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Synthesis and Antibacterial Activity of New Chiral Aminoalcohol and Benzimidazole Hybrids     
Yazarlar
İlknur Çiçek
 Turgay TUNÇ Turgay TUNÇ
Kırşehir Ahi Evran Üniversitesi, Türkiye
 Hatice ÖĞÜTCÜ Hatice ÖĞÜTCÜ
Kırşehir Ahi Evran Üniversitesi, Türkiye
Suzan Abdurrahmanoğlu
Marmara Üniversitesi, Türkiye
 Aslıhan GÜNEL Aslıhan GÜNEL
Kırşehir Ahi Evran Üniversitesi, Türkiye
 Nadir DEMİREL Nadir DEMİREL
Kırşehir Ahi Evran Üniversitesi, Türkiye
Özet
New chiral aminoalcohol-benzimidazole hybrids have been synthesized from commercially available aminoalcohols. [S(+)-Phenylglycinol, S(−)- Phenylalaninol and S(+)- Leuicinol] and 2-(chloromethyl)-N-tosyl-1-H-benzimidazole. The synthesized compound were characterized by IR, NMR, and LC-MS analysis. The antibacterial properties of aminoalcohol-benzimidazole hybrid molecules 4 a, 4 b, and 4 c were investigated against both gram (+ve) and gram (-ve) bacterial pathogens by the well-diffusion method using several standarts. The cell-based biological experiment was consistent with in silico studies. Furthermore, in silico studies revealed that all synthesized compounds could be suggested as potential drugs for inhibition of both peptide deformylase for bacteria and sterol 14α-demethylase for yeast.
Anahtar Kelimeler
Aminoalcohol | Antibacterial Agent | Benzimidazole | Molecular docking | PDF inhibitor
Makale Türü Özgün Makale
Makale Alt Türü SSCI, AHCI, SCI, SCI-Exp dergilerinde yayımlanan tam makale
Dergi Adı ChemistrySelect
Dergi ISSN 2365-6549
Dergi Tarandığı Indeksler SCI-Expanded
Makale Dili İngilizce
Basım Tarihi 04-2020
Cilt No 5
Sayı 15
Sayfalar 4650 / 4654
Doi Numarası 10.1002/slct.202000355
Makale Linki [{"content-version":"vor","content-type":"application/pdf","intended-application":"text-mining","URL":"https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fslct.202000355"},{"content-version":"vor","content-type":"application/pdf","intended-