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2007

Journal Article

Design of bioavailable derivatives of 12-(3-adamantan-1-yl-ureido)dodecanoic acid, a potent inhibitor of the soluble epoxide hydrolase

Kim, I., Nishi, I., Tsai, H., Bradford, T., Koda, Y., Watanabe, T., Morriseau, C., Blanchfield, J., Toth, I. and Hammock, B. (2007). Design of bioavailable derivatives of 12-(3-adamantan-1-yl-ureido)dodecanoic acid, a potent inhibitor of the soluble epoxide hydrolase. Bioorganic & Medicinal Chemistry, 15 (1), 312-323. doi: 10.1016/j.bmc.2006.09.057

Design of bioavailable derivatives of 12-(3-adamantan-1-yl-ureido)dodecanoic acid, a potent inhibitor of the soluble epoxide hydrolase

2006

Journal Article

Particulate systems as adjuvants and carriers for peptide and protein antigens

Liang, M T, Davies, N M, Blanchfield, J T and Toth, I (2006). Particulate systems as adjuvants and carriers for peptide and protein antigens. Current Drug Delivery, 3 (4), 379-388. doi: 10.2174/156720106778559029

Particulate systems as adjuvants and carriers for peptide and protein antigens

2006

Journal Article

Synthesis of a library of polycationic lipid core dendrimers and their evaluation in the delivery of an oligonucleotide with hVEGF inhibition

Parekh, H. S., Marano, R. J., Rakoczy, E. P., Blanchfield, J. and Toth, I. (2006). Synthesis of a library of polycationic lipid core dendrimers and their evaluation in the delivery of an oligonucleotide with hVEGF inhibition. Bioorganic & Medicinal Chemistry, 14 (14), 4775-4780. doi: 10.1016/j.bmc.2006.03.029

Synthesis of a library of polycationic lipid core dendrimers and their evaluation in the delivery of an oligonucleotide with hVEGF inhibition

2006

Journal Article

Epidermal penetration of a therapeutic peptide by lipid conjugation; Stereo-selective peptide availability of a topical diastereomeric lipopeptide

Caccetta, R., Blanchfield, J. T., Harrison, J., Toth, I. and Benson, H. A. E. (2006). Epidermal penetration of a therapeutic peptide by lipid conjugation; Stereo-selective peptide availability of a topical diastereomeric lipopeptide. International Journal of Peptide Research and Therapeutics, 12 (3), 327-333. doi: 10.1007/s10989-006-9024-5

Epidermal penetration of a therapeutic peptide by lipid conjugation; Stereo-selective peptide availability of a topical diastereomeric lipopeptide

2006

Journal Article

Investigation of the route of absorption of lipid and sugar modified leu-enkephalin analogues and their enzymatic stability using the Caco-2 cell monolayer system

Wu, S., Christopher, C., Koda, Y., Blanchfield, J. T. and Toth, I. (2006). Investigation of the route of absorption of lipid and sugar modified leu-enkephalin analogues and their enzymatic stability using the Caco-2 cell monolayer system. Medicinal Chemistry, 2 (2), 203-211. doi: 10.2174/157340606776056205

Investigation of the route of absorption of lipid and sugar modified leu-enkephalin analogues and their enzymatic stability using the Caco-2 cell monolayer system

2005

Journal Article

Chemo-enzymatic synthesis of a trisaccharide-linked peptide aimed at improved drug-delivery

Johnstone, K. D., Dieckelmann, M., Jennings, M. P., Toth, I. and Blanchfield, J. T. (2005). Chemo-enzymatic synthesis of a trisaccharide-linked peptide aimed at improved drug-delivery. Current Drug Delivery, 2 (3), 215-222. doi: 10.2174/1567201054367977

Chemo-enzymatic synthesis of a trisaccharide-linked peptide aimed at improved drug-delivery

2005

Journal Article

The stability of lipidic analogues of GnRH in plasma and kidney preparations: the stereoselective release of the parent peptide

Blanchfield, J. T., Lew, R. A., Smith, A. I. and Toth, I. (2005). The stability of lipidic analogues of GnRH in plasma and kidney preparations: the stereoselective release of the parent peptide. Bioorganic & Medicinal Chemistry Letters, 15 (6), 1609-1612. doi: 10.1016/j.bmcl.2005.01.069

The stability of lipidic analogues of GnRH in plasma and kidney preparations: the stereoselective release of the parent peptide

2004

Journal Article

Micellar aggregation and membrane partitioning of bile salts, fatty acids, sodium dodecyl sulfate, and sugar-conjugated fatty acids: correlation with hemolytic potency and implications for drug delivery

Ross, Benjamin P., Braddy, April C., McGeary, Ross P., Blanchfield, Joanne T., Prokai, Laszlo and Toth, Istvan (2004). Micellar aggregation and membrane partitioning of bile salts, fatty acids, sodium dodecyl sulfate, and sugar-conjugated fatty acids: correlation with hemolytic potency and implications for drug delivery. Molecular Pharmaceutics, 1 (3), 233-245. doi: 10.1021/mp049964d

Micellar aggregation and membrane partitioning of bile salts, fatty acids, sodium dodecyl sulfate, and sugar-conjugated fatty acids: correlation with hemolytic potency and implications for drug delivery

2004

Journal Article

Permeability studies of alkylamides and caffeic acid conjugates from echinacea using a Caco-2 cell monolayer model

Matthias, A., Blanchfield, J. T., Penman, K. G., Toth, I., Lang, C. S., De Voss, J. J. and Lehmann, R. P. (2004). Permeability studies of alkylamides and caffeic acid conjugates from echinacea using a Caco-2 cell monolayer model. Journal of Clinical Pharmacy And Therapeutics, 29 (1), 7-13. doi: 10.1046/j.1365-2710.2003.00530.x

Permeability studies of alkylamides and caffeic acid conjugates from echinacea using a Caco-2 cell monolayer model

2004

Journal Article

Lipid, sugar and liposaccharide based delivery systems 2

Blanchfield, J. and Toth, I. (2004). Lipid, sugar and liposaccharide based delivery systems 2. Current Medicinal Chemistry, 11 (17), 2375-2382. doi: 10.2174/0929867043364621

Lipid, sugar and liposaccharide based delivery systems 2

2004

Journal Article

Mucosal immunization: Adjuvants and delivery systems

Moyle, P.M., McGeary, R. P., Blanchfield, J. T. and Toth, I. (2004). Mucosal immunization: Adjuvants and delivery systems. Current Drug Delivery, 1 (4), 385-396. doi: 10.2174/1567201043334588

Mucosal immunization: Adjuvants and delivery systems

2004

Journal Article

Concerning the proposed structure of (+)-laurobtusol: Spectral discrepancies with synthetic, racemic Stereoisomers

Blanchfield, Joanne T., Chow, Sharon, Bernhardt, Paul V., Kennard, Colin H. L. and Kitching, William (2004). Concerning the proposed structure of (+)-laurobtusol: Spectral discrepancies with synthetic, racemic Stereoisomers. Australian Journal of Chemistry, 57 (7), 673-676. doi: 10.1071/CH04047

Concerning the proposed structure of (+)-laurobtusol: Spectral discrepancies with synthetic, racemic Stereoisomers

2004

Journal Article

Boric acid catalyzed chemoselective esterification of alpha-hydroxycarboxylic acids

Houston, T. A., Wilkinson, B. L. and Blanchfield, J. T. (2004). Boric acid catalyzed chemoselective esterification of alpha-hydroxycarboxylic acids. Organic Letters, 6 (5), 679-681. doi: 10.1021/ol036123g

Boric acid catalyzed chemoselective esterification of alpha-hydroxycarboxylic acids

2003

Journal Article

Back to (non)-Basics: Recent developments in neutral and charge-balanced glycosidase inhibitors

Houston, T. A. and Blanchfield, J. T. (2003). Back to (non)-Basics: Recent developments in neutral and charge-balanced glycosidase inhibitors. Mini Reviews in Medicinal Chemistry, 3 (7), 669-678. doi: 10.2174/1389557033487827

Back to (non)-Basics: Recent developments in neutral and charge-balanced glycosidase inhibitors

2003

Journal Article

Stability of multielectron bubbles against single-electron split-off

Silvera, I. F., Blanchfield, J. and Tempere, J. (2003). Stability of multielectron bubbles against single-electron split-off. Physica Status Solidi (B) Basic Research, 237 (1), 274-279. doi: 10.1002/pssb.200301792

Stability of multielectron bubbles against single-electron split-off

2003

Journal Article

Synthesis, structure elucidation, in vitro biological activity, toxicity, and Caco-2 cell permeability of lipophilic analogues of α-conotoxin MII

Blanchfield, J. T., Dutton, J. T., Hogg, R. C., Gallagher, O. P., Craik, D. J., Jones, A., Adams, D. J., Lewis, R. J., Alewood, P. F. and Toth, I. (2003). Synthesis, structure elucidation, in vitro biological activity, toxicity, and Caco-2 cell permeability of lipophilic analogues of α-conotoxin MII. Journal of Medicinal Chemistry, 46 (7), 1266-1272. doi: 10.1021/jm020426j

Synthesis, structure elucidation, in vitro biological activity, toxicity, and Caco-2 cell permeability of lipophilic analogues of α-conotoxin MII

2003

Journal Article

Characterisation of alkaloids from some Australian Stephania (Menispermaceae) species

Blanchfield, J. T., Sands, D. P. A., Kennard, C. H. L., Byriel, K. A. and Kitching, W. (2003). Characterisation of alkaloids from some Australian Stephania (Menispermaceae) species. Phytochemistry, 63 (6), 711-720. doi: 10.1016/S0031-9422(03)00240-1

Characterisation of alkaloids from some Australian Stephania (Menispermaceae) species

2001

Journal Article

The synthesis and structure of an n-terminal dodecanoic acid conjugate of a-conotoxin MII

Blanchfield, Joanne T., Dutton, Julie T., Hogg, R. C., Craik, D. J., Adams, D. J., Lewis, R. J., Alewood, P. and Toth, I. (2001). The synthesis and structure of an n-terminal dodecanoic acid conjugate of a-conotoxin MII. Letters in Peptide Science, 8 (3-5), 235-239. doi: 10.1023/A:1016577832311

The synthesis and structure of an n-terminal dodecanoic acid conjugate of a-conotoxin MII

2000

Journal Article

Three unusal reactions mediate carbapenem and carbapenam biosynthesis

Rongfeng, L., Stapon, A., Blanchfield, J. T. and Townsend, C. A. (2000). Three unusal reactions mediate carbapenem and carbapenam biosynthesis. Journal of the American Chemical Society, 122 (38), 9296-9297. doi: 10.1021/ja0017231

Three unusal reactions mediate carbapenem and carbapenam biosynthesis

1994

Journal Article

Caloundrin-B and Funiculatin-A - New Polypropionates From Siphonariid Limpets

Blanchfield, JT, Brecknell, DJ, Brereton, IM, Garson, MJ and Jones, DD (1994). Caloundrin-B and Funiculatin-A - New Polypropionates From Siphonariid Limpets. Australian Journal of Chemistry, 47 (12), 2255-2269. doi: 10.1071/CH9942255

Caloundrin-B and Funiculatin-A - New Polypropionates From Siphonariid Limpets