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2016

Journal Article

Discovery and structure-activity relationships of a highly selective butyrylcholinesterase inhibitor by Structure-based virtual screening

Dighe, Satish N., Deora, Girdhar Singh, De la Mora, Eugenio, Nachon, Florian, Chan, Stephen, Parat, Marie-Odile, Brazzolotto, Xavier and Ross, Benjamin P. (2016). Discovery and structure-activity relationships of a highly selective butyrylcholinesterase inhibitor by Structure-based virtual screening. Journal of Medicinal Chemistry, 59 (16), 7683-7689. doi: 10.1021/acs.jmedchem.6b00356

Discovery and structure-activity relationships of a highly selective butyrylcholinesterase inhibitor by Structure-based virtual screening

2016

Journal Article

Metal chelation, radical scavenging and inhibition of Aβ42 fibrillation by food constituents in relation to Alzheimer's disease

Chan, Stephen, Kantham, Srinivas, Rao, Venkatesan M., Palanivelu, Manoj Kumar, Pham, Hoang L., Shaw, P. Nicholas, McGeary, Ross P. and Ross, Benjamin P. (2016). Metal chelation, radical scavenging and inhibition of Aβ42 fibrillation by food constituents in relation to Alzheimer's disease. Food Chemistry, 199, 185-194. doi: 10.1016/j.foodchem.2015.11.118

Metal chelation, radical scavenging and inhibition of Aβ42 fibrillation by food constituents in relation to Alzheimer's disease

2014

Journal Article

'Click' assembly of glycoclusters and discovery of a trehalose analogue that retards A(beta)40 aggregation and inhibits A(beta)40-induced neurotoxicity

Rajaram, Hemalatha, Palanivelu, Manoj Kumar, Arumugam, Thiruma V., Rao, Venkatesan M., Shaw, P. Nicholas, McGeary, Ross P. and Ross, Benjamin P. (2014). 'Click' assembly of glycoclusters and discovery of a trehalose analogue that retards A(beta)40 aggregation and inhibits A(beta)40-induced neurotoxicity. Bioorganic and Medicinal Chemistry Letters, 24 (18), 4523-4528. doi: 10.1016/j.bmcl.2014.07.077

'Click' assembly of glycoclusters and discovery of a trehalose analogue that retards A(beta)40 aggregation and inhibits A(beta)40-induced neurotoxicity

2013

Journal Article

Cyclodextrin-crosslinked poly(acrylic acid): adhesion and controlled release of diflunisal and fluconazole from solid dosage forms

Kutyla, Marguerite J., Boehm, Michael W., Stokes, Jason R., Shaw, P. Nicholas, Davies, Nigel M., McGeary, Ross P., Tuke, Jonathan and Ross, Benjamin P. (2013). Cyclodextrin-crosslinked poly(acrylic acid): adhesion and controlled release of diflunisal and fluconazole from solid dosage forms. AAPS PharmSciTech, 14 (1), 301-311. doi: 10.1208/s12249-012-9903-3

Cyclodextrin-crosslinked poly(acrylic acid): adhesion and controlled release of diflunisal and fluconazole from solid dosage forms

2013

Journal Article

Cyclodextrin-crosslinked poly(acrylic acid): synthesis, physicochemical characterization and controlled release of diflunisal and fluconazole from hydrogels

Marguerite J. Kutyla, Lynette K. Lambert, Nigel M. Davies, Ross P. McGeary, P. Nicholas Shaw and Benjamin P. Ross (2013). Cyclodextrin-crosslinked poly(acrylic acid): synthesis, physicochemical characterization and controlled release of diflunisal and fluconazole from hydrogels. International Journal of Pharmaceutics, 444 (1-2), 175-184. doi: 10.1016/j.ijpharm.2013.01.005

Cyclodextrin-crosslinked poly(acrylic acid): synthesis, physicochemical characterization and controlled release of diflunisal and fluconazole from hydrogels

2012

Journal Article

Enzyme-responsive controlled release of covalently bound prodrug from functional mesoporous silica nanospheres

Popat, Amirali, Ross, Benjamin P., Liu, Jian, Jambhrunkar, Siddharth, Kleitz, Freddy and Qiao, Shi Zhang (2012). Enzyme-responsive controlled release of covalently bound prodrug from functional mesoporous silica nanospheres. Angewandte Chemie International, 51 (50), 12486-12489. doi: 10.1002/anie.201206416

Enzyme-responsive controlled release of covalently bound prodrug from functional mesoporous silica nanospheres

2012

Journal Article

2-Mercaptobenzothiazole and its derivatives: Syntheses, reactions and applications

Wu, Feng-Ling, Hussein, Waleed M., Ross, Benjamin P. and McGeary, Ross P. (2012). 2-Mercaptobenzothiazole and its derivatives: Syntheses, reactions and applications. Current Organic Chemistry, 16 (13), 1555-1580. doi: 10.2174/138527212800840964

2-Mercaptobenzothiazole and its derivatives: Syntheses, reactions and applications

2011

Journal Article

Phytochemical study of Fagraea spp. uncovers a new terpene alkaloid with anti-inflammatory properties

Suciati, Lambert, Lynette K., Ross, Benjamin P., Deseo, Myrna A. and Garson, Mary J. (2011). Phytochemical study of Fagraea spp. uncovers a new terpene alkaloid with anti-inflammatory properties. Australian Journal of Chemistry, 64 (4), 489-494. doi: 10.1071/CH10421

Phytochemical study of Fagraea spp. uncovers a new terpene alkaloid with anti-inflammatory properties

2010

Journal Article

New methodology for the conversion of epoxides to alkenes

Wu, Feng-Ling, Ross, Benjamin P. and McGeary, Ross P. (2010). New methodology for the conversion of epoxides to alkenes. European Journal of Organic Chemistry, 2010 (10), 1989-1998. doi: 10.1002/ejoc.200901264

New methodology for the conversion of epoxides to alkenes

2009

Journal Article

An 'inside-out' approach to suramin analogues

McGeary, Ross P., Bennett, Andrew J., Tran, Quoc B., Prins, Johannes and Ross, Benjamin P. (2009). An 'inside-out' approach to suramin analogues. Tetrahedron, 65 (20), 3990-3997. doi: 10.1016/j.tet.2009.03.033

An 'inside-out' approach to suramin analogues

2009

Journal Article

Synthesis of nickel-chelating fluorinated lipids for protein monolayer crystallizations

Hussein, Waleed M., Ross, Benjamin P., Landsberg, Michael J., Levy, Daniel, Hankamer, Ben and McGeary, Ross P. (2009). Synthesis of nickel-chelating fluorinated lipids for protein monolayer crystallizations. Journal of Organic Chemistry, 74 (4), 1473-1479. doi: 10.1021/jo802651p

Synthesis of nickel-chelating fluorinated lipids for protein monolayer crystallizations

2009

Journal Article

Synthesis of cationic derivatives of Quil A and the preparation of cationic immune-stimulating complexes (ISCOMs)

Pham, Hoang L., Ross, Benjamin P., McGeary, Ross P., Shaw, P. Nicholas and Davies, Nigel M. (2009). Synthesis of cationic derivatives of Quil A and the preparation of cationic immune-stimulating complexes (ISCOMs). International Journal of Pharmaceutics, 376 (1-2), 123-133. doi: 10.1016/j.ijpharm.2009.04.011

Synthesis of cationic derivatives of Quil A and the preparation of cationic immune-stimulating complexes (ISCOMs)

2009

Journal Article

Synthetic approaches to functionalized lipids for protein monolayer crystallizations

Hussein. Waleed M., Ross, Benjamin P., Landsberg, M. J., Hankamer, B and McGeary, Ross P. (2009). Synthetic approaches to functionalized lipids for protein monolayer crystallizations. Current Organic Chemistry, 13 (14), 1378-1405. doi: 10.2174/138527209789055081

Synthetic approaches to functionalized lipids for protein monolayer crystallizations

2009

Journal Article

Efficient manual Fmoc solid-phase synthesis of the N-Terminal segment of surfactant protein B (SP-B1-25)

Ramli, Suria, Gentle, Ian R. and Ross, Benjamin P. (2009). Efficient manual Fmoc solid-phase synthesis of the N-Terminal segment of surfactant protein B (SP-B1-25). Protein and Peptide Letters, 16 (7), 810-814. doi: 10.2174/092986609788681706

Efficient manual Fmoc solid-phase synthesis of the N-Terminal segment of surfactant protein B (SP-B1-25)

2008

Journal Article

Suramin: Clinical uses and structure-activity relationships

McGeary, Ross P., Bennett, Andrew J., Tran, Quoc B., Cosgrove, Kelly L. and Ross, Benjamin P. (2008). Suramin: Clinical uses and structure-activity relationships. Mini Reviews in Medicinal Chemistry, 8 (13), 1384-1394. doi: 10.2174/138955708786369573

Suramin: Clinical uses and structure-activity relationships

2008

Journal Article

N-1-(4,4-dimethyl-2,6-dioxocyclohex-1-ylidene)ethyl (N-Dde) Lipoamino Acids

Ross, Benjamin P., Falconer, Robert A. and Toth,, Istvan (2008). N-1-(4,4-dimethyl-2,6-dioxocyclohex-1-ylidene)ethyl (N-Dde) Lipoamino Acids. Molbank, 2008: M566 (2), M566. doi: 10.3390/M566

N-1-(4,4-dimethyl-2,6-dioxocyclohex-1-ylidene)ethyl (N-Dde) Lipoamino Acids

2007

Journal Article

Caco-2 cell permeability and stability of two D-glucopyranuronamide conjugates of thyrotropin-releasing hormone

Wessling, Susanne T., Ross, Benjamin P., Koda, Yasuko, Blanchfield, Joanne T. and Toth, Istvan (2007). Caco-2 cell permeability and stability of two D-glucopyranuronamide conjugates of thyrotropin-releasing hormone. Bioorganic & Medicinal Chemistry, 15 (14), 4946-4950. doi: 10.1016/j.bmc.2007.04.042

Caco-2 cell permeability and stability of two D-glucopyranuronamide conjugates of thyrotropin-releasing hormone

2006

Journal Article

Rhodamine B pentyl ester and its methyl, ethyl, propyl, and butyl homologues

Ross, Justin A., Ross, Benjamin P., Cosgrove, Kelly L., Rubinsztein-Dunlop, Halina and McGeary, Ross P. (2006). Rhodamine B pentyl ester and its methyl, ethyl, propyl, and butyl homologues. Molbank, 2006: M515 (6) M515, 1-4. doi: 10.3390/M515

Rhodamine B pentyl ester and its methyl, ethyl, propyl, and butyl homologues

2006

Journal Article

Saponins from Quillaja saponaria Molina: Isolation, Characterization and Ability to Form Immuno Stimulatory Complexes (ISCOMs)

Pham, H. L., Ross, B. P., McGeary, R. P., Shaw, P. N., Hewavitharana, A. K. and Davies, N. M. (2006). Saponins from Quillaja saponaria Molina: Isolation, Characterization and Ability to Form Immuno Stimulatory Complexes (ISCOMs). Current Drug Delivery, 3 (4), 389-397. doi: 10.2174/156720106778559092

Saponins from Quillaja saponaria Molina: Isolation, Characterization and Ability to Form Immuno Stimulatory Complexes (ISCOMs)

2006

Journal Article

Facile synthesis of rhodamine esters using acetyl chloride in alcohol solution

Ross, J. A., Ross, B. P., Rubinsztein-Dunlop, H. and McGeary, R. P. (2006). Facile synthesis of rhodamine esters using acetyl chloride in alcohol solution. Synthetic Communications, 36 (12), 1745-1750. doi: 10.1080/00397910600616818

Facile synthesis of rhodamine esters using acetyl chloride in alcohol solution