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Makale detayı · 2018 · article

Evaluation of chalcones as inhibitors of glutathione S-transferase

YÖKSİS OpenAlex SJR Q2 JCR Q2 Üst %10
Yıl2018
Atıf74OpenAlex
Yüzdelik%91,8
FWCI2,811,00 = dünya ortalaması
Scopus (SJR)Q2
WoS (JCR)Q2

Veri kaynağı ayrımı

  • YÖKSİSYÖKSİS makale kaydı
  • YÖKSİS dergi adıJOURNAL OF BIOCHEMICAL AND MOLECULAR TOXICOLOGY
  • Katalog eşleşmesi (ISSN)Journal of Biochemical and Molecular Toxicology
  • OpenAlexOpenAlex zenginleştirmesi (özet, atıf, konular)

Özet

OpenAlex İngilizce

Abstract Glutathione S‐transferases (GSTs) are the superfamily of multifunctional detoxification isoenzymes and play an important role in cellular signaling. In the present study, potential inhibition effects of chalcones were tested against human GST. For this purpose, GST was purified from human erythrocytes with 5.381 EU⋅mg−1 specific activity and 51.95% yield using a GSH–agarose affinity chromatographic method. The effects of chalcones on in vitro GST activity were tested at various concentrations. Ki constants of chalcones were found in the range of 7.76–41.93 μM. According to the results, 4‐fluorochalcone showed a better inhibitory effect compared with the other compounds. The inhibition mechanisms of 2'‐hydroxy‐4‐methoxychalcone and 4‐methoxychalcone were noncompetitive, whereas the inhibition mechanisms of 4'‐ hydroxychalcone, 4‐ fluorochalcone, and 4,4'‐ diflurochalcone were competitive.

Konular

Atıflar

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74atıfOpenAlex · cited_by_count (önbellek / veritabanı)

Yerel katalogda bu makaleye atıf yapan 128 yayın (OpenAlex referans eşleşmesi; tam dünya listesi değildir).

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  3. 2018 Diarylmethanon, bromophenol and diarylmethane compounds: Discovery of potent aldose reductase, α-amylase and α-glycosidase inhibitors as new therapeutic approach in diabetes and functional hyperglycemiaAtıf 211 · OpenAlex
  4. 2018 Diarylmethanon, bromophenol and diarylmethane compounds: Discovery of potent aldose reductase, alpha-amylase and alpha-glycosidase inhibitors as new therapeutic approach in diabetes and functional hyperglycemiaAtıf 211 · OpenAlex
  5. 2018 Diarylmethanon, bromophenol and diarylmethane compounds: Discovery of potent aldose reductase, α-amylase and α-glycosidase inhibitors as new therapeutic approach in diabetes and functional hyperglycemiaAtıf 211 · OpenAlex
  6. 2018 Diarylmethanon, bromophenol and diarylmethane compounds: Discovery of potent aldose reductase, α-amylase and α-glycosidase inhibitors as new therapeutic approach in diabetes and functional hyperglycemiaAtıf 211 · OpenAlex
  7. 2018 Diarylmethanon, bromophenol and diarylmethane compounds: Discovery of potent aldose reductase, α-amylase and α-glycosidase inhibitors as new therapeutic approach in diabetes and functional hyperglycemiaAtıf 211 · OpenAlex
  8. 2019 Synthesis, biological evaluation and in silico studies of novel N-substituted phthalazine sulfonamide compounds as potent carbonic anhydrase and acetylcholinesterase inhibitorsAtıf 136 · OpenAlex
  9. 2019 Antidiabetic properties of dietary phenolic compounds: Inhibition effects on α‐amylase, aldose reductase, and α‐glycosidaseAtıf 135 · OpenAlex
  10. 2019 Synthesis, biological evaluation and in silico studies of novel N-substituted phthalazine sulfonamide compounds as potent carbonic anhydrase and acetylcholinesterase inhibitorsAtıf 135 · OpenAlex

Yazarlar

5
  1. Muhammet Serhat Özaslan ARDAHAN ÜNİVERSİTESİ 1
  2. YELİZ DEMİR 2
  3. Hatice Esra Aslan 3
  4. ŞÜKRÜ BEYDEMİR ANADOLU ÜNİVERSİTESİ 4
  5. ÖMER İRFAN KÜFREVİOĞLU 5