| Makale Türü | Özgün Makale (SSCI, AHCI, SCI, SCI-Exp dergilerinde yayınlanan tam makale) | ||
| Dergi Adı | Journal of the Iranian Chemical Society (Q3) | ||
| Dergi ISSN | 1735-207X Wos Dergi Scopus Dergi | ||
| Dergi Tarandığı Indeksler | SCI-Expanded | ||
| Makale Dili | İngilizce | Basım Tarihi | 02-2022 |
| Cilt / Sayı / Sayfa | 19 / 2 / 563–577 | DOI | 10.1007/s13738-021-02331-8 |
| Makale Linki | http://dx.doi.org/10.1007/s13738-021-02331-8 | ||
| UAK Araştırma Alanları |
Organik Kimya
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| Özet |
| In this study, it was aimed to synthesize novel molecules containing potential biological active phenolic Mannich base moiety and evaluate the inhibition properties against α-glycosidase (α-Gly) and acetylcholinesterase (AChE). For this purpose, phenolic aldehydes (1–3) were synthesized from 4-hydroxy-3-methoxy benzaldehyde (vanillin) according to the Mannich Reaction. Five different carboxylic acid hydrazides (4a-e) were synthesized from esters obtained from carboxylic acids. Fifteen Schiff base derivatives (5a-e, 6a-e, and 7a-e) were synthesized from the condensation reaction of compounds 1–3 with 4a-e. In this work, a series of novel Schiff bases from Phenolic Mannich bases (5a-e, 6a-e, and 7a-e) were tested toward α-Gly and AChE enzymes. Compounds 5a-e, 6a-e, and 7a-e showed Kis in ranging of 341.36 ± 31.84–904.76 ± 93.56 nM on AChE and 176.27 ± 22.87—621.77 ± 69.98 nM on α … |
| Anahtar Kelimeler |
| Enzyme inhibition | Molecular docking | Phenolic Mannich bases | Schiff bases |
| Atıf Sayıları | |
| Web of Science | 45 |
| Scopus | 44 |
| Google Scholar | 56 |
| Dergi Adı | Journal of the Iranian Chemical Society |
| Yayıncı | Springer Verlag |
| Açık Erişim | Hayır |
| ISSN | 1735-207X |
| E-ISSN | 1735-2428 |
| CiteScore | 4,9 |
| SJR | 0,389 |
| SNIP | 0,532 |