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Article detail · 2022 · article

Biological effects and molecular docking studies of Catechin 5-O-gallate: antioxidant, anticholinergics, antiepileptic and antidiabetic potentials

YÖKSİS OpenAlex Open access · green
Year2022
Citations32OpenAlex
Citations34Semantic Scholar · 1 influential
Percentile%82.7
FWCI1.641.00 = world average
Scopus (SJR)Q2
WoS (JCR)Q1

Data source split

  • YÖKSİSYÖKSİS article record
  • YÖKSİS venueJOURNAL OF BIOMOLECULAR STRUCTURE & DYNAMICS
  • Catalog match (ISSN)Journal of Biomolecular Structure and Dynamics
  • OpenAlexOpenAlex enrichment (abstract, citations, topics)
  • Semantic Scholarcitation count (not merged with OpenAlex)

Abstract

OpenAlex English

Gallocatechin gallate is a form of catechin and an ester of gallocatechin and gallic acid. This is an epimer of the gallate epigallocatechin. In this study, the effect of this molecule, containing a biologically active group, was investigated in terms of important metabolic enzymes (carbonic anhydrase isoenzymes I and II (hCA I and II), achethylcholinesterase (AChE) and α-glycosidase (α-Gly) enzymes). The molecular docking method used to compare the biological activities of the Catechin 5-O-gallate molecule against enzymes was used. Afterwards, the ADME/T analysis was performed to investigate the drug availability of the Catechin 5-O-gallate molecule and the parameters obtained from ADME/T analysis were examined. Continuation of this study, for evaluating antioxidant and radical scavenging capacity Catechin 5-O-gallate, cupric ion (Cu2+) reduction capacity by CUPRAC method, Fe3+-Fe2+ reducing capacity, DPPH free radical clarifying (DPPH·), ABTS radical clarifying (ABTS•+) were performed separately and during the study, trolox, α-tocopherol BHT and BHA were used as the reference antioxidant compound. Comparisons were applied with the four standard substances. Communicated by Ramaswamy H. Sarma

Topics

Citations

OpenAlex cited_by_count. Not a WoS or Scopus citation count; those sources have no separate column here.

32citationsOpenAlex · cited_by_count (cache / database)

72 publications in the local catalog that cite this work (OpenAlex reference match; not the full global list).

  1. 2023 Synthesis and Evaluation of Quinazolin-4(3H)-one Derivatives as Multitarget Metabolic Enzyme Inhibitors: A Biochemistry-Oriented Drug DesignCitations 56 · OpenAlex
  2. 2023 Synthesis and Evaluation of Quinazolin‐4(3 H )‐one Derivatives as Multitarget Metabolic Enzyme Inhibitors: A Biochemistry‐Oriented Drug DesignCitations 56 · OpenAlex
  3. 2023 Synthesis and Evaluation of Quinazolin-4(3H)-one Derivatives as Multitarget Metabolic Enzyme Inhibitors: A Biochemistry-Oriented Drug DesignCitations 56 · OpenAlex
  4. 2022 Synthesis, carbonic anhydrase inhibitory activity, anticancer activity and molecular docking studies of new imidazolyl hydrazone derivativesCitations 54 · OpenAlex
  5. 2022 Synthesis, carbonic anhydrase inhibitory activity, anticancer activity and molecular docking studies of new imidazolyl hydrazone derivativesCitations 53 · OpenAlex
  6. 2022 Synthesis, carbonic anhydrase inhibitory activity, anticancer activity and molecular docking studies of new imidazolyl hydrazone derivativesCitations 53 · OpenAlex
  7. 2022 Synthesis, carbonic anhydrase inhibitory activity, anticancer activity and molecular docking studies of new imidazolyl hydrazone derivativesCitations 53 · OpenAlex
  8. 2022 Synthesis, carbonic anhydrase inhibitory activity, anticancer activity and molecular docking studies of new imidazolyl hydrazone derivativesCitations 53 · OpenAlex
  9. 2022 Synthesis, carbonic anhydrase inhibitory activity, anticancer activity and molecular docking studies of new imidazolyl hydrazone derivativesCitations 53 · OpenAlex
  10. 2022 1,2,3-Triazole substituted phthalocyanine metal complexes as potential inhibitors for anticholinesterase and antidiabetic enzymes with molecular docking studiesCitations 49 · OpenAlex

Authors

4
  1. PARHAM TASLIMI 1
  2. ÜMİT MUHAMMET KOÇYİĞİT 2
  3. BURAK TÜZÜN SİVAS CUMHURİYET ÜNİVERSİTESİ 3
  4. MAHİNUR KIRICI 4