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2004

Journal Article

Increased site 1 affinity improves biopotency of porcine growth hormone - Evidence against diffusion dependent receptor dimerization

Wan, Y., McDevitt, A., Shen, B. J., Smythe, M. L. and Waters, M. J. (2004). Increased site 1 affinity improves biopotency of porcine growth hormone - Evidence against diffusion dependent receptor dimerization. Journal of Biological Chemistry, 279 (43), 44775-44784. doi: 10.1074/jbc.M406092200

Increased site 1 affinity improves biopotency of porcine growth hormone - Evidence against diffusion dependent receptor dimerization

2004

Journal Article

Development of small molecules that mimic the binding of w-conotoxins at the N-type voltage-gated calcium channel

Schroeder, I.C., Smythe, M. L. and Lewis, R. J. (2004). Development of small molecules that mimic the binding of w-conotoxins at the N-type voltage-gated calcium channel. Molecular Diversity, 8 (2), 127-134. doi: 10.1023/B:MODI.0000025656.79632.86

Development of small molecules that mimic the binding of w-conotoxins at the N-type voltage-gated calcium channel

2003

Journal Article

The combinatorial synthesis of bicyclic privileged structures or privileged substructures

Horton, DA, Bourne, GT and Smythe, ML (2003). The combinatorial synthesis of bicyclic privileged structures or privileged substructures. Chemical Reviews, 103 (3), 893-930. doi: 10.1021/cr020033s

The combinatorial synthesis of bicyclic privileged structures or privileged substructures

2003

Journal Article

Difficult macrocyclizations: New strategies for synthesizing highly strained cyclic tetrapeptides

Meutermans, W., Bourne, G. T., Golding, S., Horton, D., Campitelli, M. R., Craik, D. J., Scanlon, M. J. and Smythe, M. L. (2003). Difficult macrocyclizations: New strategies for synthesizing highly strained cyclic tetrapeptides. Organic Letters, 5 (15), 2711-2714. doi: 10.1021/ol034907o

Difficult macrocyclizations: New strategies for synthesizing highly strained cyclic tetrapeptides

2002

Journal Article

Exploring privileged structures: the combinatorial synthesis of cyclic peptides

Horton, D. A., Bourne, G. T. and Smythe, M. L. (2002). Exploring privileged structures: the combinatorial synthesis of cyclic peptides. Journal of Computer-aided Molecular Design, 16 (5-6), 415-431. doi: 10.1023/A:1020863921840

Exploring privileged structures: the combinatorial synthesis of cyclic peptides

2002

Journal Article

A subset-oriented algorithm for minimizing the number of steps required for synthesis of cyclic-peptide libraries

Tran, T. T., Bryant, D. E. and Smythe, M. L. (2002). A subset-oriented algorithm for minimizing the number of steps required for synthesis of cyclic-peptide libraries. Computers and Chemistry, 26 (2), 113-117. doi: 10.1016/S0097-8485(01)00087-0

A subset-oriented algorithm for minimizing the number of steps required for synthesis of cyclic-peptide libraries

2001

Journal Article

The development and application of a novel safety-catch linker for BOC-based assembly of libraries of cyclic peptides

Bourne, Gregory T., Golding, Simon W., McGeary, Ross P., Meutermans, Wim D. F., Jones, Alun, Marshall, Garland R., Alewood, Paul F. and Smythe, Mark L. (2001). The development and application of a novel safety-catch linker for BOC-based assembly of libraries of cyclic peptides. Journal of Organic Chemistry, 66 (23), 7706-7713. doi: 10.1021/jo010580y

The development and application of a novel safety-catch linker for BOC-based assembly of libraries of cyclic peptides

2001

Journal Article

Synthesis of a cyclic peptide library based on the somatostatin sequence using the backbone amide linker approach

Bourne, G.T., Golding, S., Meutermans, W. and Smythe, M.L. (2001). Synthesis of a cyclic peptide library based on the somatostatin sequence using the backbone amide linker approach. Letters in Peptide Science, 7 (6), 311-316. doi: 10.1023/A:1013057832044

Synthesis of a cyclic peptide library based on the somatostatin sequence using the backbone amide linker approach

2001

Journal Article

Proteolysis of human hemoglobin by schistosome cathepsin D

Brindley, P. J., Kalinna, B. H., Wong, J. Y. M., Bogitsh, B. J., King, L. T., Smyth, D. J., Verity, C. K., Abbenante, G., Brinkworth, R. I., Fairlie, D. P., Smythe, M. L., Milburn, P. J., Bielefeldt-Ohmann, H., Zheng, Y. and McManus, D. P. (2001). Proteolysis of human hemoglobin by schistosome cathepsin D. Molecular And Biochemical Parasitology, 112 (1), 103-112. doi: 10.1016/S0166-6851(00)00351-0

Proteolysis of human hemoglobin by schistosome cathepsin D

2000

Journal Article

An Activated O N Acyl Transfer Auxiliary: Efficient Amide-Backbone Substitution of Hindered "Difficult" Peptides

Miranda, L. P., Meutermans, W. D. F., Smythe, M. L. and Alewood, P.F. (2000). An Activated O N Acyl Transfer Auxiliary: Efficient Amide-Backbone Substitution of Hindered "Difficult" Peptides. Journal of Organic Chemistry, 65 (18), 5460-5468. doi: 10.1021/jo991340+

An Activated O N Acyl Transfer Auxiliary: Efficient Amide-Backbone Substitution of Hindered "Difficult" Peptides

2000

Journal Article

Toward larger chemical libraries: Encoding with fluorescent colloids in combinatorial chemistry

Battersby, Bronwyn J., Bryant, Darryn, Meutermans, Wim, Matthews, Daniel, Smythe, Mark L. and Trau, Matt (2000). Toward larger chemical libraries: Encoding with fluorescent colloids in combinatorial chemistry. Journal of the American Chemical Society, 122 (9), 2138-2139. doi: 10.1021/ja993634i

Toward larger chemical libraries: Encoding with fluorescent colloids in combinatorial chemistry

2000

Journal Article

Synthesis of difficult cyclic peptides by inclusion of a novel photolabile auxiliary in a ring contraction strategy

Scolastico, C., Manzoni, L., Meutermans, W. D.F., Golding, S. W., Bourne, G. T., Miranda, L. P., Dooley, M. J., Alewood, P. F. and Smythe, M. L. (2000). Synthesis of difficult cyclic peptides by inclusion of a novel photolabile auxiliary in a ring contraction strategy. Chemtracts, 13 (7), 443-446.

Synthesis of difficult cyclic peptides by inclusion of a novel photolabile auxiliary in a ring contraction strategy

2000

Journal Article

Exploring privileged structures: The combinatorial synthesis of cyclic peptides

Horton, DA, Bourne, GT and Smythe, ML (2000). Exploring privileged structures: The combinatorial synthesis of cyclic peptides. Molecular Diversity, 5 (4), 289-304. doi: 10.1023/A:1021365402751

Exploring privileged structures: The combinatorial synthesis of cyclic peptides

1999

Journal Article

The development of solid phase protocols for a backbone amide linker and its application to the Boc-based assembly of linear peptides

Bourne, G. T., Meutermans, W. D. F. and Smythe, M. L. (1999). The development of solid phase protocols for a backbone amide linker and its application to the Boc-based assembly of linear peptides. Tetrahedron Letters, 40 (40), 7271-7274. doi: 10.1016/S0040-4039(99)01473-2

The development of solid phase protocols for a backbone amide linker and its application to the Boc-based assembly of linear peptides

1999

Journal Article

A Backbone Linker for BOC-Based Peptide Synthesis and On-Resin Cyclization: Synthesis of Stylostatin 1

Bourne, GT, Meutermans, WDF, Alewood, PF, McGeary, RP, Watson, AA and Smythe, ML (1999). A Backbone Linker for BOC-Based Peptide Synthesis and On-Resin Cyclization: Synthesis of Stylostatin 1. Journal of Organic Chemistry, 64 (9), 3095-3101. doi: 10.1021/jo9818780

A Backbone Linker for BOC-Based Peptide Synthesis and On-Resin Cyclization: Synthesis of Stylostatin 1

1997

Journal Article

Proteolytic degradation of host hemoglobin by schistosomes

Brindley, Paul J., Kalinna, Bernd H., Dalton, John P., Day, Sharon R., Wong, Joanna Y. M., Smythe, Mark L. and McManus, Donald P. (1997). Proteolytic degradation of host hemoglobin by schistosomes. Molecular and Biochemical Parasitology, 89 (1), 1-9. doi: 10.1016/S0166-6851(97)00098-4

Proteolytic degradation of host hemoglobin by schistosomes

1997

Journal Article

Synthesis of α-aspartyl-containing cyclic peptides

Meutermans W.D.F., Alewood P.F., Bourne G.T., Hawkins B. and Smythe M.L. (1997). Synthesis of α-aspartyl-containing cyclic peptides. Letters in Peptide Science, 4 (2), 79-84. doi: 10.1007/BF02443518

Synthesis of α-aspartyl-containing cyclic peptides

1997

Journal Article

Synthesis of alpha-aspartyl-containing cyclic peptides

Meutermans, WDF, Alewood, PF, Bourne, GT, Hawkins, B and Smythe, ML (1997). Synthesis of alpha-aspartyl-containing cyclic peptides. Letters In Peptide Science, 4 (2), 79-84. doi: 10.1023/A:1008878017315

Synthesis of alpha-aspartyl-containing cyclic peptides

1996

Journal Article

VALIDATE: A new method for the receptor-based prediction of binding affinities of novel ligands

Head, RD, Smythe, ML, Oprea, TI, Waller, CL, Green, SM and Marshall, GR (1996). VALIDATE: A new method for the receptor-based prediction of binding affinities of novel ligands. Journal of the American Chemical Society, 118 (16), 3959-3969. doi: 10.1021/ja9539002

VALIDATE: A new method for the receptor-based prediction of binding affinities of novel ligands

1996

Journal Article

Electrochemical cyclization of dipeptides to form novel bicyclic, reverse-turn peptidomimetics. 2. Synthesis and conformational analysis of 6,5-bicyclic systems

Slomezynska, Urszula, Chalmers, David K., Cornille, Fabrice, Smythe, Mark L., Beusen, Denise D., Moeller, Kevin D. and Marshall, Garland R. (1996). Electrochemical cyclization of dipeptides to form novel bicyclic, reverse-turn peptidomimetics. 2. Synthesis and conformational analysis of 6,5-bicyclic systems. Journal of Organic Chemistry, 61 (4), 1198-1204. doi: 10.1021/jo950898o

Electrochemical cyclization of dipeptides to form novel bicyclic, reverse-turn peptidomimetics. 2. Synthesis and conformational analysis of 6,5-bicyclic systems