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Showing results for m kaboudin
Your search for M Kabudan retrieved no results
Water oxidation couples to electrocatalytic hydrogenation of carbonyl compounds and unsaturated carbon-carbon bonds by nickel.
Behrouzi L, Zand Z, Fotuhi M, Kaboudin B, Najafpour MM. Behrouzi L, et al. Sci Rep. 2022 Nov 19;12(1):19968. doi: 10.1038/s41598-022-23777-7. Sci Rep. 2022. PMID: 36402849 Free PMC article.
This reaction utilized inexpensive nickel foam electrodes (1 cm(2)) and LiClO(4) (0.05 M) as a commercially accessible electrolyte in an aqueous medium. Under electrochemical conditions, a series of alcohols (21 examples) produces high selectivity in good yields (up to 100 …
This reaction utilized inexpensive nickel foam electrodes (1 cm(2)) and LiClO(4) (0.05 M) as a commercially accessible electrolyte in …
Heteroleptic Silver(I) and Gold(I) N-Heterocyclic Carbene Complexes: Structural Characterization, Computational Analysis, Tyrosinase Inhibitory, and Biological Effects.
Neshat A, Mahdavi A, Yousefshahi MR, Cheraghi M, Eigner V, Kucerakova M, Dusek M, Rezaie F, Kaboudin B. Neshat A, et al. Inorg Chem. 2023 Oct 16;62(41):16710-16724. doi: 10.1021/acs.inorgchem.3c01759. Epub 2023 Oct 3. Inorg Chem. 2023. PMID: 37788161
Derivatization of (NHC)M-Cl (M = Ag, Au) with selected sulfur donors from the family of dialkyldithiophosphates and bis(2-mercapto-1-methylimidazolyl)borate ligands gave a series of heteroleptic mononuclear complexes. ...
Derivatization of (NHC)M-Cl (M = Ag, Au) with selected sulfur donors from the family of dialkyldithiophosphates and bis(2-merc …
Synthesis of α-oxycarbanilinophosphonates and their anticholinesterase activities: the most potent derivative is bound to the peripheral site of acetylcholinesterase.
Kaboudin B, Emadi S, Faghihi MR, Fallahi M, Sheikh-Hasani V. Kaboudin B, et al. J Enzyme Inhib Med Chem. 2013 Jun;28(3):576-82. doi: 10.3109/14756366.2012.663362. Epub 2012 Mar 7. J Enzyme Inhib Med Chem. 2013. PMID: 22397393 Free article.
Molecular modelling studies suggest that the most potent inhibitor (compound 4h, IC(50) = 6.36 M) is bound to the peripheral site of AChE, which suggests that it decreases the catalytic activity not through binding to the active site but through blocking the entrance of t …
Molecular modelling studies suggest that the most potent inhibitor (compound 4h, IC(50) = 6.36 M) is bound to the peripheral site of …