Molecules · 2022 · 15 citations · 27 references
Natural SciencesChemistryMedicinal ChemistryInorganic ChemistryOrganic ChemistryOrganometallic ChemistryCoordination ChemistryCrystal ChemistryHeterocyclic ChemistryOrganometallic SynthesisAntimony ChemistryChemical Structure-activity RelationshipsOrganometallic AntimicrobialsOrganometallic ComplexesTrigonal Bipyramidal Coordination
A series of the eight novel organoantimony(V) cyanoximates of Sb(C6H5)4L composition was synthesized using the high-yield heterogeneous metathesis reaction between solid AgL (or TlL) and Sb(C6H5)4Br in CH3CN at room temperature. Cyanoximes L were specially selected from a large group of 48 known compounds of this subclass of oximes on the basis of their water solubility and history of prior biological activity. The synthesized compounds are well soluble in organic solvents and were studied using a variety of conventional spectroscopic and physical methods. The crystal structures of all reported organometallic compounds were determined and revealed the formation of the distorted trigonal bipyramidal environment of the Sb atom and monodentate axial binding of acido-ligands via the O atom of the oxime group. The compounds are thermally stable in the solid state and in solution molecular compounds. For the first time, this specially designed series of organoantimony(V) compounds is investigated as potential non-antibiotic antimicrobial agents against three bacterial and two fungal human pathogens known for their increasing antimicrobial resistance. Bacterial pathogens included Gram-negative Escherichia coli and Pseudomonas aeruginosa, and Gram-positive Staphylococcus aureus. Fungal pathogens included Cryptococcus neoformans and Candida albicans. The cyanoximates alone showed no antimicrobial impact, and the incorporation of the SbPh4 group enabled the antimicrobial effect. Overall, the new antimony compounds showed a strong potential as both broad- and narrow-spectrum antimicrobials against selected bacterial and fundal pathogens and provide insights for further synthetic modifications of the compounds to increase their activities.
27
Complete genome sequence of Pseudomonas aeruginosa PAO1, an opportunistic pathogen
C. Kendall Stover, X. Q. Pham, Alice L. Erwin et al. · Nature · 2000 · 4.6K citations · Full text
Whole genome sequencing of meticillin-resistant Staphylococcus aureus
Makoto Kuroda, Toshiko Ohta, Ikuo Uchiyama et al. · The Lancet · 2001 · 2K citations · Full text
Concentration-dependent activity in natural environments
Steve P. Bernier, Michael G. Surette · Frontiers in Microbiology · 2013 · 262 citations · Full text
Life Sciences, Ecology, Microbiology +17