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The present study was carried out to determine the effect of plant extract of Syzygium cumini and their silver nanoparticles (AgNPs) against the poultry pathogens. The plant extract was prepared in methanol, ethanol, ethyl acetate, chloroform, and n‐hexane. The results of phytochemical screening showed that the leaf extract of S. cumini have medicinally important phytochemical constituents. In the present study, AgNPs were synthesised by using an extract of S. cumini. Synthesised AgNPs were confirmed by Fourier‐transform infrared spectroscopy, ultraviolet–visible, and scanning electron microscopy. A surface plasmon resonance peak in absorption spectra showed absorption at 419 nm. The synthesised nanoparticles were found spherical in shape with the diameter range of 30–120 nm. The antimicrobial activity of crude extract and AgNPs was checked against the poultry bacterial pathogens by the agar well diffusion method. The authors' findings revealed that the crude extract and AgNPs have promising activities against all the test pathogens. It is concluded that the bioactive compounds from the extract of S. cumini and extract‐mediated AgNPs can be significantly used as an alternate poultry medicine to replace the available antibiotics, which have adverse side effects. [ABSTRACT FROM AUTHOR]

Cyclohexenone containing chalcones core is one important class of materials, which exhibit high nonlinear optical (NLO) responses and good crystallizability. The present study reports the successful development of six new fluorescent cyclohexenone derivatives (CDs) via conventional method. The molecular structures of these newly synthesized CDs were confirmed by using various such as 1H NMR, 13C NMR, FTIR, EIMS, UV-Vis spectroscopy and single crystal X-ray diffraction. The crystallographic data revealed that the spatial structure of the representative CD (4BE) belongs to monoclinic, P21/c space group. The results from luminescence studies show that the CDs molecules apparently emit intense green light at room temperature in aqueous media. The relative polarity and molecular of the CDs molecules were predicted by measuring the molecular electrostatic potential and frontier molecular orbital energy. In addition, the UV-Vis spectra, transition character and electronic structures of these CDs were computed by using quantum chemical methodology. It was interesting to note that the values of computed and experimental electronic transitions (λmax) were in good agreement and these CDs display high hyperpolarizability ( β) values. The present work will be helpful for systematical understanding of the structures and the optical properties of CDs for studying the that will suggest their potential application in . Copyright © 2015 John Wiley & Sons, Ltd. [ABSTRACT FROM AUTHOR]

The excelling role of organic chemistry in the medicinal field continues to be one of the main leads in the drug development process. Particularly, this industry requires organic chemists to discover small molecular structures with powerful pharmacological potential. Herein, a diverse range of chalcone (1-11) and aurone (12-22) derivatives was designed and synthesized and for the first time, and both motifs were evaluated as potent inhibitors of alkaline phosphatases (APs). Structural identification of the target compounds (1-22) was accomplished using common spectroscopic techniques. The effect of the nature and position of the substituent was interestingly observed and justified based on the detailed structure-activity relationship (SAR) of the target compounds against AP. It was concluded from the obtained results that all the newly synthesized compounds exhibit high inhibitory potential against the AP enzyme. Among them, compounds 12 (IC 50 = 2.163 ± 0.048 μM), 15 (IC 50 = 2.146 ± 0.056 μM), 16 (IC 50 = 2.132 ± 0.034 μM), 18 (IC 50 = 1.154 ± 0.043 μM), 20 (IC 50 = 1.055 ± 0.029 μM) and 21 (IC 50 = 2.326 ± 0.059 μM) exhibited excellent inhibitory activity against AP, and even better/more active than KH 2 PO 4 (standard) (IC 50 = 2.80 ± 0.065 μM). Remarkably, compound 20 (IC 50 = 1.055 ± 0.029 μM) may serve as a lead structure to design more potent inhibitors of alkaline phosphatase. To the best of our knowledge, these synthetic compounds are the most potent AP inhibitors with minimum IC 50 values reported to date. Furthermore, a molecular modeling study was performed against the AP enzyme (1EW2) to check the binding interaction of the synthesized compounds 1-22 against the target protein. The Lineweaver-Burk plots demonstrated that most potential derivative 20 inhibited h-IAP via a non-competitive pathway. Finally, molecular dynamic (MD) simulations were performed to evaluate the dynamic behavior, stability of the protein-ligand complex, and binding affinity of the compounds, resulting in the identification of compound 20 as a potential inhibitor of AP. Accordingly, excellent correlation was observed between the experimental and theoretical results. The pharmacological studies revealed that the synthesized analogs 1-22 obey Lipinski's rule. The assessment of the ADMET parameters showed that these compounds possess considerable lead-like characteristics with low toxicity and can serve as templates in drug design., Competing Interests: There are no conflicts to declare., (This journal is © The Royal Society of Chemistry.)

Breast cancer is among the frequently occurring cancer worldwide. The foremost underline aim of this study was to determine the growth inhibitory effect along with mechanistic study of a Bruguiera gymnorrhiza extract on MCF-7. The cytotoxicity activity was determined by using the MTS assay. Butanol extract exhibited the maximum cytotoxicity activity against the MCF-7 cells with IC 50 of 3.39 μg/mL, followed by diethyl ether and methanol extract (IC 50 at 16.22 μg/mL and 37.15 μg/mL, respectively) at 72 h. The DeadEnd TM Colorimetric Apoptosis Detection System confirmed the induction of apoptosis (via DNA fragmentation) in MCF-7 cells. Both butanol and diethyl ether extracts of B. gymnorrhiza significantly increase the caspase-3 level. However, the diethyl ether extract induced higher caspase-9 levels compared to caspase-8, suggesting that the intrinsic pathway was the major route in the process of apoptosis. Thin-layer chromatography profiling demonstrated the presence of phenolic, terpene, and alkaloid compounds in crude methanol, diethyl ether, and butanol extracts. The phytochemicals present in the extracts of B. gymnorrhiza might have the potential to be a future therapeutic agent against breast cancer., Competing Interests: There are no conflicts of interest., (Copyright: © 2020 Journal of Advanced Pharmaceutical Technology & Research.)

Cancer is a complex multifactorial disease and leading causes of death worldwide. Despite the development of many anticancer drugs, there is a reduced survival rate due to severe side effects. The nontargeted approach of convention drugs is one of the leading players in context to toxicity. Hyaluronan is a versatile bio-polymer and ligand of the receptor (CD44) on cancer cells. The MCF-7 and HT-29 cancer cell lines treated with hyaluronic acid-paclitaxel (HA-PTX) showed the distinguishing morphological features of apoptosis. Flow cytometric analysis showed that HA-PTX induces apoptosis as a significant mode of cell death. The activation level of tumor suppressor protein (p53) increased after PTX treatment in MCF-7, but no changes observed in HT-29 might be due to hereditary mutations. The lack of suppression in AKT and Rho A protein suggest the use of possible inhibitors in future studies which might could play a role in increasing the sensitivity of drug towards mutated cells line and reducing the possibilities for cancer cell survival, migration, and metastasis., Competing Interests: There are no conflicts of interest., (Copyright: © 2020 Journal of Advanced Pharmaceutical Technology & Research.)