Future Shorelines: A Living Shoreline Site Selection and Design Decision Support Tool that Incorporates Future Conditions Induced by Sea Level Rise.

Most living shoreline site selection and design decision support tools are based upon existing environmental conditions. We developed a web-based, geospatial tool called Future Shorelines that integrates high-resolution landscape elevation data and a matrix of locally derived NOAA Interagency Sea Level Rise Scenarios to characterize future conditions of submergence and shoreline translation induced by sea level rise. Once the practitioner selects a location of interest, sea level rise scenario (e.

Carnosic Acid Inhibits Herpes Simplex Virus Replication by Suppressing Cellular ATP Synthesis.

Acquiring resistance against antiviral drugs is a significant problem in antimicrobial therapy. In order to identify novel antiviral compounds, the antiviral activity of eight plants indigenous to the southern region of Hungary against herpes simplex virus-2 (HSV-2) was investigated. The plant extracts and the plant compound carnosic acid were tested for their effectiveness on both the extracellular and intracellular forms of HSV-2 on Vero and HeLa cells.

Synthesis, In Silico and Kinetics Evaluation of -(β-d-glucopyranosyl)-2-arylimidazole-4(5)-carboxamides and -(β-d-glucopyranosyl)-4(5)-arylimidazole-2-carboxamides as Glycogen Phosphorylase Inhibitors.

Recently studied -(β-d-glucopyranosyl)-3-aryl-1,2,4-triazole-5-carboxamides have proven to be low micromolar inhibitors of glycogen phosphorylase (GP), a validated target for the treatment of type 2 . Since in other settings, the bioisosteric replacement of the 1,2,4-triazole moiety with imidazole resulted in significantly more efficient GP inhibitors, in silico calculations using Glide molecular docking along with unbound state DFT calculations were performed on -(β-d-glucopyranosyl)-arylimidazole-carboxamides, revealing their potential for strong GP inhibition. The syntheses of the target compounds involved the formation of an amide bond between per--acetylated β-d-glucopyranosylamine and the corresponding arylimidazole-carboxylic acids.

Microcirculation-driven mitochondrion dysfunction during the progression of experimental sepsis.

Sepsis is accompanied by a less-known mismatch between hemodynamics and mitochondrial respiration. We aimed to characterize the relationship and time dependency of microcirculatory and mitochondrial functions in a rodent model of intraabdominal sepsis. Fecal peritonitis was induced in rats, and multi-organ failure (MOF) was evaluated 12, 16, 20, 24 or 28 h later (n = 8/group, each) using rat-specific organ failure assessment (ROFA) scores.