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Article detail · 2018

A Study On Synthesis, Biological Activities and Molecular Modelling of Some Novel Trisubstituted 1,2,4-Triazole Derivatives

Journal

ChemistrySelect

ISSN 2365-6549

YÖKSİS OpenAlex SJR Q2 JCR Q3 Citations 19 Percentile 76.9% FWCI 1.26
Year
2018
Type
article

Data source split

  • YÖKSİS YÖKSİS article record
  • YÖKSİS venue ChemistrySelect
  • Catalog match (ISSN) ChemistrySelect
  • OpenAlex OpenAlex enrichment (abstract, citations, topics)

Abstract

OpenAlex · English

Abstract In this study, 1‐(4‐substitued benzyl)‐3,5‐diphenyl‐ 1H ‐1,2,4‐triazoles ( 2 a‐e ) and ethyl(3,5‐diphenyl‐ 1H ‐1,2,4‐triazole‐1‐yl)acetate ( 3 ) were synthesized starting from 3,5‐diphenyl‐ 1H ‐1,2,4‐triazole ( 1 ). The ethyl acetate derivative ( 3 ) was converted to 2‐(3,5‐diphenyl‐ 1H ‐1,2,4‐triazole‐1‐yl)acetohydrazide ( 4 ) in ethanolic medium with hydrazine hydrate. The reaction of the acetohydrazide ( 4 ) with suitable isothiocyanates generate 2‐[(3, 5‐diphenyl‐ 1H ‐1,2,4‐triazole‐1‐yl)acetyl]‐4‐methyl/phenyhlthiosemicarbazide ( 5 a,b ). The cyclization of the thiosemicarbazide ( 5 a,b ) in the presence of NaOH (2 M) resulted in the formation of 5‐[(3, 5‐diphenyl‐ 1H ‐1,2,4‐triazole‐1‐yl)methyl]‐4‐methyl/phenyl‐2,4‐dihidro‐3H‐1,2,4‐triazole‐3‐thiol ( 6 a,b ). Finally, the synthesized 1,2,4‐triazole‐3‐thiols ( 6 a,b ) were converted to their S‐ substituebenzyl derivatives ( 7 a‐j ). All of the synthesized compounds ( 1‐7 ) were also examined for antioxidant capacities, and antiurease and anti‐acetylcholinesterase (anti‐AChE) activities. It has been found that antioxidant capacity and anti‐urease activity of the compound 7 f is very good in biochemically active compounds.

Topics

Citations

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

19 citations

OpenAlex cited_by_count (cache / database)

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

  1. Monoamine oxidase A and B inhibitory activities of 3,5-diphenyl-1,2,4-triazole substituted [1,2,4]triazolo[3,4-b][1,3,4]thiadiazole derivatives 2022 Citations 20 · OpenAlex
  2. Monoamine oxidase A and B inhibitory activities of 3,5-diphenyl-1,2,4-triazole substituted [1,2,4]triazolo[3,4-b][1,3,4]thiadiazole derivatives 2022 Citations 19 · OpenAlex
  3. Synthesis and kinetics studies of N ’xx-(2-(3,5-disubstituted-4H-1,2,4-triazol-4-yl)acetyl)-6/7/8-substituted-2-oxo-2H-chromen-3-carbohydrazide derivatives as potent antidiabetic agents 2019 Citations 19 · OpenAlex
  4. Synthesis and kinetics studies of N ’xx-(2-(3,5-disubstituted-4H-1,2,4-triazol-4-yl)acetyl)-6/7/8-substituted-2-oxo-2H-chromen-3-carbohydrazide derivatives as potent antidiabetic agents 2019 Citations 19 · OpenAlex
  5. Synthesis and kinetics studies of N′‐(2‐(3,5‐disubstituted‐4H‐1,2,4‐triazol‐4‐yl)acetyl)‐6/7/8‐substituted‐2‐oxo‐2H‐chromen‐3‐carbohydrazide derivatives as potent antidiabetic agents 2019 Citations 19 · OpenAlex
  6. Synthesis, In Vitro Evaluation, and Molecular Docking Studies of Novel 3,5‐Diphenyl‐1H‐1,2,4‐Triazole Derivatives as Potential hEGFR Inhibitors 2025 Citations 2 · OpenAlex
  7. Synthesis, In Vitro Evaluation, and Molecular Docking Studies of Novel 3,5‐Diphenyl‐1H‐1,2,4‐Triazole Derivatives as Potential hEGFR Inhibitors 2025 Citations 2 · OpenAlex
  8. Synthesis, In Vitro Evaluation, and Molecular Docking Studies of Novel 3,5‐Diphenyl‐1H‐1,2,4‐Triazole Derivatives as Potential hEGFR Inhibitors 2025 Citations 2 · OpenAlex
  9. Synthesis, In Vitro Evaluation, and Molecular Docking Studies of Novel 3,5‐Diphenyl‐1H‐1,2,4‐Triazole Derivatives as Potential hEGFR Inhibitors 2025 Citations 2 · OpenAlex

Authors

  1. ERGÜN GÜLTEKİN
  2. YAKUP KOLCUOĞLU KARADENİZ TEKNİK ÜNİVERSİTESİ
  3. ATİLLA AKDEMİR İSTANBUL KENT ÜNİVERSİTESİ
  4. YAKUP ŞİRİN
  5. HAKAN BEKTAŞ GİRESUN ÜNİVERSİTESİ
  6. OLCAY BEKİRCAN