Biological Investigation of Amaryllidaceae Alkaloid Extracts from the Bulbs of Pancratium trianthum Collected in the Senegalese Flora

Amaryllidaceae plants are rich in alkaloids with biological properties. Pancratium trianthum is an Amaryllidaceae species widely used in African folk medicine to treat several diseases such as central nervous system disorders, tumors, and microbial infections, and it is used to heal wounds. The current investigation explored the biological properties of alkaloid extracts from bulbs of P. trianthum collected in the Senegalese flora. Alkaloid extracts were analyzed and identified by chromatography and mass spectrometry. Alkaloid extracts from P. trianthum displayed pleiotropic biological properties. Cytotoxic activity of the extracts was determined on hepatocarcinoma Huh7 cells and on acute monocytic leukemia THP-1 cells, while agar diffusion and microdilution assays were used to evaluate antibacterial activity. Antiviral activity was measured by infection of extract-treated cells with dengue virus (DENV_GFP) and human immunodeficiency virus-1 (HIV-1_GFP) reporter vectors. Cytotoxicity and viral inhibition were the most striking of P. trianthum’s extract activities. Importantly, non-cytotoxic concentrations were highly effective in completely preventing DENV_GFP replication and in reducing pseudotyped HIV-1_GFP infection levels. Our results show that P. trianthum is a rich source of molecules for the potential discovery of new treatments against various diseases. Herein, we provide scientific evidence to rationalize the traditional uses of P. trianthum for wound treatment as an anti-dermatosis and antiseptic agent.     

Correction to: Densities of Active Species in R/x%(N2–5%H2) (R = Ar or He) Microwave Flowing Afterglows

Plasma Chemistry and Plasma Processing - Unfortunately, the original publication contains errors. The authors would like to correct the errors as given.     

Universal computation in fluid neural networks

Fluid neural networks can be used as a theoretical framework for a wide range of complex systems as social insects. In this article we show that collective logical gates can be built in such a way that complex computation can be possible by means of the interplay between local interactions and the collective creation of a global field. This is exemplified by a NOR gate. Some general implications for ant societies are outlined. © 1996 John Wiley & Sons, Inc.     

Stereochemistry and some synthetic uses of the heteroarylation of phospholes

Further studies have been conducted on the condensation of electron-rich arenes or heteroarenes with the dienic system of phosphole P-complexes. According to the X-ray crystal structure analysis of one of the resulting 2-aryl-3-phospholene P-complexes, the condensation takes place on the side of the diene opposite to the complexing group. The decomplexation of the phospholene P–Mo(CO)₅ and P–W(CO)₅ complexes, respectively, by reaction with sulfur or halogens and tertiary amines yields the corresponding P-sulfides and oxides with full retention of the stereochemistry at phosphorus. Double condensation of the phosphole P-complexes onto the 2 and 5 positions of thiophene and furan ultimately leads to phosphole–thiophene–phosphole and phosphole–furan–phosphole chains. The first type has been characterized by X-ray crystal structure analysis of its P,P-disulfide. No electronic delocalization appears to take place along the chain.     

Degradation of Fatty Acid Phase-Change Materials (PCM): New Approach for Its Characterization

The use of adequate thermal energy storage (TES) systems is an efficient way to achieve thermal comfort in buildings reducing the cooling and heating demand. Besides, deploy phase change materials (PCM) to meet and enhance the TES needs is highly effective and widely studied. In this paper, a study of the degradation of two fatty acids is presented, capric and myristic acids, in order to evaluate whether their thermo-physical properties are affected throughout time during service. This was carried out by means of two different types of thermal treatments: degradation at constant temperature (thermal stability test), 60 °C during 100 h and 500 h, and degradation with heating and cooling cycling (thermal cycling stability), between a temperature range from 15 °C to 70 °C with 0.5 °C/min ramp during 500 and 1000 cycles. Despite no significant changes were measured for myristic acid, experimental results revealed a decrease of melting enthalpy of 6.6% in capric acid thermally treated for 500 h. Evidences of chemical degradation were found that might explain the decrease in thermophysical properties during use.     

Dynamics of the Water–Oil Front for Two-Phase, Immiscible Flow in Heterogeneous Porous Media. 1 – Stratified Media

We study the evolution of the water–oil front for two-phase, immiscible flow in heterogeneous porous media. Our analysis takes into account the viscous coupling between the pressure field and the saturation map. Although most of previously published stochastic homogenization approaches for upscaling two-phase flow in heterogeneous porous media neglect this viscous coupling, we show that it plays a crucial role on the dynamics of the front. In particular, when the mobility ratio is favorable, the viscous coupling induces a transverse flux that stabilizes the water–oil front, which follows a stationary behavior, at least in a statistical sense. Calculations are based on a double perturbation expansion of equations at first order: the local velocity fluctuation is defined as the sum of a viscous term related to perturbations of the saturation map, on one hand, plus the perturbation induced by the heterogeneity of the permeability field with a base-state saturation map, on the other hand. In this first paper, we focus on flows in stratified reservoirs, with stratification parallel to the mean flow. Our results allow to predict the evolution of large Fourier mode of the front, and the emergence of a stationary front, for favorable mobility ratios. Numerical experiments confirm our predictions. Our approach is applied to downscaling. Extension of our theory to isotropic media is presented in the companion paper.     

Stereoselective Aminoxylation of Biradical Titanium Enolates with TEMPO

A highly efficient and straightforward aminoxylation of titanium(IV) enolates from (S)‐N‐acyl‐4‐benzyl‐5,5‐dimethyl‐1,3‐oxazolidin‐2‐ones with TEMPO has been developed. A wide array of functional groups on the acyl moiety, including alkyl and aryl substituents, olefins, esters, or α‐cyclopropyl, as well as α‐trifluoromethyl groups, are well tolerated. This transformation can therefore produce the α‐aminoxylated adducts in excellent yields with high diastereomeric ratios (d.r.). In turn, parallel additions to the α,β‐unsaturated N‐acyl counterparts give the corresponding γ‐adducts with complete regioselectivity in moderate to good yields. Removal of the piperidinyl moiety or the chiral auxiliary converts the resultant adducts into enantiomerically pure α‐hydroxy carboxyl derivatives, alcohols, or esters in high yields under mild conditions. Finally, a new mechanistic model based on the biradical character of the titanium(IV) enolates has been proposed.