Dr Martin Stoermer
Dr

Martin Stoermer

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Background

I am a medicinal and organic chemist

Studied organic chemistry at the University of Sydney, moved to UQ in 1993, then worked for Bayer in Germany, before moving back to Australia in 1996. Worked in Melbourne at the Victorian College of Pharmacy (now MIPS). I then returned to UQ in 2000 to the Fairlie lab where we design and synthesise new chemical entities to tackle human disease. Since 2012 I have been on extended medical leave and am currently an Adjunct Research Fellow, researching proteins from flaviviruses such as Dengue, West Nile, and Zika viruses, and the coronaviruses SARS, MERS, and SARS-CoV-2.

Availability

Dr Martin Stoermer is:
Available for supervision

Fields of research

Biological Sciences Medicinal and biomolecular chemistry Pharmacology and pharmaceutical sciences

Qualifications

  • Bachelor (Honours) of Science (Advanced), University of Sydney
  • Doctor of Philosophy, University of Sydney

Research interests

  • Viral Proteases

    I study the proteases from Flaviviruses such as Dengue and West Nile virus, and Coronaviruses like SARS, and SARS-CoV-2, using a combination of chemical synthesis and molecular modelling. Previously I worked on the design and synthesis of inhibitors of HIV protease.

Search Professor Martin Stoermer’s works on UQ eSpace

119 works between 1986 and 2020
All (119) Journal Article (67) Conference Publication (44) Other Outputs (8)

101 - 119 of 119 works

1998

Journal Article

(E)-3-Methyl-5-phenyl-2-pentenoic Acid

Stoermer, Martin and Pinhey, John (1998). (E)-3-Methyl-5-phenyl-2-pentenoic Acid. Molecules, 3 (8), M53. doi: 10.3390/m53

(E)-3-Methyl-5-phenyl-2-pentenoic Acid

1998

Journal Article

[(Z)-5-Phenyl-2-penten-2-yl]mercury Acetate

Stoermer, Martin and Pinhey, John (1998). [(Z)-5-Phenyl-2-penten-2-yl]mercury Acetate. Molecules, 3 (8), M69. doi: 10.3390/m69

[(Z)-5-Phenyl-2-penten-2-yl]mercury Acetate

1998

Journal Article

Tributyl-[(Z)-5-phenyl-2-penten-2-yl]stannane

Stoermer, Martin and Pinhey, John (1998). Tributyl-[(Z)-5-phenyl-2-penten-2-yl]stannane. Molecules, 3 (3), M67. doi: 10.3390/m67

Tributyl-[(Z)-5-phenyl-2-penten-2-yl]stannane

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

1996

Journal Article

Structure-activity relationships for macrocyclic peptidomimetic inhibitors of HIV-1 protease.

Abbenante, G., Bergman, D. A., Brinkworth, R. I., March, D. R., Reid, R. C., Hunt, P. A., James, I. W., Dancer, R. J., Garnham, B., Stoermer, M. L. and Fairlie, D. P. (1996). Structure-activity relationships for macrocyclic peptidomimetic inhibitors of HIV-1 protease.. Bioorganic & Medicinal Chemistry Letters, 6 (21), 2531-2536. doi: 10.1016/0960-894X(96)00468-4

Structure-activity relationships for macrocyclic peptidomimetic inhibitors of HIV-1 protease.

1996

Journal Article

1H NMR evidence for the formation of vinyllead triacetates. The reactions of vinylmercury, vinyltin, and vinylboronic acids with lead tetraacetate

Parkinson, Christopher J. and Stoermer, Martin J. (1996). 1H NMR evidence for the formation of vinyllead triacetates. The reactions of vinylmercury, vinyltin, and vinylboronic acids with lead tetraacetate. Journal of Organometallic Chemistry, 507 (1-2), 207-214. doi: 10.1016/0022-328x(95)05746-c

1H NMR evidence for the formation of vinyllead triacetates. The reactions of vinylmercury, vinyltin, and vinylboronic acids with lead tetraacetate

1995

Journal Article

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

Stoermer, Martin J. and Fairlie, David P. (1995). A selective and versatile synthesis of substituted chromones via addition of phenols to dimethyl acetylenedicarboxylate. Australian Journal of Chemistry, 48 (3), 677-686. doi: 10.1071/CH9950677

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

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

Journal Article

Flavones are inhibitors of HIV-1 proteinase

Brinkworth R.I., Stoermer M.J. and Fairlie D.P. (1992). Flavones are inhibitors of HIV-1 proteinase. Biochemical and Biophysical Research Communications, 188 (2), 631-637. doi: 10.1016/0006-291X(92)91103-W

Flavones are inhibitors of HIV-1 proteinase

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

1992

Journal Article

Electrophilic vinylations by vinyllead triacetates and tribenzoates generated by tin–lead exchange

Parkinson, Christopher J., Pinhey, John T. and Stoermer, Martin J. (1992). Electrophilic vinylations by vinyllead triacetates and tribenzoates generated by tin–lead exchange. Journal of the Chemical Society, Perkin Transactions 1 (15), 1911-1915. doi: 10.1039/p19920001911

Electrophilic vinylations by vinyllead triacetates and tribenzoates generated by tin–lead exchange

1991

Journal Article

Vinyl cation formation by decomposition of vinyllead(IV) triacetates. Part 2

Pinhey, John T. and Stoermer, Martin J. (1991). Vinyl cation formation by decomposition of vinyllead(IV) triacetates. Part 2. Journal of the Chemical Society, Perkin Transactions 1 (10), 2455-2460. doi: 10.1039/p19910002455

Vinyl cation formation by decomposition of vinyllead(IV) triacetates. Part 2

1991

Conference Publication

Synthesis of cavitands as catalytic environments

Stoermer, Martin J. and Fairlie, David P. (1991). Synthesis of cavitands as catalytic environments. 12th National Conference of the Royal Australian Chemical Institute, Division of Organic Chemistry, University of Queensland, Australia, 1991.

Synthesis of cavitands as catalytic environments

1990

Conference Publication

The alpha-vinylation of beta-dicarbonyl compounds via vinyllead triacetates

Stoermer, Martin J. (1990). The alpha-vinylation of beta-dicarbonyl compounds via vinyllead triacetates. Royal Australian Chemical Institute, Fifth Brisbane Organic Chemistry Symposium (BOCS), Griffith University, Brisbane, Australia, 1990.

The alpha-vinylation of beta-dicarbonyl compounds via vinyllead triacetates

1990

Journal Article

Vinyl cation formation by decomposition of vinyl-lead triacetates. The reactions of vinylmercury and vinyltin compounds with lead tetra-acetate

Moloney, Mark G., Pinhey, John T. and Stoermer, Martin J. (1990). Vinyl cation formation by decomposition of vinyl-lead triacetates. The reactions of vinylmercury and vinyltin compounds with lead tetra-acetate. Journal of the Chemical Society, Perkin Transactions 1 (10), 2645-2655. doi: 10.1039/p19900002645

Vinyl cation formation by decomposition of vinyl-lead triacetates. The reactions of vinylmercury and vinyltin compounds with lead tetra-acetate

1989

Conference Publication

Vinyllead triacetates: a source of vinyl cations or alkylidene carbenes?

Stoermer, Martin J. and Pinhey, John T. (1989). Vinyllead triacetates: a source of vinyl cations or alkylidene carbenes?. 11th National Conference of the Royal Australian Chemical Institute, Division of Organic Chemistry , James Cook University of North Queensland, Townsville, 1989.

Vinyllead triacetates: a source of vinyl cations or alkylidene carbenes?

1986

Conference Publication

Generation of vinyl cations from vinyllead triacetates

Stoermer, Martin J. , Moloney, Mark L. and Pinhey, John T. (1986). Generation of vinyl cations from vinyllead triacetates. 9th National Conference of the Royal Australian Chemical Institute, Division of Organic Chemistry , University of Adelaide and Flinders University, South Australia, 1986.

Generation of vinyl cations from vinyllead triacetates

Past funding

  • 2014
    Continuous-Flow Hydrogenation Reactor (H-Cube Pro)
    UQ Major Equipment and Infrastructure
    Open grant

Availability

Dr Martin Stoermer is:
Available for supervision

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Supervision history

Completed supervision

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