Zobrazeno 1 - 10
of 13
pro vyhledávání: '"D. B. Rubinov"'
Synthesis and Cytotoxic Activity of Novel Chalcone Analogues with Pyridine-2,4(1Н,3Н)-dione Fragment
Autor:
T. S. Khlebniсova, D. B. Rubinov, A. V. Baranovsky, F. A. Lakhvich, F. S. Pashkovsky, T. V. Chukarina, S. E. Ogurtsova
Publikováno v:
Russian Journal of General Chemistry. 93:476-484
Publikováno v:
Applied Biochemistry and Microbiology. 44:19-27
Effect of 2-acylcyclohexane-1,3-dione derivatives (tralkoxydim and its diketone precursors) on peroxidase-catalyzed oxidation of 3,3′,5,5′-tetramethylbenzidine (TMB), o-phenylenediamine (PDA), and the phenol-4-aminoantipyrine (4-AAP) couple has b
Publikováno v:
Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy. 61:2161-2167
We have investigated the electron absorption, fluorescence and phosphorescence spectra of 8-azasteroids and model compounds containing enaminodicarbonyl fragment. It has been shown that the investigated compounds have absorption and phosphorescence s
Publikováno v:
Applied Biochemistry and Microbiology. 41:12-17
Competitive inhibition of soybean urease was studied at 36°C in aqueous solution (pH 4.95) in the presence of polycarbonyl compounds (PCCs): oxalyldihydrazide (ODH), its polydisulfide (poly(DSODH)), three cyclic β-triketones (CTKs), and seven cycli
Publikováno v:
Biochemistry (Moscow). 69:1344-1352
Competitive inhibition of soybean urease by 15 triketone oximes has been studied at 36°C in aqueous solution (pH 4.95). The studied oximes are supposed chelators for the nickel atom in the urease metallocenter. The inhibition constants of urea hydro
Publikováno v:
Applied Biochemistry and Microbiology. 40:337-344
Competitive inhibition of soybean urease by 11 cyclic β-triketones was studied in aqueous solutions at pH 7.4 and 36°C. This process was characterized quantitatively by the inhibition constant (Ki), which showed a strong dependence on the structure
Publikováno v:
Chemistry of Natural Compounds. 31:537-559
This review systematizes information on 2-acylcyclohexane-1,3-diones and 2-acylcyclopentane-1,3-diones isolated from natural sources. Questions of their biological and chemical synthesis, their natural functions, and the biological activity that they
Publikováno v:
ChemInform. 24
The reaction of cyclohexane Β-triketones with 6-hydrazinophenanthridine gave enehydrazinodiketones, which were cyclized upon heating to give derivatives of 1-(phenanthridin-6′-yl)-4,5,6,7-tetrahydroindazole.
Publikováno v:
Chemistry of Heterocyclic Compounds. 28:1385-1388
The reaction of cyclohexane Β-triketones with 6-hydrazinophenanthridine gave enehydrazinodiketones, which were cyclized upon heating to give derivatives of 1-(phenanthridin-6′-yl)-4,5,6,7-tetrahydroindazole.
Publikováno v:
Prikladnaia biokhimiia i mikrobiologiia. 44(1)
Effect of 2-acylcyclohexane-1,3-dione derivatives (tralkoxydim and its diketone precursors) on peroxidase-catalyzed oxidation of 3,3',5,5'-tetramethylbenzidine (TMB), o-phenylenediamine (PDA), and the phenol-4-aminoantipyrine (4-AAP) couple has been