Antimicrobial activity of newly synthesized thienoquinolizidines derivatives: inspired by natural plant alkaloids

The antimicrobial activity of 16 newly prepared quinolizidines derivatives using bacteria (Staphylococcus aureus, Staphylococcus epidermidis, Proteus sp., Escherichia coli) acid fast bacterium Mycobacterium smegmatis, yeasts (Candida albicans, Candida parapsilosis), and filamentous fungi (Fusarium culmorum, Microsporum gypseum, Aspergillus flavus, Botrytis cinerea, Alternaria alternata) was studied in this paper. The best antibacterial properties were demonstrated by derivatives 11Ba, trans10Bb and 11Bb, and the most sensitive microorganism was found to be the gram-positive bacterium S. epidermidis. The derivative 11Bb showed the best antifungal activity, while C. albicans was resistant to all tested derivatives, and C. parapsilosis was fully inhibited in the presence of the derivative 11Ba and 11Bb. Among the filamentous fungi, only the dermatophyte M. gypseum was partially inhibited. Biofilms represent the most prevalent type of microbial growth in nature and are crucial to the development of clinical infections. Newly synthesized derivatives were also added into the medium throughout the biofilm formation. We have observed a significant decrease of biofilm formation in the presence of quinolizidine derivatives, testifying to their significant antimicrobial activity. It seems that the relationship between antimicrobial activity and the structure is based on the alkaline character due to nitrogen, the saturated basic quinolizidine skeleton, and the position of sulfur in the molecule.     

Necessarily Incompatible Consistent Wants

This paper argues that the wants or desires of a person can be consistent with each other and still necessarily incompatible with each other and for interesting reasons. It is argued here that this problem is not rare and that there is no solution in sight.     

Synthesis of heterocycles from arylacetonitriles: Powerful tools for medicinal chemists

Arylacetonitriles are versatile building blocks for the construction of heterocyclic scaffolds in medicinal chemistry. These intermediates are able to engage in a variety of synthetic transformations, giving rise to diverse biologically active structures. This digest focuses on recent applications of this synthetic methodology by drug discovery teams across several disease areas, with an emphasis on different reaction types.     

Ionization Constants of DL-2-Aminobutyric Acid and DL-Norvaline Under Hydrothermal Conditions by UV–Visible Spectroscopy

The first and second ionization constants for the amino acids DL-2-aminobutyric acid (DL-2-aminobutanoic acid) and DL-norvaline (DL-2-aminopentanoic acid) were determined under hydrothermal conditions, from 175 to 275 °C at 10 MPa, using thermally-stable colorimetric pH indicators (acridine, 4-nitrophenol and 2-naphthoic acid). The measurements were carried out by UV–visible spectroscopy using a high-temperature, high-pressure platinum flow cell with sapphire windows, which minimized the effects of thermal decomposition. The results were combined with literature values from titration calorimetry at 25–130 °C to yield an extended van’t Hoff model for the temperature dependence of the ionization constants for the carboxylic acid and ammonium groups, \( K_{\text{a,COOH}} \) and \( K_{{{\text{a,NH}}_{3}^{ + } }} \), over the entire temperature range. The experimental results for the second ionization constant \( K_{{{\text{a,NH}}_{3}^{ + } }} \) at elevated temperatures are consistent with the predictions from the Yezdimer–Sedlbauer–Wood functional group additivity model, but for the first ionization constant \( K_{\text{a,COOH}} \) are not. This suggests that the group contribution parameters for the standard partial molar heat capacity of the carboxylic acid group are in error, or that nearest neighbor interactions between the –COOH and \( - {\text{NH}}_{3}^{ + } \) groups cause a breakdown in the functional group additivity relationship.     

Calculating approximation guarantees for partial set cover of pairs

As a part of a heuristic for the fast detection of new word combinations in text streams, we consider the NP-hard Partial Set Cover of Pairs problem. There we wish to cover a maximum number of pairs of elements by a prescribed number of sets from a given set family. While the approximation ratio of the greedy algorithm for the classic Partial Set Cover problem is completely understood, the same question for covering of pairs is intrinsically more complicated, since the pairs insert some graph-theoretic structure. The best approximation guarantee for the first greedy step can be rephrased as a problem in extremal combinatorics: Assume that we may place a fixed number of subsets of fixed and equal size in a set, how many different pairs of elements can we cover? In this paper we introduce a method to calculate optimal approximation guarantees, and we demonstrate its use on the smallest set families.     

Determination of the thermal modification degree of beech wood using thermogravimetry

Thermal modification is one of the environmental friendly wood preservation technologies. During this process, changes of the main woody cell wall components occur, which lead to improved dimensional stability, lower hygroscopicity and improvement in biological durability. Several chemical reactions which occur during thermal treatment of wood caused changes in wood properties. During TG measurements, thermal decomposition reactions, which was not completed during previous thermal modification process, continued in wood samples, meaning that more thermally treated samples exhibited lower mass losses in a certain or whole temperature range up to 600 °C. Therefore, mass loss, obtained within selected temperature range, could be used as a marker of previous thermal treatment. The aim of the present work is to evaluate suitability of a thermogravimetric method (TG) for determination of a degree of thermal treatment of beech wood. On the basis of thermally untreated sample and those which were thermally modified at 180, 190, 200, 210, 215 and 220 °C in the absence of oxygen, respectively, and with known values of mass loss during the modification processes, several calibration curves were constructed. They represent mass loss in a certain temperature range during TG measurement versus mass loss during previous thermal modification. In a temperature range from 130 to 300 °C and from 130 to 320 °C under nitrogen atmosphere, a linear dependence was observed; correlation coefficients R ² were 0.87 and 0.91, respectively. In wider temperature range and under air atmosphere, lower correlation coefficients were obtained. High correlation coefficient, higher than 0.95, was observed in a temperature range from 25 to 130 °C under both atmospheres. In this region, dehydration due to rehydration of thermally modified samples occurs. The results of this work were compared with those obtained for Norway spruce.     

Zur Theorie der Rheopexie

Zusammenfassung Unter der Annahme, da\ die makromolekularen oder kolloiden Teilchen eines Systems durch die Einwirkung einer Scherung in einen Zustand überführt werden, in welchem sie zur Aggregatbildung befÄhigt sind, und dieser Proze\ sowie die Aggregation zu Flie\gleichgewichten führt, wird ein Reibungsgesetz abgeleitet, das auch das Flie\verhalten rheopexer Systeme wiederzugeben vermag. Es wird gezeigt, da\ mit Hilfe der erhaltenen Gleichung das verwickelte Flie\verhalten der Schmelze eines Epoxydharzes molekular-physikalisch verstanden werden kann.