ACS Infectious Diseases · 2019 · 28 citations · 17 references
PharmacyMedicinal ChemistryMicrobiologyDrug DesignDrug DiscoveryStructural BiologyChemical Space ExplorationPermeability AssessmentResistance In Gram-negative BacteriaDesign CriteriaMinimum Inhibitory Concentration DeterminationOuter Membrane PermeabilityOuter Membrane PorinsPore Formation MechanismsPorin FunctionPorin ProteinsReduced Membrane Permeability
Monobactam antibiotic 1 is active against Gram-negative bacteria even though it has a higher molecular weight (MW) than the limit of 600 Da typically applied in designing such compounds. On the basis of 2D NMR data, the compound is able to adopt a compact conformation. The dimensions, projection area, and dipole moment derived from this conformation are compatible with porin permeation, as are locations of polar groups upon superimposition to the crystal structure of ampicillin bound to E. coli OmpF porin. Minimum inhibitory concentration (MIC) shifts in a porin knock-out strain are also consistent with 1 predominately permeating through porins. In conclusion, we describe a carefully characterized case of a molecule outside default design parameters where MW does not adequately represent the 3D shape more directly related to permeability. Leveraging 3D design criteria would open up additional chemical space currently underutilized due to limitations perceived in 2D.
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van der Waals Volumes and Radii
A. Bondì · The Journal of Physical Chemistry · 1964 · 19.2K citations
Akinobu Ito, Toru Nishikawa, Shuhei Matsumoto et al. · Antimicrobial Agents and Chemotherapy · 2016 · 333 citations · Full text