A rhodamine-naphthalimide-benzamide trichromophoric system with solid-state and multiple solvent dependent aggregate emissive properties

A multiresponsive rhodamine-naphthalimide-benzamide conjugate was synthesised in high yield in three steps. The trichromophoric system formed emissive aggregates in pure DMSO that were remarkably sensitive to traces of water (<1...

Solubility Data and Computational Modeling of Baricitinib in Various (DMSO + Water) Mixtures

The solubility and thermodynamic analysis of baricitinib (BNB) in various dimethyl sulfoxide (DMSO) + water mixtures were performed. The “mole fraction solubilities (xe)” of BNB in DMSO and water mixtures were determined at “T = 298.2–323.2 K” and “p = 0.1 MPa” using an isothermal saturation technique. “Hansen solubility parameters (HSPs)” of BNB, pure DMSO, pure water and “DMSO + water” mixtures free of BNB were also estimated. The xe data of BNB was regressed well by five different thermodynamics-based co-solvency models, which included “Apelblat, Van’t Hoff, Yalkowsky-Roseman, Jouyban-Acree and Jouyban-Acree-Van’t Hoff models” with overall deviations of <5.0%. The highest and lowest xe value of BNB was computed in pure DMSO (1.69 × 10−1 at T = 323.2 K) and pure water (2.23 × 10−5 at T = 298.2 K), respectively. The HSP of BNB was found to be closer to that of pure DMSO. Based on activity coefficient data, maximum solute–solvent molecular interactions were observed in BNB-DMSO compared to BNB-water. The results of “apparent thermodynamic analysis” indicated endothermic and entropy-drive dissolution of BNB in all “DMSO + water” combinations including mono-solvents (water and DMSO). “Enthalpy-entropy compensation analysis” showed enthalpy-driven to be the main mechanism of solvation of BNB.

EFFECT OF CONCENTRATION AND NATURE OF LITHIUM SALT ON CHARACTERISTICS OF GEL ELECTROLYTES DMSO-PVDF-LiAn

The results of the study of electrolytes based on gel solutions of DMSO-PVDF-lithium salt with concentrations up to 0.05 m.f. and above 0.1 m.f. are presented. It is shown that the conductivity of electrolytes is close to the conductivity of lithium salt solutions in pure DMSO and obeys the Arrhenius equation in the studied range of temperatures and concentrations. The calculated activation energies for electrolytes with a salt concentration of up to 0.05 m.f. are 14–15.4 KJ/Mol, and for electrolytes with a salt concentration above 0.1 m.f. - 16.9–20.6 KJ/Mol indicate a fast ion transfer, which in more concentrated solutions is inhibited by an increase in their crystallinity. The analysis of the equivalent circuit models of the Li-Li systems electrochemical impedance spectra showed the tendency of electrolytes to form capacitive elements at the lithium electrode-electrolyte interface. It was recognized the presence of semi-infinite diffusion in LiClO4 and LiIm with salt concentration of 0.05 m.f., due to the imperfection of the film formed on the electrode surface. The efficiency of using DMSO-PVDF-lithium gel electrolytes on steel and platinum electrodes was analyzed by voltammograms.

PHYTOCHEMICAL INVESTIGATION AND PHARMACOLOGICAL ACTIVITIES OF HELIOTROPIUM CURASSAVICUM LINN

The current study was focused on the phytochemical investigation and pharmacological activities of the various fractions (methanolic crude, defatted methanolic, n-hexane, dichloromethane, ethylacetate and water) of H. curassavicum. The various plant extracts were examined for the total phenolic contents by taking Gallic acid as a standard, antioxidant scavenging assay by using DPPH (2, 2diphenyl-1-picrylhydrazy) & ABTS [2, 2-azinobis (3ethylbenzthiazoline-6-sulphonic acid)] free radicals, antifungal assay by using Terbinafine solution in DMSO as positive control and pure DMSO as negative control and in-vitro antibacterial activity. Methanolic crude extract showed high phenolic contents and significant antioxidant activity (both DPPH & ABTS). All other fractions were also found to have significant potential.

Novel N-(2-bromo-phenyl)-2-hydroxy-benzamide Derivatives with Antifugal Activity

In order to increase the biological activity, some novel molecules, esters, hydrazides, hydrazones of N-(2-bromo-phenyl)-2-hydroxy-benzamide, were obtained in good yields (86-93%), working at 150 �C, 500 W, 7-11 min, under microwave irradiation. All synthesized compounds were characterized using modern physico-chemical methods (FTIR, 1H-NMR, 13C-NMR and elemental analysis). Eight dilutions in dimethyl sulfoxide of these derivatives were tested against two phyto-pathogenic fungi, Fusarium oxysporum, Sclerotinia sclerotiorum and one common yeast, Saccharomyces cerevisiae. The antifungal activity was assessed using disc diffusion method, both negative, pure DMSO, and positive control, nystatin, were used. S. cerevisiae was slightly more sensitive than filamentous fungi, the strongest inhibition, MIC=0.3125g/L, was observed for N-(2-bromo-phenyl)-2-hydroxy-benzamide and N-(2-bromo-phenyl)-2-(4-dimethylamino-benzylidene-hydrazinocarbonylmethoxy)-benzamide. The most active compounds against F. oxysporum and S. sclerotiorum were N-(2-bromo-phenyl)-2-hydroxy-benzamide (MIC= 0.625g/L), N-(2-bromo-phenyl)-2-hydrazinocarbonylmethoxy-benzamide (MIC=1.25g/L) and N-(2-bromo-phenyl)-2-(4-dimethylamino-benzylidene-hydrazinocarbonyl-methoxy)-benzamide (MIC=0.625g/L), N-(2-bromo-phenyl)-2-hydrazinocarbonyl-methoxy-benzamide (MIC=1.25g/L), respectively.

Fractionation of DMSO-Extracted and NaOH-Extracted Hemicelluloses by Gradient Ethanol Precipitation from Neosinocalamus affinis

Neosinocalamus affinis hemicelluloses were extracted with pure DMSO and 3% NaOH in sequence. The DMSO- and NaOH-extracted hemicelluloses were then successively fractionated by gradient ethanol precipitation. NaOH-extracted hemicellulosic fractions with different branch degree could be separated by gradient ethanol precipitation, while DMSO-extracted hemicellulosic fractions could not. FT-IR spectra showed that DMSO-extracted fractions have more complete structure, while NaOH-extracted fractions have no acetyl at all. The FT-IR and NMR revealed that the DMSO-extracted Neosinocalamus affinis hemicelluloses were 4-O-methyl-glucuronoarabinoxylans consisting of a linear (1→4)-β-D-xylopyranosyl backbone with branches at O-2,3 of acetyl, O-2 of 4-O-methyl-a-D glucuronic acid, and O-3 of arabinose.

Oxaliplatin reacts with DMSO only in the presence of water

Oxaliplatin is stable in pure water and pure DMSO, but reacts rapidly in a mixture of the two solvents.