schiff base journal

Band-shape analysis of electronic spectra and study of the hydrolysis of the Schiff bases of 5′-deoxypyridoxal and n-hexylamine in aqueous and non-aqueous media. This article is cited by Costantino Salerno, Andrea Lucano, Paolo Fasella. Base of Pyridoxal 5′-Phosphate and Leucine in Water Media with Cationic Surfactants.

Electrochemical behaviour of pyridoxal-5′-phosphate Schiff base with n-hexylamine. Kinetic Study on Stability of <> Spectroscopic studies of quinonoid species from pyridoxal 5'-phosphate. The analgesic effect of 26k (68.66%) was found to be better than that of diclofenac sodium (64.65%) [44].

A combined computational and experimental study on the hydrogen bonding with chloride ion in a crab-claw like site of a new chromium Schiff base complex. M.Angeles García del Vado, M.Piedad Martín Pérez, Angel F. Rodríguez Cardona, Gerardo R. Echevarría, JoséG. Stability of Biologically Active Pyridoxal and Pyridoxal Phosphate in the Presence of Lysine. Synthesis, protonation constants and biological activity determination of amino acid–salicylaldehyde-derived Schiff bases. Gregoria Cambr�n, Jos� M. Sevilla, Teresa Pineda, Manuel Bl�zquez. Mahmoud Zendehdel, Narges Yaghoobi Nia, Mojtaba Nasr-Esfahani, Pooria Farahani, Mohamad Reza Karbaschi. From the observed results it was concluded that a free phenol group containing compounds 27c, 27g, and 27h exhibited more potent activity than the other test compounds [45]. Find more information about Crossref citation counts.

Kinetic study. Carmen Hidalgo, Teresa Pineda, Jose M. Sevilla, Manuel Blázquez.

Synthesized compounds were evaluated for in vivo antidepressant and nootropic activities. Spectral regression and correlation coefficients of some benzaldimines and salicylaldimines in different solvents. More O'Ferrall, Brian A. Murray. Reaction of 2-acetyl-indane-1,3-dione with aniline - Schiff base or enamine?. Yathirajan, B. Narayana, B.K.

A series of 3-(benzylideneamino)-2-phenylquinazoline-4(3H)-one, 34(a–l) (Figure 31) was synthesized and evaluated for their cytotoxicity and antiviral activity. Minimum inhibitory concentration (MIC) along with ergosterol composition assay against C. albicans (ATCC 10261), C. glabrata (ATCC 90030), and C. tropicalis (ATCC 750) was performed. 1-Aminocyclopropanephosphonate: time-dependent inactivation of 1-aminocyclopropanecarboxylate deaminase and Bacillus stearothermophilus alanine racemase by slow dissociation behavior. A series of twenty-seven bis-Schiff base of isatin, 39(i–xxvii) (Figure 35) was synthesized and evaluated for their in vitro antiglycation activity.

Synthesis, spectroscopic properties and biological evaluation of transition metal complexes of salicylhydrazone of anthranilhydrazide: X-ray crystal structure of copper complex. This review reflects the contribution of Schiff bases to the design and development of novel lead having potential biological activities with fewer side effects. These metrics are regularly updated to reflect usage leading up to the last few days. Shoair, A.R. Andrei L. Osterman,, Harold B. Brooks,, Josep Rizo, and. Schiff bases have been utilized as synthons in the preparation of a number of industrial and biologically active compounds like formazans, 4-thiazolidinines, benzoxazines, and so forth, via ring closure, cycloaddition, and replacement reactions [23]. -phosphate schiff bases with dodecylamine and amino acids. M. A. Vazquez, F. Muñoz, J. Donoso, F. García Blanco. Selected compounds were screened for their in vitro anticancer and antifungal activities.

Aspartate .beta.-decarboxylase from Alcaligenes faecalis: carbon-13 kinetic isotope effect and deuterium exchange experiments.

Kinetics of the formation and hydrolysis of the Schiff bases of pyridoxal 5′-phosphate and copolypeptides containing l-lysine and aromatic l-amino acids. Teresa Dziembowska, Zbigniw Rozwadowski, Jerzy Sitkowski, Lech Stefaniak, Bogdan Brzeziński. David E. Metzler, Carol M. Metzler, Jayati Mitra. Schiff bases exhibit useful biological activities such anti-inflammatory, analgesic, antimicrobial, anticonvulsant, antitubercular, anticancer, antioxidant, anthelmintic, antiglycation, and antidepressant activities.

Please reconnect. Indian adult earthworms (P. posthuma) were employed for the anthelmintic activity. Isabel M. Plaza del Pino, Jose M. Sanchez-Ruiz. A.L.

Schiff bases of 5'-deoxypyridoxal with n-hexylamine in water-dioxane mixtures: influence of polarity of the medium on the catalysis of formation. An electrochemical and spectroscopic contribution. Kinetic properties and thermal stabilities of mutant forms of mitochondrial aspartate aminotransferase. Although all the compounds possessed activity against M. incognita, N-hexyl-2-hydroxyacetophenonimine (15j), N-hexyl-2-hydroxypropiophenonimine (15k), and N-propyl-2-hydroxypropiophenonimine (15l) were found to possess significant activity with LC50 values of 99.60, 74.46, 109.53, and mgL−1, respectively, as compared to other imines. Spectroscopic and kinetic evidence for a cyclic geminal diamine intermediate in the reaction of O-aminoserine with pyridoxal 5′-phosphate in alkali. Robert David Scott, Yen Chung Chang, Donald J. Graves, and David E. Metzler. The results revealed that the compounds 13a, 13e, and 13i displayed significant lowering of total cholesterol, phospholipids, and triglycerides in the plasma.

The common Schiff base are crystalline solids, which are feebly basic but at least some form insoluble salts with strong acids. CHEKHOV. Walters, T.J. Cornish, H.W. One-bond deuterium isotope effects on 15N chemical shifts in Schiff bases. Studies of 6-fluoropyridoxal and 6-fluoropyridoxamine 5'-phosphates in cytosolic aspartate aminotransferase. Studies on biologically active acylhydrazones.

Some novel Schiff bases, macrocyclic tetradentate nitrogen donor (N4) 6,7,14,15-tetrahydroxy-1,4,9,12-tetraazacyclohexadecane-5,8,13,16-tetrone ligand-based metal complexes, 11, (Figure 11) from 10, (Figure 10) were synthesized and screened for the in vitro antifungal activity and toxicity studies. Peter Kovacic, James R. Ames, Edward C. Taylor, Michael D. Ryan. L.S. B. Thomas, R. K. Nanda, L. P. Kothapalli, and S. C. Hamane, “Synthesis and biological evaluation of Schiff’s bases and 2-azetidinones of isonicotinyl hydrazone as potential antidepressant and nootropic agents,”, M. A. Bhat and M. A. Al-Omar, “Synthesis, characterization and in vivo anticonvulsant and neurotoxicity screening of Schiff bases of phthalimide,”, A. This review reflects the contribution of Schiff bases to the design and development of novel lead having potential biological activities with fewer side effects.

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