Oxolane Ammonium Salts (Muscarine-Like)—Synthesis and Microbiological Activity - Publikacja - MOST Wiedzy

Wyszukiwarka

Oxolane Ammonium Salts (Muscarine-Like)—Synthesis and Microbiological Activity

Abstrakt

Commercially available 2-deoxy-D-ribose was used to synthesize the appropriate oxolane derivative—(2R,3S)-2-(hydroxymethyl)oxolan-3-ol—by reduction and dehydration/cyclization in an acidic aqueous solution. Its monotosyl derivative, as a result of the quaternization reaction, allowed us to obtain eight new muscarine-type derivatives containing a quaternary nitrogen atom and a hydroxyl group linked to the oxolane ring. Their structure was fully confirmed by the results of NMR, MS and IR analyses. The crystal structure of the pyridinium derivative showed a high similarity of the conformation of the oxolane ring to previously published crystal structures of muscarine. Two reference strains of Gram-negative bacteria (Escherichia coli ATCC 25922 and Pseudomonas aeruginosa ATCC 27853), two reference strains of Gram-positive staphylococci (Staphylococcus aureus ATCC 25923 and Staphylococcus aureus ATCC 29213) and four reference strains of pathogenic yeasts of the genus Candida spp. (Candida albicans SC5314, Candida glabrata DSM 11226, Candida krusei DSM 6128 and Candida parapsilosis DSM 5784) were selected for the evaluation of the antimicrobial potential of the synthesized compounds. The derivative containing the longest (decyl) chain attached to the quaternary nitrogen atom turned out to be the most active.

Cytowania

  • 0

    CrossRef

  • 0

    Web of Science

  • 0

    Scopus

Autorzy (6)

Słowa kluczowe

Informacje szczegółowe

Kategoria:
Publikacja w czasopiśmie
Typ:
artykuły w czasopismach
Opublikowano w:
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES nr 25,
ISSN: 1661-6596
Język:
angielski
Rok wydania:
2024
Opis bibliograficzny:
Bogdanowicz P., Madaj J., Szweda P., Sikorski A., Samaszko-Fiertek J., Dmochowska B.: Oxolane Ammonium Salts (Muscarine-Like)—Synthesis and Microbiological Activity// INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES -,iss. 4 (2024), s.2368-
DOI:
Cyfrowy identyfikator dokumentu elektronicznego (otwiera się w nowej karcie) 10.3390/ijms25042368
Źródła finansowania:
  • Praca sfinansowana przez pracowników UG.
  • Publikacja bezkosztowa
Weryfikacja:
Politechnika Gdańska

wyświetlono 53 razy

Publikacje, które mogą cię zainteresować

Meta Tagi