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Wyświetlanie 1-3 z 3
Tytuł:
The Synthesis and Evaluation of Diethyl Benzylphosphonates as Potential Antimicrobial Agents
Autorzy:
Szymczak, Mateusz
Favi, Gianfranco
Brodzka, Anna
Trzepizur, Damian
Ostaszewski, Ryszard
Kowalczyk, Paweł
Kramkowski, Karol
Koszelewski, Dominik
Wypych, Aleksandra
Lizut, Rafał
Współwytwórcy:
Favi, Gianfranco
Wydawca:
MDPI
Cytata wydawnicza:
Molecules 2022, 27(20), 6865; https://doi.org/10.3390/molecules27206865
Opis:
The impact of substituent at phenyl ring of diethyl benzylphosphonate derivatives on cytotoxic activity was studied. The organophosphonates were obtained based on developed palladium-catalyzed α, β-homodiarylation of vinyl esters protocol. The new synthetic pathway toward 1,2-bis(4-((diethoxyphosphoryl)methyl)phenyl)ethyl acetate was proposed which significantly improves the overall yield of the final product (from 1% to 38%). Several newly synthesized organophosphonates were tested as new potential antimicrobial drugs on model Escherichia coli bacterial strains (K12 and R2-R3). All tested compounds show the highest selectivity and activity against K12 and R2 strains. Preliminary cellular studies using MIC and MBC tests and digestion of Fpg after modification of bacterial DNA suggest that selected benzylphosphonate derivatives may have greater potential as antibacterial agents than typically used antibiotics such as ciprofloxacin, bleomycin and cloxacillin. These compounds are highly specific for pathogenic E. coli strains based on the model strains used and may be engaged in the future as new substitutes for commonly used antibiotics, which is especially important due to the increasing resistance of bacteria to various drugs and antibiotics.
National Science Center, OPUS No. 2019/33/B/ST4/01118; grant from the Medical University of Białystok SUB/2/DN/22/001/2201
Dostawca treści:
Repozytorium Centrum Otwartej Nauki
Artykuł
Tytuł:
Promiscuous Lipase-Catalyzed Markovnikov Addition of H-Phosphites to Vinyl Esters for the Synthesis of Cytotoxic α-Acyloxy Phosphonate Derivatives
Autorzy:
Ostaszewski, Ryszard
Gawdzik, Barbara
Perez Antoñanzas, Roman
Samsonowicz-Górski, Jan
Kramkowski, Karol
Kowalczyk, Paweł
Koszelewski, Dominik
Wypych, Aleksandra
Lizut, Rafał
Współwytwórcy:
Perez Antoñanzas, Roman
Wydawca:
MDPI
Cytata wydawnicza:
Kowalczyk, P.; Koszelewski, D.; Gawdzik, B.; Samsonowicz-Górski, J.; Kramkowski, K.; Wypych, A.; Lizut, R.; Ostaszewski, R. Promiscuous Lipase-Catalyzed Markovnikov Addition of H-Phosphites to Vinyl Esters for the Synthesis of Cytotoxic α-Acyloxy Phosphonate Derivatives. Materials 2022, 15, 1975. https://doi.org/10.3390/ma15051975
Opis:
An enzymatic route for phosphorous-carbon- bond formation is developed by discovering new promiscuous activity of lipase. This biocatalytic transformation of phosphorous-carbon- bond addition leads to biologically and pharmacologically relevant α-acyloxy phosphonates with methyl group in α-position. A series of target compounds were synthesized with yields ranging from 54% to 83% by enzymatic reaction with Candida cylindracea (CcL) lipase via Markovnikov addition of H-phosphites to vinyl esters. We carefully analyzed the best conditions for the given reaction such as the type of enzyme, temperature, and type of solvent. The developed protocol is applicable to a range of H-phosphites and vinyl esters significantly simplifying the preparation of synthetically challenging α-pivaloyloxy phosphonates. Further, the obtained compounds were validated as new potential antimicrobial drugs with characteristic E. coli bacterial strains and DNA modification recognized by the Fpg protein, N-methyl purine glycosylases as new substrates. The impact of the methyl group located in the α-position of the studied α-acyloxy phosphonates on the antimicrobial activity was demonstrated. The pivotal role of this group on inhibitory activity against selected pathogenic E. coli strains was revealed. The observed results are especially important in the case of the increasing resistance of bacteria to various drugs and antibiotics.
Medical University of Białystok (SUB/2/DN/22/001/2201) National Science Center, Poland, (project OPUS No. 2019/33/B/ST4/01118)
Dostawca treści:
Repozytorium Centrum Otwartej Nauki
Artykuł
Tytuł:
The Evaluation of DHPMs as Biotoxic Agents on Pathogen Bacterial Membranes
Autorzy:
Brodzka, Anna
Ostaszewski, Ryszard
Gawdzik, Barbara
Neacsu, Ionela Andreea
Kowalczyk, Paweł
Kramkowski, Karol
Koszelewski, Dominik
Wypych, Aleksandra
Masternak, Joanna
Współwytwórcy:
Neacsu, Ionela Andreea
Wydawca:
MDPI
Cytata wydawnicza:
Gawdzik, B.; Kowalczyk, P.; Koszelewski, D.; Brodzka, A.; Masternak, J.; Kramkowski, K.; Wypych, A.; Ostaszewski, R. The Evaluation of DHPMs as Biotoxic Agents on Pathogen Bacterial Membranes. Membranes 2022, 12, 238. https://doi.org/10.3390/ membranes12020238
Opis:
Herein, we present biological studies on 3,4-dihydropyrimidin-2(1H)-ones (DHPMs) obtained via Biginelli reaction catalyzed by NH4Cl under solvent-free conditions. Until now, DHPMs have not been tested for biological activity against pathogenic E. coli strains. We tested 16 newly synthesized DHPMs as antimicrobial agents on model E. coli strains (K12 and R2–R4). Preliminary cellular studies using MIC and MBC tests and digestion of Fpg after modification of bacterial DNA suggest that these compounds may have greater potential as antibacterial agents than typically used antibiotics, such as ciprofloxacin (ci), bleomycin (b) and cloxacillin (cl). The described compounds are highly specific for pathogenic E. coli strains based on the model strains used and may be engaged in the future as new substitutes for commonly used antibiotics in clinical and nosocomial infections in the pandemic era.
Medical University of Białystok (grant SUB/2/DN/22/001/2201) National Science Center (OPUS No. 2019/33/B/ST4/01118)
Dostawca treści:
Repozytorium Centrum Otwartej Nauki
Artykuł
    Wyświetlanie 1-3 z 3

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