Journals / Selçuk Üniversitesi Fen Fakültesi Fen Dergisi / 2023 / Cilt: 49 Sayı: 2

Synthesis, characterization and investigation of antimicrobial activities of salts of 2-aminopyridine derivatives and 2-methoxy-5-sulfamoylbenzoic acid

2-Aminopiridin türevleri ile 2-metoksi-5-sülfamoyilbenzoik asit tuzlarının sentezi, karakterizasyonu, antimikrobiyal aktivitelerinin incelenmesi

Pages
53–63
Publication Date
2023-10-30
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

The best activity values of the compounds were observed 2Bzap and 2a3OHp (31.25 µg/mL) in B. subtilis bacteria, all compounds (except Hsba) (62.50 µg/mL) in E. faecalis and S. aureus bacteria, 2a3OHpsba (15.60 µg/mL) in E. coli bacteria, 2Bzapsba, Hsba, 2Bzap, 2amp and 2a3OHp (31.25 µg/mL) in L. monocytogenes bacteria, Hsba (31.25 µg/mL) in P. aeruginoa bacteria and 2Bzap (31.25 µg/mL) in C. albicans yeast.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:In this study, proton transfer salts (2apsba, 2Bzapsba, 2ampsba and 2a3OHpsba) between 2-methoxy-5-sulfamoylbenzoic acid (Hsba) and 2-aminopyridine (ap), 2-benzylaminopyridine (2Bzap), 2-aminomethylpyridine (2amp) and 2-amino-3-hydroxypyridine (2a3OHp) were synthesized.
📊
Key Findings & Data:Starting materials and proton transfer salts of Enterococcus faecalis (ATCC 29212), Listeria monocytogenes (ATCC 7644), Bacillus subtilis, Staphylococcus aureus (NRRL-B 767) (Gram positive), Escherichia coli (ATCC 25922) and Pseudomonas aeruginosa (ATCC 27853) (Gram negative) bacteria and Candida Albicans (ATCC 14053) yeast of antibacterial and antifungal activities against were investigated.
💡
Conclusion & Impact:The best activity values of the compounds were observed 2Bzap and 2a3OHp (31.25 µg/mL) in B. subtilis bacteria, all compounds (except Hsba) (62.50 µg/mL) in E. faecalis and S. aureus bacteria, 2a3OHpsba (15.60 µg/mL) in E. coli bacteria, 2Bzapsba, Hsba, 2Bzap, 2amp and 2a3OHp (31.25 µg/mL) in L. monocytogenes bacteria, Hsba (31.25 µg/mL) in P. aeruginoa bacteria and 2Bzap (31.25 µg/mL) in C. albicans yeast.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:2-Metoksi-5-sülfamoyilbenzoik asit · 2-Aminopiridin · Proton Transfer Tuzu

Abstract

In this study, proton transfer salts (2apsba, 2Bzapsba, 2ampsba and 2a3OHpsba) between 2-methoxy-5-sulfamoylbenzoic acid (Hsba) and 2-aminopyridine (ap), 2-benzylaminopyridine (2Bzap), 2-aminomethylpyridine (2amp) and 2-amino-3-hydroxypyridine (2a3OHp) were synthesized. Starting materials and proton transfer salts of Enterococcus faecalis (ATCC 29212), Listeria monocytogenes (ATCC 7644), Bacillus subtilis, Staphylococcus aureus (NRRL-B 767) (Gram positive), Escherichia coli (ATCC 25922) and Pseudomonas aeruginosa (ATCC 27853) (Gram negative) bacteria and Candida Albicans (ATCC 14053) yeast of antibacterial and antifungal activities against were investigated. Antifungal activities were compared with Fluconazole and antibacterial activities with Cefepime, Vancomycin and Levofloxacin. The compounds used and synthesized in the experiment have activity against bacteria and yeasts. The best activity values of the compounds were observed 2Bzap and 2a3OHp (31.25 µg/mL) in B. subtilis bacteria, all compounds (except Hsba) (62.50 µg/mL) in E. faecalis and S. aureus bacteria, 2a3OHpsba (15.60 µg/mL) in E. coli bacteria, 2Bzapsba, Hsba, 2Bzap, 2amp and 2a3OHp (31.25 µg/mL) in L. monocytogenes bacteria, Hsba (31.25 µg/mL) in P. aeruginoa bacteria and 2Bzap (31.25 µg/mL) in C. albicans yeast.

Özet

Bu çalışmada, 2-metoksi-5-sülfamoyilbenzoik asit (Hsba) ile 2-aminopiridin (ap), 2-benzilaminopiridin (2Bzap), 2-aminometilpiridin (2amp) ve 2-amino-3-hidroksipiridin (2a3OHp)’in proton transfer tuzları (2apsba, 2Bzapsba, 2ampsba ve 2a3OHpsba) sentezlenmiştir. Başlangıç maddeleri ve proton transfer tuzlarının Enterococcus faecalis (ATCC 29212), Listeria monocytogenes (ATCC 7644), Bacillus subtilis, Staphylococcus aureus (NRRL-B 767) (Gram pozitif), Escherichia coli (ATCC 25922) ve Pseudomonas aeruginosa (ATCC 27853) (Gram negatif) bakterilerine ve Candida Albicans (ATCC 14053) mayasına karşı antibakteriyel ve antifungal aktiviteleri incelenmiştir. Antifungal aktiviteler Flukonazol ile antibakteriyel aktiviteleri ise Sefepim, Vankomisin ve Levofloksasin ile kıyaslanmıştır. Deneyde kullanılan ve sentezlenen bileşikler bakteri ve mayalara karşı aktiviteye sahiptir. Bileşiklerin en iyi aktivite değerleri B. subtilis bakterisinde 2Bzap ve 2a3OHp (31,25 µg/mL), E. faecalis ve S. aureus bakterilerinde tüm bileşikler (Hsba hariç) (62,50 µg/mL), E. coli bakterisinde 2a3OHpsba (15,60 µg/mL), L. monocytogenes bakterisinde Hsba, 2Bzap, 2amp ve 2a3OHp (31,25 µg/mL), P. aeruginoa bakterisinde Hsba (31,25 µg/mL) ve C. albicans mayasında 2Bzap (31,25 µg/mL)’de gözlenmiştir.

🔖

Cite This Article

İLKİMEN, H., YENİKAYA, C., GÜLBANDILAR, A. (2023). Synthesis, characterization and investigation of antimicrobial activities of salts of 2-aminopyridine derivatives and 2-methoxy-5-sulfamoylbenzoic acid. Selçuk Üniversitesi Fen Fakültesi Fen Dergisi, Cilt: 49 Sayı: 2, 53–63. https://ajindex.com/articles/969778

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (13)

  1. Avan, İ., Güven, A., Güven K. 2013, Synthesis and antimicrobial investigation of some 5H-pyridazino[4,5-b]indoles. Turkish Journal of Chemistry, 37: 271-291.
  2. Berge, S. M., Bighley, L. D., Monkhouse, D. C., 1977, Pharmaceutical salts. Journal of Pharmaceutical Sciences, 66, 1-19.
  3. Choan, Z. H., Hassan, M., Khan, M. K., Supuran, C. T., 2005, In-vitro antibacterial, antifungal and cytotoxic properties of sulfonamide-derived Schiff's bases and their metal complexes. Journal of Enzyme Inhibition and Medicinal Chemistry, 20, 183-188.
  4. Fuhrmann, H., Brenner, S., Arndt, P., Kempe, R., 1996, Octahedral group 4 metal complexes that contain amine, amido, and aminopyridinato ligands: synthesis, structure, and application in α-olefin oligo- and polymerization, Inorganic Chemistry, 35, 6742-6745.
  5. Hamor, G. H., Reavlin, B. L., 1967, Anticonvulsants III: Alkyl esters of 4-bromo-2-sulfamoylbenzoic acid and 4-chloro-2-sulfamoylbenzoic acid. Journal of Pharmaceutical Sciences, 56, 134-136.
  6. Haynes, D. A., Jones, W., Motherwell, W. D. S., 2005, Occurrence of pharmaceutically acceptable anions and cations in the Cambridge Structural Database. Journal of Pharmaceutical Sciences, 94, 2111-2120.
  7. İlkimen, H., 2019, Synthesis and characterization of mixed ligand Cu(II) complexes of 2-methoxy-5-sulfamoylbenzoic acid and 2 aminopyridine derivatives. Macedonian Journal of Chemistry and Chemical Engineering, 38(1), 13-17.
  8. İlkimen, H., Salün, S. G., Yenikaya, C. 2-Metoksi-5-sülfamoyilbenzoik asitin metal komplekslerinin sentezi ve karakterizasyonu. SOCRATES 1st International Health, Engineering and Applied Sciences Congress. 19-20 Haziran 2021b,
  9. Ankara,
  10. Türkiye. İlkimen, H., Salün, S. G., Yenikaya, C., 2020, Sülfamoyilbenzoik asit türevlerinin Fe(III) metal komplekslerinin sentezi ve karakterizasyonu. Euroasia Journal Of Mathematics-Engineering Natural, Medical Sciences, 8, 108-116.
  11. İlkimen, H., Türken, N., Gülbandılar, A., 2021a, Synthesis, characterization, antimicrobial and antifungal activity of studies of two novel aminopyridine-sulfamoylbenzoic acid salts and their Cu(II) complexes. Journal of the Iranian Chemical Society, 18, 1941-1946.
  12. İlkimen, H., Yenikaya, C., Gülbandılar, A., 2-Metoksi-5-sulfamoyilbenzoik asit ile 2,3-diaminopiridin türevlerinin proton transfer tuzları ve Cu(II) komplekslerinin sentezi, karakterizasyonu, antimikrobiyal özelliklerinin incelenmesi. III. Baskent International Conference On Multidisciplinary Studies, September 23-25, 2022,
  13. Ankara, Türkiye. Kaplancık