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For: Yapar G, Esra Duran H, Lolak N, Akocak S, Türkeş C, Durgun M, Işık M, Beydemir Ş. Biological effects of bis-hydrazone compounds bearing isovanillin moiety on the aldose reductase. Bioorg Chem 2021;117:105473. [PMID: 34768205 DOI: 10.1016/j.bioorg.2021.105473] [Cited by in Crossref: 10] [Cited by in F6Publishing: 11] [Article Influence: 5.0] [Reference Citation Analysis]
Number Citing Articles
1 Ma C, Liu C, Ren M, Cui L, Xi X, Kang W. Inhibitory effect of quercetin-3-O-α-rhamnoside, p-coumaric acid, phloridzin and 4-O-β-glucopyranosyl-cis-coumaric acid on rats liver microsomes cytochrome P450 enzyme activities. Food Chem Toxicol 2023;172:113583. [PMID: 36577462 DOI: 10.1016/j.fct.2022.113583] [Reference Citation Analysis]
2 Altıntop MD, Demir Y, Türkeş C, Öztürk RB, Cantürk Z, Beydemir Ş, Özdemir A. A new series of hydrazones as small-molecule aldose reductase inhibitors. Arch Pharm (Weinheim) 2023;:e2200570. [PMID: 36603162 DOI: 10.1002/ardp.202200570] [Reference Citation Analysis]
3 Demir Y, Türkeş C, Çavuş MS, Erdoğan M, Muğlu H, Yakan H, Beydemir Ş. Enzyme inhibition, molecular docking, and density functional theory studies of new thiosemicarbazones incorporating the 4-hydroxy-3,5-dimethoxy benzaldehyde motif. Arch Pharm (Weinheim) 2022;:e2200554. [PMID: 36575148 DOI: 10.1002/ardp.202200554] [Reference Citation Analysis]
4 Türkeş C, Demir Y, Beydemir Ş. In Vitro Inhibitory Activity and Molecular Docking Study of Selected Natural Phenolic Compounds as AR and SDH Inhibitors**. ChemistrySelect 2022;7. [DOI: 10.1002/slct.202204050] [Reference Citation Analysis]
5 Yararli K, Ozer EB, Bayindir S, Caglayan C, Turkes C, Beydemir S. The synthesis, biological evaluation and in silico studies of asymmetric 3,5-diaryl-rhodanines as novel inhibitors of human carbonic anhydrase isoenzymes. Journal of Molecular Structure 2022. [DOI: 10.1016/j.molstruc.2022.134783] [Reference Citation Analysis]
6 Abbas A, Mehmood MHH, Muhammad F, Siddique R, Kamran AAM. Evaluation of the wound healing, anti-inflammatory, and antimicrobial activity of isovanillin by using an animal model.. [DOI: 10.21203/rs.3.rs-2114680/v1] [Reference Citation Analysis]
7 Lolak N, Akocak S, Durgun M, Duran HE, Necip A, Türkeş C, Işık M, Beydemir Ş. Novel bis-ureido-substituted sulfaguanidines and sulfisoxazoles as carbonic anhydrase and acetylcholinesterase inhibitors. Mol Divers 2022. [PMID: 36136229 DOI: 10.1007/s11030-022-10527-0] [Reference Citation Analysis]
8 Demir Y, Tokalı FS, Kalay E, Türkeş C, Tokalı P, Aslan ON, Şendil K, Beydemir Ş. Synthesis and characterization of novel acyl hydrazones derived from vanillin as potential aldose reductase inhibitors. Mol Divers. [DOI: 10.1007/s11030-022-10526-1] [Reference Citation Analysis]
9 Tabbiche A, Bouchama A, Chafai N, Zaidi F, Chiter C, Yahiaoui M, Abiza A. New bis hydrazone: Synthesis, X-ray crystal structure, DFT computations, conformational study and in silico study of the inhibition activity of SARS-CoV-2. J Mol Struct 2022;1261:132865. [PMID: 35345533 DOI: 10.1016/j.molstruc.2022.132865] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
10 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]
11 Kumar M, Kumar Singh P, Choudhary S, Silakari O. Hydantoin based dual inhibitors of ALR2 and PARP-1: Design, synthesis, in-vitro and in-vivo evaluation. Bioorganic Chemistry 2022. [DOI: 10.1016/j.bioorg.2022.106108] [Reference Citation Analysis]
12 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]