| Makale Türü | Özgün Makale (SSCI, AHCI, SCI, SCI-Exp dergilerinde yayınlanan tam makale) | ||
| Dergi Adı | Molecular Diversity (Q2) | ||
| Dergi ISSN | 1381-1991 Wos Dergi Scopus Dergi | ||
| Dergi Tarandığı Indeksler | SCI-Expanded | ||
| Makale Dili | Türkçe | Basım Tarihi | 12-2026 |
| Cilt / Sayı / Sayfa | 0 / 1 / – | DOI | 10.1007/s11030-025-11418-w |
| Makale Linki | https://doi.org/10.1007/s11030-025-11418-w | ||
| UAK Araştırma Alanları |
Fen Bilimleri ve Matematik
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| Özet |
| In this study, ten novel dibromodibenzoazepine-substituted triazole hybrid compounds (AZ1–AZ10) were designed via a molecular hybridization approach and synthesized using click chemistry methodology. In the synthesis, the dibromodibenzoazepine derivative (12) was initially synthesized via bromination. Subsequent propargylation yielded the key intermediate, dibromodibenzoazepine-propargyl derivative (13). The Cu (I)-catalyzed azide-alkyne cycloaddition (CuAAC) reaction of propargyl derivative (13) with various substituted azide derivatives afforded the target hybrid compounds in high yields. The structures of these compounds were characterized using various spectroscopic techniques, including 1 H NMR, 13 C NMR, and MS. Among the synthesized compounds, AZ9 was determined to have the highest cytotoxicity on breast and colon cancer cell lines, including BT20, MCF7, MDA-MB-231, and HT29 … |
| Anahtar Kelimeler |
| Anticancer | Click chemistry | Dibenzoazepine | MD simulation | Triazole |
| Dergi Adı | MOLECULAR DIVERSITY |
| Yayıncı | Springer Nature |
| Açık Erişim | Hayır |
| ISSN | 1381-1991 |
| E-ISSN | 1573-501X |
| CiteScore | 8,5 |
| SJR | 0,646 |
| SNIP | 1,101 |