Synthesis, carbonic anhydrase I and II inhibition studies of the 1,3,5-trisubstituted-pyrazolines

Article Properties
  • Language
    English
  • Publication Date
    2016/10/24
  • Indian UGC (journal)
  • Refrences
    28
  • Citations
    90
  • Halise Inci Gul Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Ataturk University, Erzurum, Turkey;
  • Ebru Mete Department of Chemistry, Faculty of Science, Ataturk University, Erzurum, Turkey;
  • Parham Taslimi Department of Chemistry, Faculty of Science, Ataturk University, Erzurum, Turkey;
  • Ilhami Gulcin Department of Chemistry, Faculty of Science, Ataturk University, Erzurum, Turkey;Department of Zoology, College of Science, King Saud University, Riyadh, Saudi Arabia; ORCID (unauthenticated)
  • Claudiu T. Supuran Neurofarba Department, Sezione di Scienze Farmaceutiche e Nutraceutiche, Università degli Studi di Firenze, Sesto Fiorentino, Florence, Italy
Cite
Gul, Halise Inci, et al. “Synthesis, Carbonic Anhydrase I and II Inhibition Studies of the 1,3,5-Trisubstituted-Pyrazolines”. Journal of Enzyme Inhibition and Medicinal Chemistry, vol. 32, no. 1, 2016, pp. 189-92, https://doi.org/10.1080/14756366.2016.1244533.
Gul, H. I., Mete, E., Taslimi, P., Gulcin, I., & Supuran, C. T. (2016). Synthesis, carbonic anhydrase I and II inhibition studies of the 1,3,5-trisubstituted-pyrazolines. Journal of Enzyme Inhibition and Medicinal Chemistry, 32(1), 189-192. https://doi.org/10.1080/14756366.2016.1244533
Gul HI, Mete E, Taslimi P, Gulcin I, Supuran CT. Synthesis, carbonic anhydrase I and II inhibition studies of the 1,3,5-trisubstituted-pyrazolines. Journal of Enzyme Inhibition and Medicinal Chemistry. 2016;32(1):189-92.
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A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding Analytical Biochemistry
  • Science: Chemistry: Organic chemistry: Biochemistry
  • Science: Biology (General)
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  • Science: Biology (General)
  • Science: Chemistry: Organic chemistry: Biochemistry
  • Science: Biology (General)
  • Science: Chemistry: Organic chemistry: Biochemistry
181,650 1976
In vitro inhibition of salicylic acid derivatives on human cytosolic carbonic anhydrase isozymes I and II Bioorganic & Medicinal Chemistry
  • Science: Biology (General)
  • Medicine: Therapeutics. Pharmacology
  • Science: Chemistry: Organic chemistry
  • Science: Chemistry: Analytical chemistry
  • Science: Chemistry
142 2008
Citations
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Citations Analysis
The category Science: Biology (General) 48 is the most commonly referenced area in studies that cite this article. The first research to cite this article was titled Synthesis and investigation of the conversion reactions of pyrimidine‐thiones with nucleophilic reagent and evaluation of their acetylcholinesterase, carbonic anhydrase inhibition, and antioxidant activities and was published in 2017. The most recent citation comes from a 2024 study titled Synthesis, characterization, and computational study of novel carvacrol-based 2-aminothiol and sulfonic acid derivatives as metabolic enzyme inhibitors. This article reached its peak citation in 2019, with 21 citations. It has been cited in 29 different journals, 10% of which are open access. Among related journals, the Journal of Biochemical and Molecular Toxicology cited this research the most, with 19 citations. The chart below illustrates the annual citation trends for this article.
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