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21.
Sridevi Duggirala Rakesh P. Nankar Selvakumar Rajendran Mukesh Doble 《Applied biochemistry and biotechnology》2014,174(1):283-296
Naturally occurring phytochemicals with reported antibacterial activity were screened for their ability to inhibit the bacterial cell division protein Escherichia coli FtsZ. Among the representative compounds, coumarins inhibit the GTPase and polymerization activities of this protein effectively. Further screening with ten coumarin analogs we identified two promising candidates, scopoletin and daphnetin. The former is found to inhibit the GTPase activity of the protein in a noncompetitive manner. Docking of these coumarins with the modeled protein indicate that they bind to T7 loop, which is different from the GTP-binding site (active site), thereby supporting the experimental data. Lowest binding energy is obtained with scopoletin. 3D QSAR indicates the need for groups such as hydroxyl, diethyl, or dimethyl amino in the 7th carbon for enhanced activity. None of the coumarins exhibited cytotoxicity against NIH/3T3 and human embryonic kidney cell lines. The length of Bacillus subtilis increases in the presence of these compounds probably due to the lack of septum formation. Results of this study indicate the role of coumarins in halting the first step of bacterial cell division process. 相似文献
22.
Neha Batra Vinoth Rajendran Ishan Wadi Ankit Lathwal Roshan Kumar Dutta Prahlad C. Ghosh Rinkoo D. Gupta Mahendra Nath 《Journal of heterocyclic chemistry》2020,57(4):1625-1636
A series of benzenesulfonamide-appended [1,2,3]-triazole hybrids was synthesized by using [3 + 2] cycloaddition of primary, secondary, and tertiary sulfonamide azides with various phenoxymethylacetylenes under click reaction conditions. After structural characterization, the compounds were subjected to in-silico absorption, distribution, metabolism, excretion and toxicity (ADMET) screening to evaluate their drug-likeness and other pharmacokinetic parameters. Furthermore, their in vitro antiplasmodial potential was assessed against Plasmodium falciparum (3D7) strain, and some of the synthesized compounds displayed promising antimalarial potency. On cytotoxicity evaluation using MTT cell viability assay, the most active candidate N-(4,6-dimethylpyridin-2-yl)-4-(4-(4-nitrophenoxy)methyl)-1H-[1,2,3]-triazol-1-yl)benzenesulfonamide ( 14 ; IC50 6.2 μg/mL) demonstrated CC50 7.5 μg/mL against human hepatocarcinoma (HUH-7) cells. 相似文献
23.
Rajendran Duraisamy Ramalingam Ganapathy Sundaram Esakkimuthu Jawahar Paulraj Sivakumar Vaithilingam Mahian Omid Bellos Evangelos 《Journal of Thermal Analysis and Calorimetry》2020,140(1):33-51
Journal of Thermal Analysis and Calorimetry - The solar collector (reflector and receiver) is the primary device being used in the concentrating solar power technologies for tapping the solar... 相似文献
24.
Simultaneous Delamination and Rutile Formation on the Surface of Ti3C2Tx MXene for Copper Adsorption
In this work, we studied the formation of the rutile phase of titanium dioxide (TiO2) on delaminated MXene (d‐Ti3C2Tx) flakes by the reaction of Ti3C2Tx with amino acids in water. Three types of amino acids with varied side‐chain polarity were used to delaminate Ti3C2Tx. d‐Ti3C2Tx flakes formed stable colloidal solutions due to the negative surface charges of chemisorbed amino acids on the d‐Ti3C2Tx. Rutile formed on d‐Ti3C2Tx at room temperature upon the intercalation of aromatic amino acids and subsequent sonication of the solution, while flakes intercalated with aliphatic amino acids did not oxidize. X‐Ray diffraction (XRD), transmission electron microscopy (TEM) and Raman spectroscopy revealed the nanosize rutile formation on the surface of Ti3C2Tx flakes. The XPS results indicated the surface functionalization of histidine on d‐Ti3C2Tx flakes. As‐synthesized histidine functionalized rutile TiO2@d‐Ti3C2Tx hybrid was used for adsorption of Cu2+ ions from aqueous solution with a maximum uptake of 95 mg g?1. 相似文献
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26.
Devipriya Balu Kumaradhas Poomani Kalyanam Nagabushanam Sridhar Balasubramanium Rajendran Ramanujam Majeed Muhammed 《Journal of chemical crystallography》2011,41(5):697-702
Abstract
5-Lipoxygenase inhibitor 3-O-acetyl-9,11-dehydro-β-boswellic acid was detected in the extract of Boswellia serrata gum resulting from unstable 11-hydroxy precursor. It was reported more potent than other Boswellic acids in its inhibition of 5-Lipoxygenase. Here, we report the method of conversion of 3-acetoxy-β-boswellic acid to 3-O-acetyl-9,11-dehydro-β-boswellic acid, and the crystal structure of later. This compound crystallizes in orthorhombic space group P212121 with cell parameters of a = 12.726(1) ?, b = 16.597(1) ?, c = 27.332(2) ?, α = β = γ = 90°, V = 5772.7(5) ?3, D c = 1.143 Mg/m3, and Z = 8. The X-ray structure investigation indicates that the rings A, B, D and E are exhibit chair and the ring C adopts a distorted half chair conformation. The conformational difference of the two structures in the arrangement is due to crystal packing of 3-O-acetyl-9,11-dehydro-β-boswellic acid. The molecular packing is stabilized by C–H···O and O–H···O types of hydrogen bonding interactions. 相似文献27.
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29.
Polymer electrolyte films prepared from poly (methyl methacrylate) and LiAsF6 with different concentrations of plasticizer (DBP) are described. The formation of polymer-salt complexes has been confirmed
by XRD and FTIR spectral studies. The temperature dependence of the conductivity of the polymer films obeys the VTF relation.
Values of conductivities of the polymer complexes are presented and discussed. 相似文献
30.