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2006

Conference Publication

Defining the ligand binding site on the human C5a receptor

Monk, Peter N., Higginbottom, Adrian, Madala, Praveen K., Tyndall, Joel D. A., Stoermer, Martin and Fairlie, David P. (2006). Defining the ligand binding site on the human C5a receptor. The 231st ACS National Meeting, Atlanta, GA, U.S.A., 26-30 March 2006. Washington, D.C.: American Chemical Society.

Defining the ligand binding site on the human C5a receptor

2005

Conference Publication

Development of a catalytically active recombinant West Nile NS3 protease and the identification of key enzyme-substrate interactions by site-directed mutagenesis

Chappell, K. J., Stoermer, M. J., Fairlie, D. and Young, P. R. (2005). Development of a catalytically active recombinant West Nile NS3 protease and the identification of key enzyme-substrate interactions by site-directed mutagenesis. 30th Lorne Conference on Protein Structure & Function, Lorne, 6-10 Feb, 2005.

Development of a catalytically active recombinant West Nile NS3 protease and the identification of key enzyme-substrate interactions by site-directed mutagenesis

2005

Conference Publication

Development of a catalytically active recombinant West Nile virus NS3 protease and the identification of key enzyme-substrate and enzyme-cofactor interactions by site-directed mutagenesis

Chappell, K. J., Stoermer, M. J., Fairlie, D. and Young, P. R. (2005). Development of a catalytically active recombinant West Nile virus NS3 protease and the identification of key enzyme-substrate and enzyme-cofactor interactions by site-directed mutagenesis. 3rd Australian Virology Group Meeting, Phillip Island, Vic., 9-12 Dec, 2005.

Development of a catalytically active recombinant West Nile virus NS3 protease and the identification of key enzyme-substrate and enzyme-cofactor interactions by site-directed mutagenesis

2005

Conference Publication

Development of antiviral drugs targeting the flaviviruses fusion mechanism

Kampmann, T., Yennamalli, R., Stoermer, M., Kobe, B. and Young, P. (2005). Development of antiviral drugs targeting the flaviviruses fusion mechanism. 30th FEBS Congress - 9th IUBMB Conference, Budapest, Hungary, 2-7tJuly 2005. Oxford, England: Blackwell Publishing. doi: 10.1111/j.1742-4658.2005.4739_15.x

Development of antiviral drugs targeting the flaviviruses fusion mechanism

2005

Conference Publication

Discovery of antiviral inhibitors targeting the fusion mechanism of the flavivirus family members Dengue, Kunjin and Yellow fever

Kampmann, T., Yennamalli Madhava R, R., Stoermer, M. J., Kobe, B. and Young, P. R. (2005). Discovery of antiviral inhibitors targeting the fusion mechanism of the flavivirus family members Dengue, Kunjin and Yellow fever. 30th FEBS Congress - 9th Int Union of Biochem & Molecular Biof, Budapest, 2-7 July, 2005.

Discovery of antiviral inhibitors targeting the fusion mechanism of the flavivirus family members Dengue, Kunjin and Yellow fever

2005

Conference Publication

Development of antiviral drugs targeting the flavivirus fusion mechanism

Kampmann, T., Yennamalli Madhava R, R., Stoermer, M. J., Kobe, B. and Young, P. R. (2005). Development of antiviral drugs targeting the flavivirus fusion mechanism. 30th Lorne Conference on Protein Structure & Function, Lorne, 6-10 Feb, 2005.

Development of antiviral drugs targeting the flavivirus fusion mechanism

2005

Conference Publication

Development of a catalytically active recombinant West Nile NS3 protease and the identification of key enzyme-substrate interactions by site-directed mutagenesis

Chappell, K. J., Stoermer, M. J., Fairlie, D. and Young, P. R. (2005). Development of a catalytically active recombinant West Nile NS3 protease and the identification of key enzyme-substrate interactions by site-directed mutagenesis. International Congress of Virology, San Francisco, 23-27 July, 2005.

Development of a catalytically active recombinant West Nile NS3 protease and the identification of key enzyme-substrate interactions by site-directed mutagenesis

2003

Conference Publication

Template-assembled peptide loops, helices, sheets and nanofibres

Fairlie, DP, Singh, Y, Sharpe, P and Stoermer, M (2003). Template-assembled peptide loops, helices, sheets and nanofibres. 225th National Meeting of the American-Chemical-Society, New Orleans Louisiana, Mar 23-27, 2003. WASHINGTON: AMER CHEMICAL SOC.

Template-assembled peptide loops, helices, sheets and nanofibres

2003

Conference Publication

Macrocyclic peptides as ligands for cellular receptors. When a little rigidity is just right...

Martin J. Stoermer (2003). Macrocyclic peptides as ligands for cellular receptors. When a little rigidity is just right.... Brisbane Biological and Organic Symposium (BBOCS) 2003, Brisbane, 28 November 2003. doi: 10.6084/m9.figshare.7849310

Macrocyclic peptides as ligands for cellular receptors. When a little rigidity is just right...

2003

Conference Publication

Template-assembled peptide loops, helices, sheets, and nanofibers

Fairlie, David P ., Singh, Yogendra, Sharpe, Philip and Stoermer, Martin (2003). Template-assembled peptide loops, helices, sheets, and nanofibers. 225th ACS National Meeting, New Orleans, LA, United States, 23-27 March 2003.

Template-assembled peptide loops, helices, sheets, and nanofibers

2001

Conference Publication

In vitro catalytic activity of recombinant forms of the dengue virus NS3 protease

Young, P. R., Fang, N., Leung, D., Arakaki, T., Stoermer, M. J., Fairlie, D. and Martin, J. L. (2001). In vitro catalytic activity of recombinant forms of the dengue virus NS3 protease. 6th International Symposium on Positive Strand Viruses, Paris, France, 28 May - 2 June, 2001.

In vitro catalytic activity of recombinant forms of the dengue virus NS3 protease

2001

Conference Publication

Are ketoamides suitable electrophilic isosteres for incorporation in inhibitors of serine proteases?

Stoermer, Martin , Leung, Donmienne and Fairlie, David (2001). Are ketoamides suitable electrophilic isosteres for incorporation in inhibitors of serine proteases?. Brisbane Biological & Organic Chemistry Symposium 2001(BBOCS 2001), University of Queensland, Australia, 30 November, 2001.

Are ketoamides suitable electrophilic isosteres for incorporation in inhibitors of serine proteases?

2000

Conference Publication

Towards Arginine Mimetics

Stoermer, Martin and Fairlie, David (2000). Towards Arginine Mimetics. The First Brisbane Biological and Organic Chemistry Symposium, Griifith University, Brisbane, Queensland, Australia, 27th November 2000. doi: 10.6084/m9.figshare.7836131

Towards Arginine Mimetics

2000

Conference Publication

Synthesis, SAR, and Pharmacological Activities of a Series of Tyrosine-Derived Inhibitors of Human Nonpancreatic Secretory Phospholipase A2

Hansford, Karl A. , Clark, Chris I. , Reid, Robert C. , Stoermer, Martin J. , Shiels, Ian , Taylor, Stephen and Fairlie, David P. (2000). Synthesis, SAR, and Pharmacological Activities of a Series of Tyrosine-Derived Inhibitors of Human Nonpancreatic Secretory Phospholipase A2. First Brisbane Biological and Organic Chemistry Symposium, Griffith University, Brisbane, 27 November 2000.

Synthesis, SAR, and Pharmacological Activities of a Series of Tyrosine-Derived Inhibitors of Human Nonpancreatic Secretory Phospholipase A2

2000

Conference Publication

Inhibition of Human Secretory Phospholipase A2 (Type IIA)

Clark, Chris , Reid, Bob , Hansford, Karl , Stoermer, Martin and Fairlie, David (2000). Inhibition of Human Secretory Phospholipase A2 (Type IIA). First Brisbane Biological and Organic Chemistry Symposium, Griffith University, Brisbane, 27 November 2000.

Inhibition of Human Secretory Phospholipase A2 (Type IIA)

1998

Conference Publication

Modelling Studies Of Molecular Receptors

Chalmers, David K., Stoermer, Martin J. and Fairlie, David P. (1998). Modelling Studies Of Molecular Receptors. Royal Australian Chemical Institute 16th National Organic Chemistry Conference, Leura, Blue Mountains, New South Wales, 12-17 July 1998.

Modelling Studies Of Molecular Receptors

1994

Conference Publication

Design and synthesis of inhibitors of HIV-1 protease

Abbenante, Gioavanni , March, Darren , Reid, Robert , Stoermer, Martin , West, Michael , Bergmann, Doug , Alewood, Dianne , Alewood, Paul and Fairlie, David (1994). Design and synthesis of inhibitors of HIV-1 protease. 14th National Conference of the Royal Australian Chemical Institute, Division of Organic Chemistry , University of Wollongong, NSW, Australia, 1994.

Design and synthesis of inhibitors of HIV-1 protease

1993

Conference Publication

Design and synthesis of new cavitands which are stereochemically rigid, hydrophobic and internally functionalised

Stoermer, Martin and Fairle, David (1993). Design and synthesis of new cavitands which are stereochemically rigid, hydrophobic and internally functionalised. Royal Australian Chemical Institute, Division of Medicinal and Agricultural Chemistry and the New Zealand Chemical Institute Conference, Auckland, New Zealand, 1993.

Design and synthesis of new cavitands which are stereochemically rigid, hydrophobic and internally functionalised

1992

Conference Publication

A selective and versatile synthesis of substituted chromones via addition of phenols to dimethyl acetylenedicarboxylate

Stoermer, Martin J. and Fairlie, David P. (1992). A selective and versatile synthesis of substituted chromones via addition of phenols to dimethyl acetylenedicarboxylate. 13th National Conference of the Royal Australian Chemical Institute, Division of Organic Chemistry , Monash University, Melbourne, 1992.

A selective and versatile synthesis of substituted chromones via addition of phenols to dimethyl acetylenedicarboxylate

1992

Conference Publication

Design and synthesis of new cavitands which are stereochemically rigid, hydrophobic and internally functionalised

Stoermer, M.J., Wickramasinghe, W., Weerasuria, K.D.V., Fairlie, D., Butler, D. and Warrener, R. (1992). Design and synthesis of new cavitands which are stereochemically rigid, hydrophobic and internally functionalised. Royal Australian Chemical Institute National Conference 1992, Monash University, Melbourne, Australia, 28 Sept - 2 October 1992.

Design and synthesis of new cavitands which are stereochemically rigid, hydrophobic and internally functionalised