their reactions with ferrioxamine B and ferric EDTA; a kinetic study

Bernhardt, Paul V., Martínez, Manuel, Rodríguez, Carlos and Vazquez, Marta (2012). Biologically active thiosemicarbazone Fe chelators and their reactions with ferrioxamine B and ferric EDTA; a kinetic study. Dalton Transactions, 41 (7), 2122-2130. doi: 10.1039/C1DT11685A

Biologically active thiosemicarbazone Fe chelators and their reactions with ferrioxamine B and ferric EDTA; a kinetic study

2012

Journal Article

Reactivity of di-iodine toward thiol: Desulfuration reaction of 5-nitro-2-mercapto-benzimidazole upon reaction with di-iodine

Corban, G. J., Antoniadis, C. D., Hadjikakou, S. K., Kourkoumelis, N., Tyurin, V. Yu., Dolgano, A., Milaeva, E. R., Kubicki, M., Bernhardt, P. V., Tiekink, E. R. T., Skoulika, S. and Hadjiliadis, N. (2012). Reactivity of di-iodine toward thiol: Desulfuration reaction of 5-nitro-2-mercapto-benzimidazole upon reaction with di-iodine. Heteroatom Chemistry, 23 (5), 498-511. doi: 10.1002/hc.21042

Reactivity of di-iodine toward thiol: Desulfuration reaction of 5-nitro-2-mercapto-benzimidazole upon reaction with di-iodine

2012

Journal Article

Structures of 4-iminopyrido[1,2-a]pyrimidines, pyrido[1,2-a]pyrimidin-4-ones, pyridopyrimidinium olates, and thiazolo[3,2-a]pyrimidine analogues

Bernhardt, Paul V. and Wentrup, Curt (2012). Structures of 4-iminopyrido[1,2-a]pyrimidines, pyrido[1,2-a]pyrimidin-4-ones, pyridopyrimidinium olates, and thiazolo[3,2-a]pyrimidine analogues. Australian Journal of Chemistry, 65 (4), 371-375. doi: 10.1071/CH12040

Structures of 4-iminopyrido[1,2-a]pyrimidines, pyrido[1,2-a]pyrimidin-4-ones, pyridopyrimidinium olates, and thiazolo[3,2-a]pyrimidine analogues