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Mark L. Smythe

Researcher at University of Queensland

Publications -  65
Citations -  6427

Mark L. Smythe is an academic researcher from University of Queensland. The author has contributed to research in topics: Cyclic peptide & Linker. The author has an hindex of 26, co-authored 65 publications receiving 6099 citations. Previous affiliations of Mark L. Smythe include Monash University, Parkville campus & Washington University in St. Louis.

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The combinatorial synthesis of bicyclic privileged structures or privileged substructures

TL;DR: Privileged substructures are believed to achieve this through the mimicry of common protein surface elements that are responsible for binding, such as β- and gamma;-turns.
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Rational design of potent sialidase-based inhibitors of influenza virus replication.

TL;DR: Two potent inhibitors based on the crystal structure of influenza virus sialidase have been designed and provide an example of the power of rational, computer-assisted drug design, indicating significant progress in the development of a new therapeutic or prophylactic treatment for influenza infection.
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VALIDATE: A New Method for the Receptor-Based Prediction of Binding Affinities of Novel Ligands

TL;DR: VALIDATE is a hybrid approach to predict the binding affinity of novel ligands for receptors of known three-dimensional structure that calculates physicochemical properties of the ligand and the receptor - ligand complex to estimate the free energy of binding.
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Toward larger chemical libraries: Encoding with fluorescent colloids in combinatorial chemistry

TL;DR: This work introduces an encoding method that involves physically attaching fluorescent colloidal particles to the surface of solid support beads during split and mix syntheses, to produce an information-rich, colored barcode that can be easily, rapidly, and inexpensively decoded using fluorescence microscopy.
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Proteolytic degradation of host hemoglobin by schistosomes.

TL;DR: This paper reviews reports dating from 40 years ago to the present on how schistosomes digest host-derived hemoglobin, and interprets apparent anomalies in some earlier compared to later reports, the latter having benefited from the availability of PCR and gene cloning technologies.