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ŞÜKRÜ BEYDEMİR

PROFESÖR

ANADOLU ÜNİVERSİTESİ ECZACILIK FAKÜLTESİ TEMEL ECZACILIK BİLİMLERİ BÖLÜMÜ

  • Ana Dal Fen Bilimleri ve Matematik Temel Alanı
  • Yan Dal Kimya

Kayıtlı çıktılara kısa bakış — ayrıntılar aşağıda.

  • Makale 218
  • Proje 0
  • Kitap 1
  • Bildiri 188
  • Patent 0
  • Sanatsal 0
Scopus (SJR) Q1 42 Q2 119 Q3 21 Q4 3
WoS (JCR) Q1 39 Q2 74 Q3 48 Q4 23
TR Index 2 makale

Alan+yıl+tür normalize OpenAlex yüzdelik — Clarivate ESI / SciVal değildir.

Üst %1 makale 17
Üst %10 makale 115
Ort. yüzdelik 86.1%
Üst %1 payı 9.1%
Üst %10 payı 61.8%

Makaleler

YÖKSİS ve OpenAlex kaynak ayrımıyla makaleler; quartile ve TR Index ile daraltabilirsiniz.

Dizin filtreleri

Toplam 218 yayın

Scopus (SJR)
Q1 42 Q2 119 Q3 21 Q4 3
WoS (JCR)
Q1 39 Q2 74 Q3 48 Q4 23
TR Index
2 makale

Makale filtresi uygulandı. Filtreyi kaldır

Makale listesi

39 / 218 makale

  1. 2025 Esculetin attenuates doxorubicin-induced cardiac toxicity: Evidence from gene expression, enzyme activity, and molecular docking analyses Computational Biology and Chemistry DOI 10.1016/j.compbiolchem.2025.108654 YÖKSİS SJR Q2 JCR Q1 OpenAlex üst %1 OpenAlex 99.6%
  2. 2024 Bioactivity, cytotoxicity, and molecular modeling studies of novel sulfonamides as dual inhibitors of carbonic anhydrases and acetylcholinesterase Journal of Molecular Liquids DOI 10.1016/j.molliq.2024.125558 YÖKSİS SJR Q1 JCR Q1 OpenAlex üst %1 OpenAlex 99.2%
  3. 2024 The impact of some metals, molecular docking and molecular dynamic calculations on glucose 6-phosphate dehydrogenase activity in Capoeta trutta (Heckel, 1843) tissue Journal of Molecular Liquids DOI 10.1016/j.molliq.2024.124288 YÖKSİS SJR Q1 JCR Q1 OpenAlex üst %10 OpenAlex 98.0%
  4. 2024 Novel spiroindoline derivatives targeting aldose reductase against diabetic complications: Bioactivity, cytotoxicity, and molecular modeling studies Bioorganic Chemistry DOI 10.1016/j.bioorg.2024.107221 YÖKSİS SJR Q1 JCR Q1 OpenAlex üst %1 OpenAlex 99.7%
  5. 2023 Exploration of 1,2,3-triazole linked benzenesulfonamide derivatives as isoform selective inhibitors of human carbonic anhydrase BIOORGANIC & MEDICINAL CHEMISTRY DOI 10.1016/j.bmc.2022.117111 YÖKSİS SJR Q2 JCR Q1 OpenAlex üst %10 OpenAlex 98.4%
  6. 2023 Enzyme inhibition, molecular docking, and density functional theory studies of new thiosemicarbazones incorporating the 4‐hydroxy‐3,5‐dimethoxy benzaldehyde motif Archiv der Pharmazie DOI 10.1002/ardp.202200554 YÖKSİS SJR Q2 JCR Q1 OpenAlex üst %10 OpenAlex 97.3%
  7. 2023 Exploration of 1,2,3-triazole linked benzenesulfonamide derivatives as isoform selective inhibitors of human carbonic anhydrase BIOORGANIC & MEDICINAL CHEMISTRY DOI 10.1016/j.bmc.2022.117111 YÖKSİS SJR Q2 JCR Q1 OpenAlex üst %10 OpenAlex 98.4%
  8. 2023 A new series of hydrazones as small‐molecule aldose reductase inhibitors ARCHIV DER PHARMAZIE DOI 10.1002/ardp.202200570 YÖKSİS SJR Q2 JCR Q1 OpenAlex üst %10 OpenAlex 90.7%
  9. 2022 Synthesis, characterization and docking studies of benzenesulfonamide derivatives containing 1,2,3-triazole as potential ınhibitor of carbonic anhydrase I-II enzymes JOURNAL OF BIOMOLECULAR STRUCTURE & DYNAMICS DOI 10.1080/07391102.2022.2159531 YÖKSİS SJR Q2 JCR Q1 OpenAlex 66.8%
  10. 2022 Enzyme inhibition, molecular docking, and density functional theory studies of new thiosemicarbazones incorporating the 4‐hydroxy‐3,5‐dimethoxy benzaldehyde motif ARCHIV DER PHARMAZIE DOI 10.1002/ardp.202200554 YÖKSİS SJR Q2 JCR Q1 OpenAlex üst %10 OpenAlex 97.3%
  11. 2022 Design, synthesis, and biological activity of novel dithiocarbamate‐methylsulfonyl hybrids as carbonic anhydrase inhibitors Archiv der Pharmazie DOI 10.1002/ardp.202200132 YÖKSİS SJR Q2 JCR Q1 OpenAlex üst %10 OpenAlex 97.5%
  12. 2022 Exploration of 1,2,3-triazole linked benzenesulfonamide derivatives as isoform selective inhibitors of human carbonic anhydrase BIOORGANIC & MEDICINAL CHEMISTRY DOI 10.1016/j.bmc.2022.117111 YÖKSİS SJR Q2 JCR Q1 OpenAlex üst %10 OpenAlex 98.4%
  13. 2021 Novel inhibitors with sulfamethazine backbone: synthesis and biological study of multi-target cholinesterases and α-glucosidase inhibitors Journal of Biomolecular Structure and Dynamics DOI 10.1080/07391102.2021.1916599 YÖKSİS SJR Q2 JCR Q1 OpenAlex üst %1 OpenAlex 99.1%
  14. 2021 Design, synthesis, characterization, in vitro and in silico evaluation of novel imidazo[2,1-b][1,3,4]thiadiazoles as highly potent acetylcholinesterase and non-classical carbonic anhydrase inhibitors Bioorganic Chemistry DOI 10.1016/j.bioorg.2021.105009 YÖKSİS SJR Q2 JCR Q1 OpenAlex üst %10 OpenAlex 98.2%
  15. 2021 Molecular docking and inhibition studies of vulpinic, carnosic and usnic acids on polyol pathway enzymes Journal of Biomolecular Structure and Dynamics DOI 10.1080/07391102.2021.1967195 YÖKSİS SJR Q2 JCR Q1 OpenAlex üst %1 OpenAlex 99.7%
  16. 2021 Identification of a new class of potent aldose reductase inhibitors: Design, microwave-assisted synthesis, in vitro and in silico evaluation of 2-pyrazolines Chemico-Biological Interactions DOI 10.1016/j.cbi.2021.109576 YÖKSİS SJR Q1 JCR Q1 OpenAlex üst %10 OpenAlex 97.2%
  17. 2021 Biological effects of bis-hydrazone compounds bearing isovanillin moiety on the aldose reductase Bioorganic Chemistry DOI 10.1016/j.bioorg.2021.105473 YÖKSİS SJR Q2 JCR Q1 OpenAlex üst %10 OpenAlex 97.8%
  18. 2020 Synthesis, characterization and carbonic anhydrase I and II inhibitory evaluation of new sulfonamide derivatives bearing dithiocarbamate European Journal of Medicinal Chemistry DOI 10.1016/j.ejmech.2020.112392 YÖKSİS SJR Q1 JCR Q1 OpenAlex 55.5%
  19. 2020 Synthesis, characterization, inhibition effects, and molecular docking studies as acetylcholinesterase, ?-glycosidase, and carbonic anhydrase inhibitors of novel benzenesulfonamides incorporating 1,3,5-triazine structural motifs BIOORGANIC CHEMISTRY DOI 10.1016/j.bioorg.2020.103897 YÖKSİS SJR Q2 JCR Q1 OpenAlex üst %10 OpenAlex 98.8%
  20. 2020 Design, synthesis, in vitro and in silico investigation of aldose reductase inhibitory effects of new thiazole-based compounds Bioorganic Chemistry DOI 10.1016/j.bioorg.2020.104110 YÖKSİS SJR Q2 JCR Q1 OpenAlex üst %10 OpenAlex 97.2%

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