İçeriğe geç
akaturk Akademik ölçüm

Makale detayı · 2022

Some phenolic natural compounds as carbonic anhydrase inhibitors: An in vitro and in silico study

Dergi

Archiv der Pharmazie

ISSN 0365-6233

YÖKSİS OpenAlex Açık erişim · green SJR Q2 JCR Q1 Atıf 23 Yüzdelik 83.8% FWCI 1.66
Yıl
2022
Tür
article

Veri kaynağı ayrımı

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

Özet

OpenAlex · İngilizce

Abstract This paper presents experimental and molecular docking studies on the inhibitory effects of tyrosol, hydroxytyrosol, luteolin, diosmetin, caffeic acid, luteolin 7‐O‐glycoside, and apigenin 7‐O‐glycoside from olive (Olea europaea L.) leaf against human carbonic anhydrase (hCA, E.C.4.2.1.1) isozymes I and II. After these isozymes were separately purified, their activities were determined using the esterase activity. IC50 values for hCA I and II were calculated as 2.02–11.38 µM and 2.23–9.05 µM, respectively. The compounds were identified as CA inhibitors, with Ki values in the ranges of 1.66–9.17 µM for the hCA I isozyme and 1.49–14.21 µM for hCA II. The inhibitory effects of these natural compounds were also compared to acetazolamide, which is a potent inhibitor of both CA isozymes. Our results may contribute to the synthesis of new CA inhibitors and pave the way for new drug design in the treatment of a number of diseases including cancer, obesity, diabetes, and glaucoma.

Konular

Atıflar

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

23 atıf

OpenAlex cited_by_count (önbellek / veritabanı)

Yerel katalogda bu makaleye atıf yapan 24 yayın (OpenAlex referans eşleşmesi; tam dünya listesi değildir).

  1. Synthesis, characterization, molecular docking and in vitro anti-cancer activity studies of new and highly selective 1,2,3-triazole substituted 4-hydroxybenzohyrdazide derivatives 2023 Atıf 46 · OpenAlex
  2. Synthesis, characterization, molecular docking and in vitro anti-cancer activity studies of new and highly selective 1,2,3-triazole substituted 4-hydroxybenzohyrdazide derivatives 2023 Atıf 46 · OpenAlex
  3. Piperazine-2-carboxylic acid derivatives as MTDLs anti-Alzheimer agents: Anticholinesterase activity, mechanistic aspect, and molecular modeling studies 2024 Atıf 25 · OpenAlex
  4. Peripheral (E)‐2‐[(4‐hydroxybenzylidene)‐3,4‐dihydronaphthalen‐1(2H)‐one)]‐coordinated phthalocyanines with improved enzyme inhibition properties and photophysicochemical behaviors 2024 Atıf 25 · OpenAlex
  5. Peripheral (E)‐2‐[(4‐hydroxybenzylidene)‐3,4‐dihydronaphthalen‐1(2H)‐one)]‐coordinated phthalocyanines with improved enzyme inhibition properties and photophysicochemical behaviors 2024 Atıf 25 · OpenAlex
  6. A cadmium-thiocyanate coordination polymer with bridging 2-aminopyridine: Synthesis, characterization DFT studies, Hirshfeld Surface analysis and docking studies 2024 Atıf 25 · OpenAlex
  7. Synthesis, Characterization, Molecular Docking and in vitro Biological Studies of Thiazolidin-4-one Derivatives as Anti-Breast-Cancer Agents 2023 Atıf 22 · OpenAlex
  8. Synthesis, characterization, In vitro and In silico investigations of novel 1,2,3-triazole substituted salicylic acid phenolic hydrazones hybrids targeting TGF-β2 expression in colorectal carcinoma 2025 Atıf 20 · OpenAlex
  9. Synthesis, Characterization, In Vitro and In Silico Investigations of Novel 1,2,3-Triazole Substituted Salicylic Acid Phenolic-Hydrazones Hybrids Targeting TGF-β2 Expression in Colorectal Carcinoma 2025 Atıf 20 · OpenAlex
  10. Synthesis, characterization, In vitro and In silico investigations of novel 1,2,3-triazole substituted salicylic acid phenolic hydrazones hybrids targeting TGF-β2 expression in colorectal carcinoma 2025 Atıf 20 · OpenAlex

Yazarlar

  1. AHMET GÖKHAN AĞGÜL AĞRI İBRAHİM ÇEÇEN ÜNİVERSİTESİ
  2. NAİM UZUN AĞRI İBRAHİM ÇEÇEN ÜNİVERSİTESİ
  3. MÜSLÜM KUZU
  4. PARHAM TASLIMI BARTIN ÜNİVERSİTESİ
  5. İLHAMİ GÜLÇİN