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Showing 1 to 4 of 4 for “"fragment linking"”.

  1. A fragment-based approach towards understanding molecular recognition of 4’-phosphopantetheine adenylyltransferase from Mycobacterium abscessus

    … in this thesis details the application of a fragment-based approach targeting 4’-phosphopantetheine adenylyltransferase (PPAT) from Mycobacterium abscessus (Mabs). A fragment screen of the Abell laboratory 960-member library was conducted by Dr Sherine Thomas (Department of Biochemistry, …

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  2. A Fragment-Based Drug Discovery Approach for the Development of Selective Inhibitors of Protein Kinase CK2

    Over the last twenty years, fragment-based drug discovery (FBDD) has emerged as a highly successful way to provide lead compounds for subsequent optimisation into drug candidates. Initial hits usually exhibit lower potency than those identified by more traditional techniques, such as …

    cambridge Repository record for A Fragment-Based Drug Discovery Approach for the Development of Selective Inhibitors of Protein Kinase CK2 (opens in a new tab)

  3. Biophysical and structural studies of novel F420-dependent oxidoreductases in Mycobacterium tuberculosis

    … and Rv2991 respectively, a novel application of fragment-based approaches was employed. A library of fragments was designed based on known ligands to flavoenzymes and screened for binding to Rv1155 and Rv2991 in the presence and absence of F420 using STD NMR and differential scanning fluorimetry. …

    cambridge Repository record for Biophysical and structural studies of novel F420-dependent oxidoreductases in Mycobacterium tuberculosis (opens in a new tab)

  4. Studies within Fragment-Based Drug Discovery: Library Synthesis and Hit-to-Lead Optimisation

    … projects aimed at addressing challenges within fragment-based drug discovery. The first project describes efforts towards utilising synthetic methodology to address deficiencies within fragment screening collections. This involved the development of a modular, robust and scalable route to access …

    cambridge Repository record for Studies within Fragment-Based Drug Discovery: Library Synthesis and Hit-to-Lead Optimisation (opens in a new tab)