Research Notes : United States : Evaluation of soybean germplasm for stress tolerance and biological efficiency : To evaluate soybean germplasm and cultivars for stress tolerance toward - Pest and Diseases

A total of 1,273 soybean germplasm lines and 39 commercial varie-ties were screened for natural resistance to Mexican bean beetle (MBB) under field conditions. There were 421, 314, 266, 136, and 136 germplasm and varieties from maturity groups VI, VII, VIII, IX, and X, respectively. An average of 1,000 laboratory-reared adult MBB per day were released uniformly over all the field throughout the growing season from May until September to create an adequate MBB infestation

Research Notes : United States : Evaluation of soybean germplasm for stress tolerance and biological efficiency towards : Pests

One of the major objectives of the proposal is systematic screening of all available soybean germplasm of Maturity Groups III to VIII for a natural resistance to a major insect pest, the Mexican bean beetle (MBB). These six Maturity Groups (III-VIII) cover abouL 5,000 plant introductions (Pis), 350 commercial varieties, and 80 breeding lines. Selected accessions of the most resistant (35% or less leaf defoliation) and highly susceptible (over 75% leaf defoliation) in general screening under field conditions were re-evaluated in triplicate in 1985 and in quadruplicate in 1986 (Table 2). About 20 special selections were evaluated for MBB under controlled environmental conditions

3D-MID Technology for surface modification of polymer-based composites: a comprehensive review

The three-dimensional molded interconnected device (3D-MID) has received considerable attention because of the growing demand for greater functionality and miniaturization of electronic parts. Polymer based composite are the primary choice to be used as substrate. These materials enable flexibility in production from macro to micro-MID products, high fracture toughness when subjected to mechanical loading, and they are lightweight. This survey proposes a detailed review of different types of 3D-MID modules, also presents the requirement criteria for manufacture a polymer substrate and the main surface modification techniques used to enhance the polymer substrate. The findings presented here allow to fundamentally understand the concept of 3D-MID, which can be used to manufacture a novel polymer composite substrate

A Nano-Mgo and Ionic Liquid-Catalyzed ‘Green’ Synthesis Protocol for the Development of Adamantyl-Imidazolo-Thiadiazoles as Anti-Tuberculosis Agents Targeting Sterol 14α-Demethylase (CYP51)

In this work, we describe the ‘green’ synthesis of novel 6-(adamantan-1-yl)-2-substitutedimidazo[2,1-b][1,3,4]thiadiazoles (AITs) by ring formation reactions using 1-(adamantan-1-yl)-2-bromoethanone and 5-alkyl/aryl-2-amino1,3,4-thiadiazoles on a nano material base inionic liquid media. Given the established activity of imidazothiadiazoles against M. tuberculosis,we next examined the anti-TB activity of AITs against the H37Rv strain using Alamarblue assay. Among the tested compounds 6-(adamantan-1-yl)-2-(4-methoxyphenyl)imidazo[2,1-b][1,3,4]thiadiazole (3f) showed potent inhibitory activity towards M. tuberculosis with an MIC value of 8.5 μM. The inhibitory effect of this molecule against M. tuberculosis was comparable to the standard drugs such as Pyrazinamide, Streptomycin, and Ciprofloxacin drugs. Mechanistically, an in silico analysis predicted sterol 14α-demethylase (CYP51)as the likely target and experimental activity of 3f in this system corroborated the in silico target prediction. In summary, we herein report the synthesis and biological evaluation of novel AITs against M. tuberculosis that likely target CYP51 to induce their antimycobacterial activity

A nano-MgO and ionic liquid-catalyzed 'green' synthesis protocol for the development of adamantyl-imidazolo-thiadiazoles as anti-tuberculosis agents targeting sterol 14α-demethylase (CYP51)

In this work, we describe the 'green' synthesis of novel 6-(adamantan-1-yl)-2-substitutedimidazo2,1-b1,3,4thiadiazoles (AITs) by ring formation reactions using 1-(adamantan-1-yl)-2-bromoethanone and 5-alkyl/aryl-2-amino1,3,4-thiadiazoles on a nano material base in ionic liquid media. Given the established activity of imidazothiadiazoles against M. tuberculosis, we next examined the anti-TB activity of AITs against the H37Rv strain using Alamar blue assay. Among the tested compounds 6-(adamantan-1-yl)-2-(4-methoxyphenyl)imidazo2,1-b1,3,4thiadiazole (3f) showed potent inhibitory activity towards M. tuberculosis with an MIC value of 8.5 μM. The inhibitory effect of this molecule against M. tuberculosis was comparable to the standard drugs such as Pyrazinamide, Streptomycin, and Ciprofloxacin drugs. Mechanistically, an in silico analysis predicted sterol 14α-demethylase (CYP51) as the likely target and experimental activity of 3f in this system corroborated the in silico target prediction. In summary, we herein report the synthesis and biological evaluation of novel AITs against M. tuberculosis that likely target CYP51 to induce their antimycobacterial activity. © 2015 Anusha et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited

Nano-​cuprous oxide catalyzed one-​pot synthesis of a carbazole-​based STAT3 inhibitor: a facile approach via intramolecular C-​N bond formation reactions

In this study, we report the one-​pot synthesis of substituted carbazole derivs. using nano cuprous oxide as a catalyst via intramol. C-​N bond forming reactions. Among the synthesized carbazoles, 3'-​((3-​acetyl-​6-​chloro-​9H-​carbazol-​9-​yl)​methyl)​-​[1,​1'-​biphenyl]​-​2-​carbonitrile (ACB) was identified as a lead antiproliferative agent against lung cancer cell lines A549 and LLC with an IC50 of 13.6 and 16.4 μM resp. Furthermore, we found that the lead compd. suppresses the constitutive phosphorylation of STAT3 (Tyr-​705) in A549, HCC-​2279 and H1975 cells. We analyzed the levels of phospho-​STAT3 and LSD1 in the nuclear ext. of ACB treated HCC-​2279 cells to evaluate the transcriptional activity of STAT3. We found the downregulation of phospho-​STAT3 without any change in the expression of LSD1 indicating that ACB downregulates the transcriptional activity of STAT3. Mol. docking anal. revealed that ACB makes a favorable interaction with Arg-​609 and Ser-​613 in the pTyr site of the SH2 domain of STAT3

LEMONGRASS PLANT LEAF AND CULM AS POTENTIAL SOURCES OF REINFORCEMENT FOR BIO-COMPOSITES

A possible source of natural reinforcement for bio-composites can be represented by lemongrass plant (Cymbopogon flexuosus), a clumped and perennial grass which belongs to the Poaceae family. This plant is extensively used for several applications such as pharmacology, food preservation and cosmetics but, to the best of our knowledge, few papers were published on its use as source for reinforcement of composites and no one article was focused on the comparison between lemongrass leaves and culms as potential source of natural reinforcement. To this aim, a preliminary investigation on leaf and culm fibers was carried out to compare their physical and chemical features as well as their tensile properties. Furthermore, bio-composites based on a biodegradable starch-derived matrix (MaterBi®) and lemongrass leaf and culm particles were manufactured via extrusion and compression molding. For both fillers, two compositions (i.e., 10% and 20 wt.%) were investigated in terms of morphological and mechanical properties

Kinetics and mechanism of oxidation of erythro-series pentoses and hexoses by N-chloro-p-toluenesulfonamide

The kinetics and mechanism of oxidation of D-glucose, D-mannose, D-fructose, D-arabinose, and D-ribose with chloramine-T in alkaline medium were studied. The rate law, rate = k Chloramine-T] Sugar] HO-](2), was observed. The rate of the reaction was influenced by a change in ionic strength of the medium, and the dielectric effect was found to be negative. The latter enabled the computation of d(AB), the size of the activated complex. The reaction rate was almost doubled in deuterium oxide. Activation energies were calculated from the Arrhenius plots. HPLC and GLC-MS analyses of the products indicated that the sugars were oxidized to a mixture of aldonic acids, consisting of arabinonic, ribonic, erythronic, and glyceric acids. Based on these data, a plausible mechanism involving the aldo-enolic anions of pentoses and keto-enolic anions of hexoses is suggested. (C) 1998 Elsevier Science Ltd. All rights reserved

Adamantyl-tethered-biphenylic compounds induce apoptosis in cancer cells by targeting Bcl homologs

Bcl homologs prominently contribute to apoptotic resistance in cancer cells and serve as molecular targets in treatment of various cancers. Herein, we report the synthesis of biphenyl-adamantane derivatives by a ligand free palladium on carbon based Suzuki reaction using diisopropylamine as a base for the coupling of adamantane based aryl chloride with a variety of aryl boronic acids. Among the biphenyl derivatives synthesized, compound 3'-(adamantan-1-yl)-4'-methoxy-1,1'-biphenyl-3-ol (AMB) displayed cytotoxic activity against hepatocellular carcinoma cell lines without significantly affecting the normal cell lines. Further, AMB caused increased accumulation of the HCC cells in subG1 phase, decreased the expression of Bcl-2, Bcl-xL, cyclin D1, caspase-3, survivin and increased the cleavage of PARP in a time-dependent manner. In silico molecular interaction studies between Bcl homologs and AMB showed that the biphenyl scaffold is predicted to form �-� interactions with Phe-101 and Tyr-105 and the adamantyl fragment is predicted to occupy another hydrophobic region in the kink region of the binding groove. In summary, we report on the synthesis and biological characterization of adamantyl-tethered biphenylic compounds that induce apoptosis in tumor cells most likely by targeting Bcl homologs. © 2015 Elsevier Ltd