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akaturk Akademik ölçüm

Makale detayı · 2022

Design, synthesis, and biological activity of novel dithiocarbamate‐methylsulfonyl hybrids as carbonic anhydrase inhibitors

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YÖKSİS OpenAlex SJR Q2 JCR Q1 Atıf 74 Üst %10 Yüzdelik 97.5% FWCI 5.77
Yıl
2022
ISSN
0365-6233
Tür
article

Veri kaynağı ayrımı

  • YÖKSİS YÖKSİS makale kaydı
  • OpenAlex OpenAlex zenginleştirmesi (özet, atıf, konular)

Özet

İngilizce (OpenAlex)

in their structure, can be easily inhibited by dithiocarbamate compounds. In addition, CA enzyme inhibitory activities are known in groups such as sulfonamide and methylsulfonyl. For this purpose, in this study, a series of 23 new dithiocarbamate-methylsulfonyl derivatives were synthesized and their CA enzyme inhibitory activities were investigated. The inhibition potentials of the obtained compounds against the human CA I and CA II enzymes were investigated by the in vitro enzyme isolation method. It is seen that the compounds show activity at the nanomolar level. Molecular docking studies of the compounds were carried out by in silico methods. The poses of compounds 2a, 2e, 2o, and 2t are presented.

Konular

  • Enzyme function and inhibition
  • Synthesis and Catalytic Reactions
  • Cholinesterase and Neurodegenerative Diseases

Birincil konu Enzyme function and inhibition

Yazarlar

  1. DERYA OSMANİYE
  2. CÜNEYT TÜRKEŞ
  3. YELİZ DEMİR
  4. YUSUF ÖZKAY
  5. ŞÜKRÜ BEYDEMİR ANADOLU ÜNİVERSİTESİ
  6. ZAFER ASIM KAPLANCIKLI