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A new fluorescent sensor 2-(2-(3-chloro-4-fluorophenyl)hydrazono)-5,5-dimethyl cyclohexane-1,3-dione (A) and 2-(2-(4-chloro-2-nitrophenyl)hydrazono)-5,5-dimethyl cyclohexane-1,3-dione (B) composed of a β-diketones of aryl hydrazones synthesized by simple and cost-effective method. Various analytical tools analyzed the structural investigations of the synthesized substituted β-diketones of aryl hydrazones like FT-IR, 1 H, 13 C NMR and UV-Vis techniques, Single-crystal X-ray diffraction studies (SCXRD) (for A), Scanning electron microscopy (SEM), and fluorescence spectroscopy. SEM also investigates surface morphology modifications of aryl hydrazones and Ni 2+ complex. Furthermore, the metal sensing (Chemo sensing) behavior of newly prepared aryl hydrazones of β-diketones derivatives was further studied by fluorescence spectroscopy. The aryl hydrazones sensor materials show admirable fluorescence selectivity with enrichment to Ni 2+ over different cations in an aqueous ethanol solution with a recognition extremity of 4 μM-7 μM. A joint experimental and theoretical investigation was led on the chemical structure employing a density functional theory (DFT) (B3LYP), engaging a 6-31G basis set. The DFT technique's enhanced geometrical bond angles and lengths exhibited great covenant with the experimental results. The highest occupied molecular (HOMO) orbital and lowest unoccupied (LUMO) molecular orbital energy has been concluded. The cytotoxicity studies show these compounds impede the growth of KB cells highly and from the studies to evaluate their capability to accurately dock aryl hydrazones to antibodies of cancer protein such as 4LRH, 4L9K, 4 EKD and 4GIW cancer proteins., (Copyright © 2022 Elsevier Ltd. All rights reserved.)

The photocatalytic performance of a semiconducting catalytic system is strongly influenced by charge-carrier separation rate, charge transport properties, surface area, utilization of light energy, and interface bonding. Herein, a series of bismuth vanadate (BiVO 4 ) samples were prepared via hydrothermal method by changing the volume ratios of ethelene glycol and ethanol as a solvent mixture for bismuth precursors. Further, the optimized BiVO 4 sheets with hierarchical morphology were used to construct an interface with rod-like g-C 3 N 4 materials, which was confirmed by HRSEM and HRTEM. Due to the formation of an effective interface bonding between BiVO 4 /g-C 3 N 4 , the photoinduced charge carrier's recombination rate was suppressed as confirmed by the PL analysis. The prepared BiVO 4 /g-C 3 N 4 sample were used to assess the photodegradation efficiency of Rhodamine B (RhB) under direct sunlight irradiation and the photocatalysts degraded ~92.8% of RhB within 2 h. The TOC measurements revealed a 66.4% mineralization efficiency for RhB. In addition, the radical trapping experiments demonstrated that superoxide and hydroxyl radicals are the main reactive species for the degradation. Based on the experimental evidences, a plausible charge transfer mechanism has been proposed. The enhanced photocatalytic activity has been mainly attributed to the inhibition of the recombination rate, enhanced charge carrier transfer efficiency, and high rate of production of reactive species., (Copyright © 2021 Elsevier Ltd. All rights reserved.)

A series of nitric oxide (NO) donor furoxan conjugates of N, N-dialkylcarboxy coumarins have been synthesized as potential anticancer agents. The synthesized compounds have been tested for their in vitro antiproliferative activities on various cancer and noncancerous cell lines. The candidate derivatives exhibit selectivity towards cancer cells with excellent activities in low nM to µM concentrations. In vitro mechanistic studies indicate that the candidate compounds generate substantial NO, inhibit colony formation, and cause apoptosis in cancer cells. A preliminary in vivo tolerance study of the lead candidate 10 in mice indicates that it is well-tolerated, evidenced by zero mortality and normal body weight gains in treated mice. Further translation of the lead derivative 10 using MDA-MB-231 based tumor xenograft model shows good tumor growth reduction., (Copyright © 2021 Elsevier Ltd. All rights reserved.)

Several phosphonium derivatives have been synthesized from Baylis-Hillman (BH) reaction derived allyl bromides and aryl phosphines as mitochondria targeting anticancer agents. In vitro cell proliferation inhibition studies on various solid tumor cell lines indicate that most of the compounds exhibit IC 50 values in µM concentrations. Further studies reveal that β-substituted BH bromide derived phosphonium derivatives enhance the biological activity to low µM IC 50 values. In vitrometabolic studies show that the lead candidate compound 16 inhibits the production of mitochondrial ATP, increases the proton leak within the mitochondrial membrane and abolishes the spare respiratory capacity in a concentration dependent manner., (Copyright © 2021 Elsevier Ltd. All rights reserved.)

Chrysin is a flavonoid that exists in nature and is the major component of some traditional medicinal herbs. We investigated the hepatoprotective and antihyperlipidaemic potential of chrysin against D-galactosamine (a single intraperitoneal injection 400 mg/kg BW) induced hepatotoxicity in male albino Wistar rats. D-GalN rats exhibited an increased hepato and nephro toxicity marker activities aspartate aminotransferase, alanine aminotransferase, alkaline phosphatase and gamma glutamyl transpeptidase and total bilirubin level while urea, uric acid and creatinine and lipid profile. It also negatively affected the serum total protein, albumin and A/G ratio. Rats treated with chrysin at different concentrations (25, 50 and 100 mg/kg BW) caused a significant improvement in serum protein level, decreased hepato and nephro toxicity markers. It also decreased the levels of very low density lipoprotein cholesterol and low density lipoprotein cholesterol while high density lipoprotein cholesterol significantly increased. It also decreased the levels of total cholesterol, phospholipids, triglycerides, free fatty acids in the plasma and tissues of liver and kidney. The effect of chrysin (25 mg/kg) is comparable with silymarin, a known hepatoprotective drug. Chrysin thus exhibits hepatoprotective and antihyperlipidaemic activity., (Copyright 2010 Elsevier Ltd. All rights reserved.)