The following articles (labelled with PubMed ID or TBD) are for your review
PMID | Data | Article Title | Organization |
12467623 |
38 |
Design and synthesis of novel benzofurans as a new class of antifungal agents targeting fungal N-myristoyltransferase. Part 3. |
Nippon Roche Research Center |
11844682 |
36 |
Design and synthesis of novel benzofurans as a new class of antifungal agents targeting fungal N-myristoyltransferase. Part 2. |
Nippon Roche Research Center |
11459642 |
39 |
Design and synthesis of novel benzofurans as a new class of antifungal agents targeting fungal N-myristoyltransferase. Part 1. |
Nippon Roche Research Center |
26962429 |
15 |
Discovery of high affinity inhibitors of Leishmania donovani N-myristoyltransferase. |
Imperial College |
26962430 |
20 |
Discovery of pyridyl-based inhibitors of Plasmodium falciparum N-myristoyltransferase. |
Imperial College |
25412409 |
51 |
Lead optimization of a pyrazole sulfonamide series of Trypanosoma brucei N-myristoyltransferase inhibitors: identification and evaluation of CNS penetrant compounds as potential treatments for stage 2 human African trypanosomiasis. |
University of Dundee |
25238611 |
9 |
Structure-based design of potent and selective Leishmania N-myristoyltransferase inhibitors. |
Imperial College |
23170970 |
7 |
Discovery of novel and ligand-efficient inhibitors of Plasmodium falciparum and Plasmodium vivax N-myristoyltransferase. |
Imperial College |
23035716 |
32 |
Design and synthesis of inhibitors of Plasmodium falciparum N-myristoyltransferase, a promising target for antimalarial drug discovery. |
Imperial College |
22439843 |
32 |
Discovery of Plasmodium vivax N-myristoyltransferase inhibitors: screening, synthesis, and structural characterization of their binding mode. |
Imperial College |
22148754 |
26 |
Discovery of a novel class of orally active trypanocidal N-myristoyltransferase inhibitors. |
University of Dundee |
20149656 |
14 |
Derivatives of aryl amines containing the cytotoxic 1,4-dioxo-2-butenyl pharmacophore. |
Acadia University |
| 11 |
A chiral recognition element with an unusual size constraint affects the potency and selectivity for peptidomimetic inhibitors of Candida albicans myristoyl-CoA:protein N-myristoyltransferase |
TBA |
32575985 |
38 |
Novel Thienopyrimidine Inhibitors of |
Imperial College London |
31913033 |
12 |
Fragment-to-Lead Medicinal Chemistry Publications in 2018. |
Frontier Medicines |
31423787 |
77 |
How To Design Selective Ligands for Highly Conserved Binding Sites: A Case Study Using |
Johannes Gutenberg-Universit£T Mainz |
9258368 |
38 |
Design and synthesis of novel imidazole-substituted dipeptide amides as potent and selective inhibitors of Candida albicans myristoylCoA:protein N-myristoyltransferase and identification of related tripeptide inhibitors with mechanism-based antifungal activity. |
G.D. Searle |
7783114 |
21 |
Design and syntheses of potent and selective dipeptide inhibitors of Candida albicans myristoyl-CoA:protein N-myristoyltransferase. |
G.D. Searle And |
30207721 |
58 |
A Molecular Hybridization Approach for the Design of Potent, Highly Selective, and Brain-Penetrant N-Myristoyltransferase Inhibitors. |
University of Dundee |
29125744 |
38 |
Design and Synthesis of Brain Penetrant Trypanocidal N-Myristoyltransferase Inhibitors. |
University of Dundee |