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akaturk Akademik ölçüm

Makale detayı · 2025

Discovery of Dual‐Inhibitor Acyl Hydrazones for Acetylcholinesterase and Carbonic Anhydrase I/II: A Mechanistic Insight into Alzheimers Disease

Dergi

ChemistrySelect

ISSN 2365-6549

YÖKSİS OpenAlex Açık erişim · green SJR Q3 JCR Q3 Atıf 10 Üst %10 Yüzdelik 92.7% FWCI 3.4
Yıl
2025
Tür
article

Veri kaynağı ayrımı

  • YÖKSİS YÖKSİS makale kaydı
  • YÖKSİS dergi adı ChemistrySelect
  • Katalog eşleşmesi (ISSN) ChemistrySelect
  • OpenAlex OpenAlex zenginleştirmesi (özet, atıf, konular)

Özet

OpenAlex · İngilizce

Abstract This study presents the synthesis of various non‐sulfonamide acyl hydrazone derivatives intended as multi‐target ligands for the treatment of Alzheimer's disease. The derivatives were thoroughly characterized using advanced spectroscopic techniques and their inhibitory activities against key enzymes, acetylcholinesterase (AChE) and human carbonic anhydrase I/II (hCA) were systematically assessed. The synthesized compounds demonstrated significant suppression of hCAs. The 4‐methoxycarbonyl compound ( 2a , Ki = 69.74 nM) exhibited a robust inhibitory effect against hCA I compared to the reference medication acetazolamide (AAZ, Ki = 373.46 nM). The 4‐dimethylamino compound ( 2b , K i of 120.36 nM) exhibited superior potency compared to AAZ (K i of 350.66 nM) against hCA II. 2,4‐dinitrobenzylidene ( 2n , K i of 69.18 nM) derivative displayed a remarkable inhibitory effect against AChE compared to tacrine (THA, K i of 205.78 nM). Additionally, in silico studies provided insight into the binding interactions enhancing the understanding of their multi‐target potential. This study identified compounds with varying affinities for hCA isoenzymes highlighting their potential as effective and selective hCA inhibitors. The reported compounds exhibited significant biological inhibitory potency indicating their potential as a promising lead compound against hCAs and AChE.

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Atıflar

OpenAlex cited_by_count. WoS veya Scopus atıf sayısı değildir; o kaynaklar için ayrı kolon yoktur.

10 atıf

OpenAlex cited_by_count (önbellek / veritabanı)

Yerel katalogda bu makaleye atıf yapan 9 yayın (OpenAlex referans eşleşmesi; tam dünya listesi değildir).

  1. Novel thiazolidinedione hybrids as cholinesterase inhibitors and targeting neuroblastoma: design, synthesis, in vitro and in silico biological evaluations 2025 Atıf 12 · OpenAlex
  2. Novel thiazolidinedione hybrids as cholinesterase inhibitors and targeting neuroblastoma: design, synthesis, in vitro and in silico biological evaluations. 2025 Atıf 12 · OpenAlex
  3. Synthesis of Thiazole-methylsulfonyl Derivatives, X-ray Study, and Investigation of Their Carbonic Anhydrase Activities: In Vitro and In Silico Potentials 2025 Atıf 7 · OpenAlex
  4. Synthesis of Thiazole-methylsulfonyl Derivatives, X-ray Study, and Investigation of Their Carbonic Anhydrase Activities: In Vitro and In Silico Potentials 2025 Atıf 7 · OpenAlex
  5. Synthesis of Thiazole-methylsulfonyl Derivatives, X-ray Study, and Investigation of Their Carbonic Anhydrase Activities: In Vitro and In Silico Potentials 2025 Atıf 7 · OpenAlex
  6. Synthesis of Thiazole-methylsulfonyl Derivatives, X-ray Study, and Investigation of Their Carbonic Anhydrase Activities: In Vitro and In Silico Potentials 2025 Atıf 7 · OpenAlex
  7. Synthesis of Thiazole-methylsulfonyl Derivatives, X-ray Study, and Investigation of Their Carbonic Anhydrase Activities: In Vitro and In Silico Potentials 2025 Atıf 7 · OpenAlex
  8. Investigation of the Phytochemical Composition, Antioxidant, and Anti‐Enzyme Activities of Hedlundia tamamschjanae and Hedlundia Roopiana From Erzurum, Türkiye 2026 Atıf 0 · OpenAlex
  9. Phenylsulfonylethyl‐Substituted Benzimidazolium Salts: Synthesis, Characterization, Crystal Structure, Molecular Docking, and Inhibitory Properties Against Various Enzymes 2026 Atıf 0 · OpenAlex

Yazarlar

  1. EFE DOĞUKAN DİNCEL
  2. EBRU DİDEM KURAN
  3. YELİZ DEMİR ARDAHAN ÜNİVERSİTESİ
  4. BİLGESU ONUR SUCU
  5. İLHAMİ GÜLÇİN ATATÜRK ÜNİVERSİTESİ
  6. NURAY GÜZELDEMİRCİ İSTANBUL ÜNİVERSİTESİ