Anhydrous Sodium Acetate Research Articles

Reaction of aroylpyruvic acids methyl esters with 4-aminobenzoic acid. Antioxidant activity of the obtained compounds

4-{[(2Z)-4-Aryl-2-hydroxy-4-oxobut-2-enoyl]amino}benzoic acids were synthesized by reacting methyl esters of aroylpyruvic acids with 4-aminobenzoic (p-aminobenzoic) acid in glacial acetic acid in the presence of anhydrous sodium acetate. 4-{[(2Z)-4-Aryl-1-methoxy-1,4-dioxobut-2-en-2-yl)]amino}benzoic acids were synthesized by reacting the above reagents in a mixture of glacial acetic acid–ethanol (1:1) without adding anhydrous sodium acetate. Structure of the obtained compounds was confirmed by 1H and 13C{1H} NMR and IR spectroscopy. The antioxidant activity of the synthesized compounds was studied.

Synthesis and Characterization of some new heterocyclic derivatives from aromatic carbonyl ‎compounds and carboxylic acids with Evaluation some of them for biological activity

In this research investigation, a total of eighteen diverse tetra- and penta-lateral cyclic compounds were synthesized. These included 1,3,4-thiadiazole, thiazolidin-4-one (via an alternative method), 1,2,4-triazole, carbothioamide, thiazole-4-one, azetidin-2-one, and oxazole. The synthesis procedure entailed a sequence of reactions. The thiazolidine-4-one 1 was obtained by reaction p-aminobenzoic acid with thiosemicarbazide, followed by treatment with p-tolualdehyde to produce Schiff base 2. Reaction Schiff base 2 with mercaptoacetic acid in dry benzene was carried out to produce thiazolidine-4-one 3. In another synthesis pathway, the esterification of p-nitro benzoic acid with ethanol in the presence of sulfuric acid was obtained to formation of compound 4. Compound 4 was subsequently reacted with thiosemicarbazide, yielding compound 5. Cyclization of compound 5 was then achieved using 4% sodium hydroxide solution. This formed the 1,2,4-triazole heterocycle, designated compound 6. Thiosemicarbazone 7-9 were prepared by reaction of thiosemicarbazide with different aldehydes. Additionally, 2-substituted-1,3-thiazolidine-4-one derivatives 10-12 were synthesized through the reaction of thiosemicarbazone with chloroacetic acid in the presence of anhydrous sodium acetate. The Oxazole derivative 15 was obtained through a series of reactions starting with the reaction of p-amino benzoic acid with ethyl chloroacetate, resulting in compound 13. Compound 13 was then treated with urea to obtain compound 14, followed by a reaction with 4-phenyl phenacyl bromide to yield the final product, the Oxazole derivative 15. The 2-aminooxadiazole derivative 16 was synthesized by reaction urea with 4-bromoacetophenone which was reacted with 4-bromobenzaldehyde to produce Schiff base derivative 17. Finally, β-lactam 18 is obtained through reaction Schiff base with chloroacetyl chloride in the presence of triethyl amine. FT-IR, 1H-NMR, and 13C-NMR spectroscopy were used to confirm their proposed structures. Moreover, the antibacterial and antifungal activities of certain synthesized compounds, specifically 2,3,6,11,13,15,17, and 18, were assessed against Staphylococcus aureus, Escherichia coli, and Candida albicans, demonstrating encouraging outcomes.Keywords: Antibacterial, antifungal activity, oxadaizole, heterocyclic derivatives, Oxazole.

Synthesis of New Glycosylamine Derivatives based on Carbohydrates

Background: Glycosylamine play an important role in living organisms. Most plants store their chemical resources in the form of inactive glycosides, which are broken down and con-verted into sugar in the body of herbivores by hydrolyzing enzymes. Glycosylamine are obtained from the secondary metabolism of plants and consist of two parts. One part of it contains sugar like glucose and is inactive in most substances, and has a good effect on the solubility of the glycosyla-mine derivatives and its absorption and even its transfer from one organ to another. The therapeutic effect is related to the second part, which is called aglycan (or aglucan). Glycosylamine derivatives form a large group of valuable medicinal substances, which at the same time include some of the most dangerous and toxic substances in nature. These substances are present in many groups of flowering plants. Glycosides are made in different ways in different metabolic pathways. These materials have a complex and special chemical structure and leave special effects on the human body. Glycosylamine derivatives are called O-glycosid, N-glycosid, S-glycosid in terms of atoms coupling to anomeric carbon. Carbohydrate esterification reaction to prepare new glycosylamine derivatives is one of the most important carbohydrate reactions. The anomeric position of carbohy-drates with strong leaving groups is very important for the preparation of glycosides. Preparation of glycosylamine derivatives based on acetylated carbohydrates is the main purpose of this article. Dif-ferent carbohydrates were acetylated under mild conditions and high yields. The anomeric position was deacetylated by a magnesium oxide heterogeneous catalyst in methanol solvent. In order to pre-pare new glycosides acetylated/ deacytylated carbohydrate reacted with N-Methyl-(naphtha-2-ylmethoxy)amine. The final product was identified by various spectroscopic methods. Methods: Anhydrous sodium acetate (4 g) and α-D-glucose (28 mg, 5 g) were mixed. The mixture was transferred to a 200 ml Round-bottom flask . Acetic acid (260 mg, 25 ml) was added to the reaction mixture. The reaction mixture was heated in a boiling water bath for 2 h until complete dissolution of the glucose. Then 100 ml of ice was added. After 1 hour, White crystals formed and were washed with cold water. And then 1 mol of glucose pentaacetate per 50 ml of methanol was dissolved by a magnetic stirrer. After thatMgO (0.2gr) was added to the reaction mixture. The re-action mixture was refluxed at room temperature within 4-5 hours. After 5 hours, the solvent was removed and separated by chromatography. It is then washed with hexane and crystallized by ether-hexane. And the final step reacted with N-Methyl- (naphtha-2-ylmethoxy) amine in order to prepare new glycosylamine derivatives. Results: Magnesium oxide in methanol solvent is one of the best effective catalysts in the deacetyla-tion of the anomer position of acetylated carbohydrates. It is done under ambient temperature and in very easy conditions and makes carbohydrates susceptible to extensive chemical reactions. One of these reactions is the formation of glycosides. Various carbohydrates are acetylated by acetic anhy-dride in the presence of sodium acetate, and the anomeric position is deacetylated by a heterogeneous catalyst. In order to prepare N-glycoside, the glycosides are reacted with N-alkoxy N-methylglycosyl amine. The final products are identified by various spectroscopic methods. Conclusion: Glucose, mannose, for example, were acetylated by acetic anhydride in the presence of sodium acetate. And the anomeric position of pentaacetate glucose was selectively deacetylated with magnesium oxide in a methanol solvent. Then, the reaction for the preparation of glycosylamine de-rivatives was carried out under very mild and easy conditions. The aminoglycosides synthesized in this article are used as raw materials for the synthesis of a wide range of antibacterials.

The role of cavitation and gas bubbles in the non-photochemical laser-induced nucleation of sodium acetate

Laser pulse nucleates anhydrous sodium acetate and stable gas bubbles from solution.

Interaction of DGAT1 polymorphism, parity, and acetate supplementation on feeding behavior, milk synthesis, and plasma metabolites

Acetate supplementation increases milk fat production, but interactions with animal-related factors have not been investigated. The objective of this study was to characterize the interaction of acetate supplementation with parity and genetic potential for milk fat synthesis including the DGAT1 K232A polymorphism (AA and KA genotypes). In total, 47 primiparous and 49 multiparous lactating cows were used in 2 blocks in a crossover design. The basal diet was formulated to have a low risk of biohydrogenation-induced milk fat depression and had 32.8% and 32.0% neutral detergent fiber and 21.7% and 23.6% starch [all on a dry matter (DM) basis] in block 1 and 2, respectively. The control treatment received the basal diet, and the acetate supplementation treatment included anhydrous sodium acetate supplemented to the basal diet at 3.2% and 3.1% of DM of the diet for block 1 and 2, respectively (targeting 10 mol/d of acetate). The DGAT1 genotype frequency of the experimental cows was 45% AA and 51% KA, with 4% cows with either a KK or unimputable genotype. Acetate supplementation increased DM intake (DMI) in KA multiparous cows, but acetate did not change DMI in AA multiparous or primiparous cows of either genotype. Acetate supplementation increased the frequency of meals by 8% and decreased the length of each meal by ∼5 min compared with control. There was no effect of acetate on milk yield. Acetate supplementation increased milk fat yield and concentration by 117 g/d and 0.31 percentage units, respectively, regardless of DGAT1 polymorphism or parity. The increase in milk fat yield was mostly due to an increase in yield of 16C mixed-sourced fatty acids, suggesting that acetate supplementation drives mammary de novo synthesis toward completion. Response to acetate supplementation was not related to genomic predicted transmitting ability of milk fat concentration and yield or to pretrial milk fat percent and yield, suggesting that acetate increases milk fat production regardless of genetic potential for milk fat yield and level of milk fat synthesis. Interestingly, analyzing the temporal effect on the interaction between treatment and DGAT1 polymorphism on milk fat yield suggested that DGAT1 polymorphism may affect the short-term response to acetate supplementation during the first ≤7 d on treatment. Acetate supplementation also increased plasma β-hydroxybutyrate concentration and decreased plasma glucose concentration. In conclusion, acetate supplementation consistently increased milk fat synthesis regardless of parity or genetic potential for milk fat synthesis.

An environmentally benign protocol for the synthesis of sugar 1,2-orthoesters in poly(ethylene glycol) dimethyl ether (DMPE)

An environmentally benign procedure has been developed for the synthesis of sugar orthoesters using anhydrous sodium acetate in poly (ethylene glycol)dimethyl ether (DMPE). Various sugar orthoesers were prepared without using volatile organic solvent and quaternary ammonium salt. The sugar orthoesters were obtained in good to excellent yields.

Regioselective three-component synthesis and theoretical calculations of new alkane-linked bis(thiazol-2(3H)-imine) hybrids: a DFT-based FMO and local reactivity indices

A three-component approach was conducted to adeptly prepare a new series of (Z)-bis(N-phenylthiazol-2(3H)-imines. The newly synthesized compounds were prepared by refluxing a ternary mixture of phenyl isothiocyanate, the suitable α-bromoketones, and alkane-linked diamines in ethanol. Reaction conditions were optimized by comparing the yield of the final product under various bases, solvents, temperatures, and base-to-starting-materials molar ratios. The intended hybrids were produced with 85–96% yields while using ethanol at 80 °C for 3–5 h in the presence of anhydrous sodium acetate. The ascribed configuration of new products as well as the regioselectivity of the one-pot reaction were confirmed using both spectral data (1D and 2D NMR) and DFT-calculation techniques.Graphical abstract

Synthesis and biological activity of 4-aryl-2-hydroxy-4-oxo-<i>N</i>-(2-sulfamoylphenyl)but-2-enamides

The reaction of methyl esters of 4-aryl-2-hydroxy-4-oxobut-2-enoic (aroylpyruvic) acids with 2-aminobenzenesulfonamide in glacial acetic acid in the presence of anhydrous sodium acetate, 4-aryl-2-hydroxy-4-oxo N -(2-sulfamoylphenyl)but-2-enamides were obtained. The analgesic and antimicrobial activity of the obtained compounds was studied.

Certified Reference Materials for Phase Transition Temperatures of Organic Substances On the Basis of Anhydrous Sodium Acetate and Sodium Methansulfonate

The requirements for thermal analysis instruments are increasing in terms of increasing the measurement ranges and improving their accuracy due to the development of scientific and technological progress in the field of metrological supervision, chemical and pharmaceutical industries. The study of determining the melting point of organic substances is of particular relevance for the metrological support of the applied thermal analysis instruments and traceability to the base units of physical quantities.The purpose of the research was to test the possibility of using organic substances on the basis of sodium acetate and sodium methanesulfonate as phase transition temperatures standards for candidate material to certified reference materials for phase transition temperatures (CRMs) traceable to the SI unit of the «temperature» value.The procedure for measuring the phase transition temperatures (melting point) was performed by differential scanning calorimetry using an STA 449 F5 JUPITER thermal analyzer from the GET 173–2017 State Primary Standard. The determination of the CRM certified value was performed in accordance with GOST ISO Guide 35–2015, the contributions to the uncertainty from the heterogeneity of the starting materials were evaluated, and the short-term and long-term stability of the materials were studied.The obtained metrological characteristics of the investigated batch of CRMs are as follows: the range of permissible certified characteristics of the melting point of the phase transition for anhydrous sodium acetate (328.35–330.35) °C, for sodium methanesulfonate (352.05–354.05) °C. Comparison of the certified melting point values of the developed CRMs with the reference melting point values presented in IUPAC showed that the certified characteristics of the CRMs are consistent within ±1.4 °C.The theoretical significance of the obtained results lies in the proof of the possibility of applying the method of differential scanning calorimetry for the development of certified reference materials for phase transition temperatures (a set of TPKR CRMs) GSO 11928–2022/GSO 11929–2022.The practical significance of the results obtained makes it possible to expand the possibility of establishing and controlling the calibration dependence of thermal analysis measuring instruments; certification of measurement procedures (methods) and accuracy control of the measurement results of the phase transition temperatures of metals, metal salts, metal oxides, polymeric materials, organic and inorganic substances.

Residue analysis of selected organophosphorus and organochlorine pesticides in commercial tomato fruits by gas chromatography mass spectrometry

In this study, analysis of some selected organophosphorus and organochlorine pesticides was carried out in tomato samples collected from the markets of Mettu town, Ilu Aba Bora Zone, Oromia, Ethiopia. The quick, Easy, Cheap, Effective, Rugged, and Safe (QuEChERS) method was used for the extraction of collected samples using acetonitrile with 1% acetic acid, anhydrous magnesium sulfate, and anhydrous sodium acetate, followed by dispersive solid-phase extraction (d-SPE). Chromatographic separation and quantitative determination of the pesticides were performed by gas chromatography equipped with a mass spectrometer. The calibration curves for each analyte constructed in tomato samples were linear in the concentration range of 2–200 μg/kg with R2 > 0.99 and the LODs and LOQs of the method were in the range of 0.01–0.04 μg/kg and 0.04–0.13 μg/kg, respectively. The recovery and precision study results were within acceptable standard guidelines. Of the fourteen pesticides tested, chlordane, hexachlorobenzene, 4, 4'-DDE, 4, 4'-DDD, 4, 4'- DDT, and profenofos were detected at 0.15, 0.09, 0.17, 0.032, 1.24 and 0.062 μg/kg, respectively. Despite the concentrations of the detected pesticides being lower than the maximum residue limit recommended by FAO/WHO, the presence of these toxic chemicals in tomatoes indicates product contamination and requires extensive further investigation with the inclusion of other pesticides.

Synthesis and Characterization of some New Amic acid and Imides and study the Biological Activity

This study includs the synthesis of some new Amic acid and Imides,starting from the esters [S1] of Terephthalic acid which then converted toits hydrazide [S2] then to amic acid derivatives [S3-S7] and finally withimides [S8-S12]. Preparing of ester [S1] by usual esterification ofterephthalic acid with absolute ethanol in acidic medium, then hasconverted to its hydrazide [S2] by reacting it with hydrazine hydrate. Theamic acid derivatives [S3-S7] have been synthesized by the reaction ofhydrazide [S2] with anhydrides (2,3-dimethyl malic anhydride, 3-nitrophthalic anhydride, hexahydro phthalic anhydride, Diphenic anhydride,tetra Phenyl phthalic anhydride) in diethyl ether. Imides [S8-S12] werealso synthesized by cyclization of amic acids derivatives using aceticacid anhydride and anhydrous sodium acetate. The synthesizedcompounds were identified by spectral methods UV, FT-IR and H1-NMR beside melting point and the purity was determined using (TLC)and some of its physical properties were measured. Some of thesecompounds were tested against four strains of bacteria (E. coli, P.ariginosa, S. aurous and S. pyogenes)

Optimization of medium composition of Lactobacillus plantarum Y44 using Plackett–Burman and Box–Behnken designs

The biomass of Lactobacillus strains depends on the culture media and culture conditions. The purpose of this study was to optimize the culture medium composition and culture conditions of Lactobacillus plantarum Y44 to improve its biomass. The utilization of different carbon sources and nitrogen sources by L. plantarum Y44 was assessed by single factor experiment to screen out the economical carbon and nitrogen sources for L. plantarum Y44 growth. Through optimization experiments, the optimized culture medium for L. plantarum Y44 growth consists of soybean peptone 44.1 g/L, yeast extract 22.1 g/L, sucrose 35.6 g/L, hydrogen diamine citrate 2 g/L, anhydrous sodium acetate 8.5 g/L, dipotassium hydrogen phosphate 4 g/L, Tween-80 2 mL/L, manganese sulfate 0.25 g/L, and magnesium sulfate 0.58 g/L, and the initial pH 6.7. The concentration of viable bacteria cells of L. plantarum Y44 culturing in the optimized medium at 37 °C for 16 h was up to 3.363 × 1010 CFU/mL, as 6.11 times higher than that in the MRS medium.

Interaction of sodium acetate supplementation and dietary fiber level on feeding behavior, digestibility, milk synthesis, and plasma metabolites.

Acetate supplementation has been shown to increase milk fat yield in diets with low risk of biohydrogenation-induced milk fat depression. The interaction of acetate supplementation with specific dietary factors that modify rumen fermentation and short-chain fatty acid (FA) synthesis has not been investigated. The objective of this experiment was to determine the effect of acetate supplemented as sodium acetate at 2 dietary fiber levels. Our hypothesis was that acetate would increase milk fat production more in animals fed the low-fiber diet. Twelve lactating multiparous Holstein cows were arranged in a 4 × 4 Latin square design balanced for carryover effects with a 2 × 2 factorial arrangement of dietary fiber level and acetate supplementation with 21-d experimental periods. The high-fiber diet had 32% neutral detergent fiber and 21.8% starch, and the low-fiber diet had 29.5% neutral detergent fiber and 28.7% starch created by substitution of forages predominantly for ground corn grain. Acetate was supplemented in the diet at an average 2.8% of dry matter (DM) to provide approximately 10 mol/d of acetate as anhydrous sodium acetate. Acetate supplementation increased DM intake by 6%, with no effect on meal frequency or size. Furthermore, acetate supplementation slightly increased total-tract apparent DM digestibility and tended to increase organic matter digestibility. Acetate supplementation increased milk fat concentration and yield by 8.6 and 10.5%, respectively, but there was no interaction with dietary fiber. The increase in milk fat synthesis was associated with 46 and 85 g/d increases in the yield of de novo (<16C) and mixed source (16C) FA, respectively, with no changes in yield of preformed FA (>16C). There was a 9% increase in the concentration of milk mixed-source FA and a 7% decrease in milk preformed FA with acetate supplementation, regardless of dietary fiber level. Acetate supplementation also increased the concentrations of plasma acetate and β-hydroxybutyrate, major metabolic substrates for mammary lipogenesis. Overall, acetate supplementation increased milk fat yield regardless of dietary fiber level through an increase mostly caused by an increase in longer-chain de novo FA, suggesting stimulation of mammary lipogenesis. The heightened mammary de novo lipogenesis was supported by an increase in the concentration of metabolic substrates in plasma.

Preparation of Iron Oxide Adsorbent Modified by Chitosan Biomaterials and Its Adoption in the Adsorption of Heavy Metals

Heavy metals in water leads to many ecological and environmental problems. All kinds of new magnetic adsorbents are used to adsorb the heavy metals in the aqueous solution, which has the advantages of high efficiency, low consumption, simplicity, convenience, and industrialization. Firstly, Fe3O4 is dissolved, and polyethylene glycol (PEG) and anhydrous sodium acetate are added. The dissolved product is placed in the reaction kettle lined with Teflon and reacts at a high temperature to obtain the Fe3O4 magnetic microspheres. The product is dissolved again. After the ultrasonic water bath, 1 mL tetraethyl orthosilicate (TEOS) is added drop by drop to obtain the SiO2/Fe3O4 magnetic microspheres by the ultrasonic and water-bath stirring. The magnetic microspheres are dissolved in 10 mL 3% chitosan solution. Chitosan/SiO2/Fe3O4 (CSF) magnetic adsorbent is obtained after ultrasonic agitation, and chitosan-biomodified iron oxide adsorbent (EDCSF) is obtained by the ethylene diamine tetraacetic acid (EDTA) modification. After the adsorbent is obtained, the biomaterial is characterized, and its performance of adsorbing heavy metals in water is tested as an adsorbent. In the experiment, the Fourier Transform Infrared Spectroscopy (FTIR) is used to verify that EDTA successfully modifies the surface of the CSF magnetic adsorbent. Through the morphology analysis and nitrogen adsorption–desorption test, EDTA cross-linked with the amino group of chitosan through carbodiimide can cause a decrease in the related physical indexes of the material. Thermogravimetric analysis (TGA) and hysteresis loop tests show that although the magnetism of CSF and EDCSF decreases, the solid–liquid separation is achieved in a relatively short time under the action of magnets. In the adsorption test, EDCSF shows an ideal adsorption performance for Cu(II), Cd(II), and Pb(II) in aqueous solution. With pH = 4.7 and at normal temperature, the maximum saturated adsorption capacity of EDCSF for Cu(II), Cd(II), and Pb(II) is 0.696 mmol/g, 0.586 mmol/g, and 0.562 mmol/g, respectively.

Solubility of Organic Salts in Solvent-Antisolvent Mixtures: A Combined Experimental and Molecular Dynamics Simulations Approach.

We combine molecular dynamics simulations with experiments to estimate solubilities of an organic salt in complex growth environments. We predict the solubility by simulations of the growth and dissolution of ions at the crystal surface kink sites at different solution concentrations. Thereby, the solubility is identified as the solution’s salt concentration, where the energy of the ion pair dissolved in solution equals the energy of the ion pair crystallized at the kink sites. The simulation methodology is demonstrated for the case of anhydrous sodium acetate crystallized from various solvent–antisolvent mixtures. To validate the predicted solubilities, we have measured the solubilities of sodium acetate in-house, using an experimental setup and measurement protocol that guarantees moisture-free conditions, which is key for a hygroscopic compound like sodium acetate. We observe excellent agreement between the experimental and the computationally evaluated solubilities for sodium acetate in different solvent–antisolvent mixtures. Given the agreement and the rich data the simulations produce, we can use them to complement experimental tasks, which in turn will reduce time and capital in the design of complicated industrial crystallization processes of organic salts.

Statistical Optimization of Novel Medium to Maximize the Yield of Exopolysaccharide From Lacticaseibacillus rhamnosus ZFM216 and Its Immunomodulatory Activity.

The traditional media used for the fermentation of Lactobacilli always contain carbohydrate polymers, which interfere with the analysis of the exopolysaccharide (EPS) produced by the bacteria. In this investigation, a novel medium formulation that could avoid such interference was successfully developed. The beef extract, yeast extract, and peptone used in this formulation were subjected to the removal of polysaccharides before use. The factors affecting the EPS production were optimized by a single factor test, Plackett–Burman design, and Box–Behnken design. The optimum formula was ascertained as: 7.5 g L–1 yeast extract, 12.5 g L–1 beef extract, 10 g L–1 peptone, 21.23 g L–1 maltose, 5.51 g L–1 yeast nitrogen base, 2 g L–1 K2HPO4, 5 g L–1 anhydrous sodium acetate, 2 g L–1 ammonium citrate, 0.58 g L–1 MgSO4⋅7H2O, 0.25 g L–1 MnSO4⋅H2O, and 1 mL L–1 Tween 80. The initial pH of the medium was 6.5. The optimized conditions for fermentation of the strain to produce EPS were as follows: seed size 1%, culture temperature 37°C, and culture time 20 h. Optimum results showed that EPS yield was 496.64 ± 3.15 mg L–1, being 76.70% higher than that of unoptimized conditions (281.07 ± 5.90 mg L–1). The EPS was mainly comprised of glucose and guluronic acid, with a weight average molecular weight of 19.9 kDa; it was also characterized by Fourier transform infrared spectroscopy and UV analysis. EPS was found to significantly enhance the phagocytic capacity, promote the NO, TNF-α, IL-1β, and IL-6 secretion, and improve mRNA expression of cytokines in RAW 264.7 macrophages, indicating its considerable immunomodulatory activity. Western bolt and immunofluorescence results demonstrated that the EPS was able to increase p65 nuclear translocation in the macrophages, indicating that EPS enhanced immunity via the NF-κB signaling pathway. EPS investigated in this work has potential as an attractive functional food supplement candidate for the hypoimmunity population.

One-Pot Synthesis of Novel Hydrazono-1,3-Thıazolıdın-4-One Derivatives as Anti-HIV and Anti-Tubercular Agents: Synthesıs, Bıologıcal Evaluatıon, Molecular Modelling and Admet Studıes

The necessity for newer anti-HIV and anti-tubercular medications has arisen as a result of the prevalence of opportunistic infections caused by HIV (human immunodeficiency virus). A series of ten new hydrazono 1,3-thiazolidin-4-one derivatives were synthesized in one-pot and evaluated for anti-HIV and anti-tubercular activities. Molecular Docking was accomplished with HIV-1 reverse transcriptase protein (PDB ID: 1REV) and Mycobacterium Tuberculosis (M. tuberculosis) H37Rv protein (PDB ID: 2YES) receptors along with drug-likeness and ADMET properties. One-pot synthesis of hydrazono 1,3-thiazolidin-4-one derivatives was carried out by ketones, thiosemicarbazide and ethylchloroacetate with the catalyst of anhydrous sodium acetate. All the synthesized compounds were characterized and evaluated for their in-vitro anti-HIV and also evaluated for their in-vitro anti-tubercular activity against M. tuberculosis H37Rv. In-silico predicted physicochemical parameters were done by MedChem DesignerTM software version 5.5 and ADMET parameters by pkCSM online tool. Furthermore, molecular docking was performed with pyrx 0.8 by autodock vina software. All the synthesized compounds were characterized and evaluated for their in-vitro anti- HIV activity for inhibition of syncytia formation, which shows KTE1 with EC50 47.95 μM and Selectivity Index (SI) of >4.17 and for inhibition of p24 antigen production EC50 was found to be 80.02 μM and SI of >2.49. The compounds were also evaluated for their in-vitro anti-tubercular activity against M. tuberculosis H37Rv, in which KTE1 MIC values of 12.5μg/ml with SI of >4.0 and cytotoxicity against Vero cell lines. In-silico predicted physicochemical parameters for synthesized compounds which were found to be drug-like. Furthermore, docking has shown a good dock score and binding energy with anti-HIV and anti-tubercular receptors. From the novel synthesized molecules, none of the molecule is as effective as standards for anti-HIV and anti-tubercular drugs and hence can be further explored for its potential activities. Furthermore, derivatization was made to achieve more potent compounds for anti-HIV and anti-tubercular drugs.

Effects of Replacing Dietary Fish Meal by Soybean Meal Co-Fermented Using Bacillus subtilis and Enterococcus faecium on Serum Antioxidant Indices and Gut Microbiota of Crucian Carp Carassius auratus

Fermented soybean meal (FSM) is an important feed material that can replace fish meal to solve the shortage of animal protein. To improve the utilization of FSM, we optimized the co-fermentation conditions of soybean meal using Bacillus subtilis and Enterococcus faecium and studied the effects of replacing fish meal with different proportions of FSM on serum antioxidant indices and gut microbiota (GM) composition of crucian carp (Carassius auratus). Our results showed that the co-fermentation of soybean meal was the most effective when the ratio of B. subtilis X-2 and E. faecium X-4 was 2:3, glucose addition was 4.5%, KH2PO4 addition was 0.15%, MgSO4·7H2O addition was 0.1%, anhydrous sodium acetate addition was 0.4%, fermentation time was 120 h, and the solid–water ratio was 1:1. Replacing 40% fish meal with FSM in the feed significantly improved the serum T-AOC, POD, and IgM levels in C. auratus. Although there were significant differences in the midgut and hindgut microbiota structures of C. auratus, the addition of FSM to the feed did not cause significant differences in the GM structure, whether in the midgut or hindgut. Therefore, 40% FSM is the most suitable substitute for fish meal in the feed of C. auratus.

Comarine derivatives designed as carbon dioxide and hydrogen storage

The growing of fossil fuel burning leads to increase CO2 and H2 emissions, which cause increasing of global warming that, has brought big attention. As a result, enormous researches have been made to reduce CO2 and H2 build up in the environment. One of the most promising approaches for managing CO2 and H2 gases percentage in the atmosphere is capturing and storage them inside proper materials. Therefore, the design of new materials for carbon dioxide and hydrogen storage has received increasing research attention. Four derivatives of coumarine linked to thiazolidinone were synthesized in good yields by reacting 3-(2-Phenylamino-acetyl)coumarine and 2-phenylimino thiazolidinone-4-one in a solution of anhydrous sodium acetate/ glacial acetic acid at 120° for 5–6 h. The synthesised organic compounds were identified by using different techniques such as 1H NMR, 13C NMR, FTIR, and energy dispersive X-ray spectra. The agglomeration, shape and porosity of the particles were determined utilizing scanning electron microscopy (SEM) and microscopy images analysis. The capacity of carbon dioxide (CO2) and hydrogen (H2) adsorption on the prepared organic materials at 323 K, 50 bar ranged from 22 to 31 cm3/g, and hydrogen from 4 to 12 cm3/g for the four synthesised compounds which contain phenyl substituted with chloro, nitro and bromo groups was found to be the most active adsorbent surfaces for carbon dioxide and hydrogen storage.

Synthesis of sodium acetate oriented Ni (II)-doped iron oxide nanospheres for efficient acetone sensing

Monodisperse pure and nickel-doped iron oxide NixFe3-xO4 (x ​= ​0.00, 0.02, 0.04, and 0.06) nanospheres were synthesized by hydrothermal method. The synthetic method was featured by using a structure directing agent, namely, anhydrous sodium acetate and ferric ions source, iron (III) chloride in an ethylene glycol solution without any kind of surfactant or template involved. The molar ratio of salts to anhydrous sodium acetate was optimized to 1:4 to get monodispersed and uniform spherical nanostructures. The sensing response of nickel doped iron oxide to different gases such as acetone, ammonia, sulphur dioxide, hydrogen sulphide, ethanol and methanol are accomplished at room temperature with the gas concentration of 5 ​ppm and was found selective towards acetone with response 29.9%. The response of NixFe3-xO4 (x ​= ​0.06) nanospheres were found to be 29.9%, 46%, 66%, 106%, and 174% towards 5, 10, 15, 20 and 25 ​ppm acetone concentration respectively. The response and recovery time at 5 ​ppm acetone concentration was found to be 94 ​s and 68 ​s respectively. Based on the reproducibility and stability test, it was observed that the fabricated sensor based on nickel doped iron oxide is highly reliable. The energy band diagram of the sensing mechanism of NixFe3-xO4 (x ​= ​0.06) nanospheres upon exposure to air and acetone atmosphere are presented.