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For: Shirinzadeh H, Dilek E, Alım Z. Evaluation of Naphthalenylmethylen Hydrazine Derivatives as Potent Inhibitors on, Antiatherogenic Enzymes, Paraoxonase I and Acetylcholinesterase Activities. ChemistrySelect 2022;7. [DOI: 10.1002/slct.202104489] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 6.0] [Reference Citation Analysis]
Number Citing Articles
1 Wang S, Sun M, Ning Z, Chen Y, Zhou H, Mu W. The effects of sustained and diel-cycling hypoxia on high-latitude fish Phoxinus lagowskii. Comp Biochem Physiol Part D Genomics Proteomics 2023;45:101059. [PMID: 36706598 DOI: 10.1016/j.cbd.2023.101059] [Reference Citation Analysis]
2 Alım Z, Tunç T, Demirel N, Günel A, Karacan N. Synthesis of benzimidazole derivatives containing amide bond and biological evaluation as acetylcholinesterase, carbonic anhydrase I and II inhibitors. Journal of Molecular Structure 2022;1268:133647. [DOI: 10.1016/j.molstruc.2022.133647] [Reference Citation Analysis]
3 Bozbeymerde İ, Önel GT, Türkmenoğlu B, Gürsoy Ş, Dilek E. ( p ‐Chlorophenyl)‐3(2 H )pyridazinone Derivatives: Synthesis, in Silico , and AChE/BChE Inhibitory Activity. ChemistrySelect 2022;7. [DOI: 10.1002/slct.202202446] [Reference Citation Analysis]
4 Merde İB, Önel GT, Türkmenoğlu B, Gürsoy Ş, Dilek E. Pyridazinones containing the (4-methoxyphenyl)piperazine moiety as AChE/BChE inhibitors: design, synthesis, in silico and biological evaluation. Med Chem Res. [DOI: 10.1007/s00044-022-02968-x] [Reference Citation Analysis]
5 Korkmaz A, Kurtay G, Kaya E, Bursal E. Design, synthesis, spectroscopic characterizations, in vitro pancreatic lipase as well as tyrosinase inhibition evaluations and in silico analysis of novel aryl sulfonate-naphthalene hybrids. J Biomol Struct Dyn 2022;:1-16. [PMID: 36069113 DOI: 10.1080/07391102.2022.2116600] [Reference Citation Analysis]
6 Korkmaz IN, Türkeş C, Demir Y, Öztekin A, Özdemir H, Beydemir Ş. Biological evaluation and in silico study of benzohydrazide derivatives as paraoxonase 1 inhibitors. J Biochem Mol Toxicol 2022;:e23180. [PMID: 35916346 DOI: 10.1002/jbt.23180] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
7 Korkmaz IN, Türkeş C, Demir Y, Özdemir H, Beydemir Ş. Methyl benzoate derivatives: in vitro Paraoxonase 1 inhibition and in silico studies. J Biochem Mol Toxicol 2022;:e23152. [PMID: 35708184 DOI: 10.1002/jbt.23152] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]