Phytochemical profiling and evaluation of modified resazurin microtiter plate assay of the roots of Trillium govanianum

Abstract

Trillium govanianum Wall. ex D. Don (Melanthiaceae alt. Trilliaceae), is native to the Himalayas. The present study, for the first time, was undertaken to explore the antimicrobial potential, to determine the minimum inhibitory concentration (MIC) values of the methanol extract of the roots of Trillium govanianum and its solid phase extraction (SPE) fractions by using resazurin microtiter assay (REMA) against Gram positive and Gram negative bacterial registered strains and to carry out phytochemical analysis. The remarkable amount of gallic acid equivalent phenolic and quercetin equivalent flavonoid content was manifested by MeOH extract (20.27?±?3.03?mg GAE/g DW and 9.25?±?0.50?mg QE/g DW respectively). The GC/MS analysis revealed the presence saturated and unsaturated components. Considerable level of antibacterial potential against Gram-positive bacteria (MIC: 2.5-0.009?mg/mL) than against Gram-negative bacteria (MIC: 2.5-0.165?mg/mL) were observed. The use of microtiter plates has the advantage of lower cost, fast and quantitative results.     

Theoretical studies of structural and magnetic properties of cubic perovskites PrCoO3 and NdCoO3

The structural and magnetic properties of cubic perovskites, PrCoO₃ and NdCoO₃, are studied using the full potential linearized augmented plane wave (FP-LAPW) method within the frame work of density functional theory (DFT). The structural parameters are also investigated by analytical techniques. The calculated structural parameters are consistent with the experimental results. The strong hybridization of the O-2p, Co-3d and Pr/Nd-4 f states around the Fermi level reveals that these compounds are metallic. It is also found that the origin of ferromagnetism in these compounds is double-exchange interaction between Co-3d states via O-2p states (Co-O-Co).     

Using conformationally locked nucleosides to calibrate the anomeric effect: Implications for glycosyl bond stability

Steric and electronic parameters, such as the anomeric effect (AE) and gauche effect play significant roles in steering the North⇆South equilibrium of nucleosides in solution.Two isomeric oxa-bicyclo[3.1.0]hexane nucleosides that are conformationally locked in either the North or the South conformation of the pseudorotational cycle were designed to study the consequences of having the AE operational or not, independent of other parameters. The rigidity of the system allowed the orientation of the orbitals involved to be set in ‘fixed’ relationships, either antiperiplanar where the AE is permanently ‘on’, or gauche where the AE is impaired. The consequences of these two alternatives were subjected to high-level calculations and measured experimentally by X-ray crystallography, hydrolytic stability of the glycosyl bond, and pK_a values.     

Production from ilmenite of TiO2-supported catalysts for selective catalytic reduction of NO with NH3

Economic production of titanium dioxide (yield >98 %) from ilmenite has been achieved by use of a modified sulfate reduction process. A series of samples were prepared by varying the concentration of titanium dioxide nuclei (0.2, 0.3, and 0.6 %) and further impregnation with antimony and vanadia. The structural and acidic properties of the samples were comprehensively studied by X-ray diffraction (XRD), transmission electron microscopy, BJH pore size distribution, and temperature-programmed desorption of NH₃. The XRD results revealed the presence of intense peaks from anatase titanium dioxide. Enhancement of surface area was observed for second-time filtered samples, possibly because of loss of iron from the bulk. As a result, formation of additional micropores was apparent from N₂ adsorption and desorption isotherms. Among all the antimony and vanadia-doped samples, the first-time filtered sample with the low concentration of nuclei (0.2 %) had the highest catalytic activity at low temperatures, owing to its larger pore size and abundant acidic species.     

Metachronal propulsion of non-Newtonian viscoelastic mucus in an axisymmetric tube with ciliated walls

Cilia-induced flow of viscoelastic mucus through an idealized two-dimensional model of the human trachea is presented.The cilia motion is simulated by a metachronal wave pattern which enables the mobilization of highly viscous mucus even at nonzero Reynolds numbers.The viscoelastic mucus is analyzed with the upper convected Maxwell viscoelastic formulation which features a relaxation time and accurately captures normal stress generation in shear flows.The governing equations are transformed from fixed to wave(laboratory)frame with appropriate variables and resulting differential equations are perturbed about wave number.The trachea is treated as an axisymmetric ciliated tube.Radial and axial distributions in axial velocity are calculated via the regular perturbation method and pressure rise is computed with numerical integration using symbolic software MATHEMATICA^‘TM’.The influence of selected parameters which is cilia length,and Maxwell viscoelastic material parameter i.e.relaxation time for prescribed values of wave number are visualized graphically.Pressure rise is observed to increase considerably with elevation in both cilia length and relaxation time whereas the axial velocity is markedly decelerated.The simulations provide some insight into viscous-dominated cilia propulsion of rheological mucus and also serve as a benchmark for more advanced modeling.     

Comprehensive structural studies of 2',3'-difluorinated nucleosides: comparison of theory, solution, and solid state

The conformations of three 2',3'-difluoro uridine nucleosides were studied by X-ray crystallography, NMR spectroscopy, and ab initio calculations in an attempt to define the roles that the two vicinal fluorine atoms play in the puckering preferences of the furanose ring. Two of the compounds examined contained fluorine atoms in either the arabino or xylo dispositions at C2' and C3' of a 2',3'-dideoxyuridine system. The third compound also incorporated fluorine atoms in the xylo configuration on the furanose ring but was substituted with a 6-azauracil base in place of uracil. A battery of NMR experiments in D 2O solution was used to identify conformational preferences primarily from coupling constant and NOE data. Both (1)H and (19)F NMR data were used to ascertain the preferred sugar pucker of the furanose ring through the use of the program PSEUROT. Compound-dependent parameters used in the PSEUROT calculations were newly derived from complete sets of conformations calculated from high-level ab initio methods. The solution and theoretical data were compared to the conformations of each molecule in the solid state. It was shown that both gauche and antiperiplanar effects may be operative to maintain a pseudodiaxial arrangement of the C2' and C3' vicinal fluorine atoms. These data, along with previously reported data by us and others concerning monofluorinated nucleoside conformations, were used to propose a model of how fluorine influences different aspects of nucleoside conformations.     

Semiquantitative determination of aromatic andα,β-unsaturated aldehydes by circular thin-layer chromatography

Summary A method for semiquantitative determination of aromatic and,-unsaturated aldehydes such as salicylaldehyde, anisaldehyde, vanillin, veratraldehyde, piperonal, cinnamaldehyde, furfural andp-dimethylaminobenzaldehyde by making circular spots of their isonicotinoyl hydrazones on chromatoplates with circular thin-layer Chromatographic apparatus and their comparison with sensitivity standards has been described. The accuracy is ± 5% and the method is rapid, simple and economical.

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Zusammenfassung Ein Verfahren zur semiquantitativen Bestimmung aromatischer und,-ungesättigter Aldehyde wie Salioylaldehyd, Anisaldehyd, Vanillin, Veratrumaldehyd, Piperonal, Zimtaldehyd, Furfural und p-Dimethylaminobenzaldehyd durch Dünnschicht-Ringchromatographie ihrer Isonikotinsäurehydrazone und Vergleich mit Standardchromatogrammen wurde beschrieben. Die Genauigkeit beträgt ±5%.

     

Circular thin-layer chromatography of aromatic andα,β-unsaturated aldehydes

Summary A simple method based on circular thin-layer chromatography is described for the separation of aromatic and,-unsaturated aldehydes as their isonicotinoyl hydrazones. The development of the chromatoplate is complete within 2 minutes.

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Zusammenfassung Aromatische und,-ungesättigte Aldehyde lassen sich durch ringförmige Dünnschichtchromatographie ihrer Isonikotinoylhydrazone trennen. Die Entwicklung der Dünnschichtplatten ist innerhalb 2 Minuten zu bewerkstelligen.

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Résumé On décrit une méthode simple fondée sur la chromatographie circulaire en couche mince pour séparer les aldéhydes aromatiques et, non saturés, sous forme de leurs hydrazones isonicotinoyles. Le développement de la chromatoplaque est complet en deux minutes.

     

Direct Formic Acid Mediated Z‐Selective Reductive Coupling of Dienes and Aldehydes

Methods for the addition of unsaturated nucleophiles to carbonyls to generate Z‐olefin products remain rare and often require either alkyl borane or zinc reductants, limiting their utility. Demonstrated here is that formic acid mediates the Rh‐catalyzed, Z‐selective coupling of dienes and aldehydes. The process is distinguished by broad tolerance towards reducible or electrophilic groups. Kinetic analysis suggests that generation of the catalytically active Rh intermediate by ligand dissociation is the rate‐determining step. The rapid generation and trapping of Rh‐allyl intermediates is key to preventing chain‐walking isomerization events that plague related protocols. Insights gained through this study may have wider implications in selective metal‐catalyzed hydrofunctionalization reactions.