46 research outputs found
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Protein sequences of the ABCA transporters of the eight species. (XLSX 25 kb
Solubility of the Schiff Base Ligand and the Organoaluminum Supported by the Ligand in Pure Solvents: Characterization, Determination, Analysis, and Model Correlation
Schiff bases and organoaluminum compounds have wide applications
in medicine and catalysis. TG-DSC provided melting points and melting
enthalpies for the Schiff base ligand (1, 2-[[(2,6-difluorophenyl)Âimino]Âmethyl]Âphenol,
CAS: 26672-04-8), with Tm at 349.55 K and ΔHfus at 22.797 kJ/mol, and for the organoaluminum compound supported
by the ligand (2, [2-[[(2,6-difluorophenyl)Âimino]Âmethyl]Âphenoxy]Âdimethylaluminum,
CAS: 2851050-89-8), with Tm at 396.04 K and ΔHfus at 11.137 kJ/mol. The range of molecular electrostatic potentials
for the two compounds was obtained by molecular electrostatic potential
analysis, with the potential range for compound 1 being
from +95.1 kJ/mol to −133.2 kJ/mol and that for compound 2 being from +139.9 kJ/mol to −132.7 kJ/mol. Hirshfeld
surface analysis indicated that H···H contacts were
the dominant contact interactions in these two molecules. In addition,
the solubilities of the two compounds in 11 pure solvents were determined,
and experimental data were correlated using 7 thermodynamic equations.
The results displayed that the NRTL model had the best correlation
result for the two compounds. These experimental results will have
significant implications for the purification, crystallization, and
industrial applications of similar types of substances
Electrophilic <i>N</i>‑Trifluoromethylation of N–H Ketimines
A direct <i>N</i>-trifluoromethylation
method has been
developed by the use of the <i>in situ</i> generated [ArICF<sub>3</sub>]<sup>+</sup> species as the electrophilic trifluoromethyl
source. Upon treatment of N–H ketimines with Ruppert–Prakash
reagent in the presence of PhIÂ(OAc)<sub>2</sub> and KF, or with Togni’s
reagent II catalyzed by copper salt, <i>N</i>-trifluoromethylated
imine products were obtained in moderate to good yields
A new sesquiterpene from the entomogenous fungus <i>Phomopsis amygdali</i>
<div><p>A new sesquiterpene, (+)-<i>S</i>-1-methyl-abscisic-6-acid (<b>1</b>), together with five known compounds, (+)-<i>S</i>-abscisic acid (<b>2</b>), fusicoccin J (<b>3</b>), 3α-hydroxyfusicoccin J (<b>4</b>), (<i>R</i>)-5-hydroxymethylmellein (<b>5</b>) and 4-hydroxyphenethyl acetate (<b>6</b>) was isolated from the fermentation extract of <i>Phomopsis amygdali</i>, an entomogenous fungus isolated from <i>Call midge</i>. Their structures were determined mainly by analysis of MS and NMR spectroscopic data. Compounds <b>1</b>–<b>6</b> were tested for antimicrobial activity against three plant pathogenic fungi: <i>Gibberella zeae</i>, <i>Verticillium albo-atrum</i>, and <i>Fusarium nivale</i>, and two bacteria: <i>Escherichia coli</i> and <i>Pseudomonas aeruginosa</i> 2033E. As a result, compounds <b>1</b>–<b>4</b> displayed antibacterial activity against Gram-negative <i>P. aeruginosa</i> 2033E, and the minimum inhibition concentration (MIC value) of <b>1</b>–<b>4</b> is 30 μg/mL, 58 μg/mL, 26 μg/mL, and 26 μg/mL, respectively.</p></div
Effect of Dicarboxylate Ligands on the Construction of Cd(II) Complexes Based on a Flexible Bis-Triazole Ligand
<div><p>In this work, two dicarboxylate ligands, 4,4′-oxybis(benzoic acid) (H<sub>2</sub>oba) and 4,4′-biphenyldicarboxylic acid (H<sub>2</sub>bpdc) were employed as coligands to perform a comparison on the structures of Cd(II)-btmx complexes (btmx = 1,4-bis(1,2,4-triazol-1-ylmethyl)-2,3,5,6-tetramethylbenzene) motifs. Two new complexes, {[Cd(btmx)(oba)]·H<sub>2</sub>O}<sub>n</sub> (1) and [Cd(btmx)(bpdc)]<sub>n</sub> (2), have been synthesized and characterized. Structural analyses show that 1 shows a 1D double-chain, while 2 displays an undulating 2D 4<sup>4</sup>-<i>sql</i> network with 2-fold interpenetration. The structural differences of the two complexes suggest that the dicarboxylate ligands have great impact on the formation of such coordination architectures. Furthermore, the photoluminescence properties of 1 and 2 have also been investigated.</p></div
Reactivity Studies of LAlH<sub>2</sub> (L = HC(CMeNAr)<sub>2</sub>, Ar = 2,6‑<i>i</i>Pr<sub>2</sub>C<sub>6</sub>H<sub>3</sub>) with 2‑Aminobenzenethiol, 2‑Aminophenol, and 1,4-Dithiane-2,5-diol
The reaction of LAlH<sub>2</sub> (L = HCÂ(CMeNAr)<sub>2</sub>, Ar
= 2,6-<i>i</i>Pr<sub>2</sub>C<sub>6</sub>H<sub>3</sub>)
(<b>1</b>) with 2-aminobenzenethiol, 2-aminophenol, and 1,4-dithiane-2,5-diol
resulted in the compounds LAlÂ[(μ<i>-</i>N)Â(μ<i>-</i>S)]Â(<i>o</i>-C<sub>6</sub>H<sub>4</sub>) (<b>2</b>), LAlÂ[(μ<i>-</i>O)Â(<i>o</i>-C<sub>6</sub>H<sub>4</sub>)Â(NH<sub>2</sub>)]<sub>2</sub> (<b>3</b>), and LAlÂ(μ<i>-</i>O)<sub>2</sub>(<i>p</i>-dithiane) (<b>4</b>), respectively. Compound <b>2</b> features an organic–inorganic hybrid containing an NAlSC<sub>2</sub> five-membered ring, while compound <b>3</b> exhibits
a C–O–Al–O–C chain structure. Compound <b>4</b> forms a basket-like molecule with the C<sub>4</sub>S<sub>2</sub> unit as the bottom part and O<sub>2</sub>Al as the handle.
Complexes <b>2</b>, <b>3</b>, and <b>4</b> were
characterized by <sup>1</sup>H NMR, elemental analysis, and single-crystal
X-ray diffraction studies
Aluminum Complexes Containing the C–O–Al–O–C Framework as Efficient Initiators for Ring-Opening Polymerization of ε‑Caprolactone
Three aluminum complexes, LAlÂ(OCH<sub>2</sub>C<sub>6</sub>H<sub>4</sub>-2-NH<sub>2</sub>)<sub>2</sub> (<b>2</b>), LAlÂ(9-OC<sub>13</sub>H<sub>9</sub>)<sub>2</sub> (<b>3</b>), and LAlÂ(OC<sub>6</sub>H<sub>10</sub>-4-NH<sub>2</sub>)<sub>2</sub> (<b>4</b>), were synthesized in good yield by reacting
one equivalent of LAlH<sub>2</sub> (<b>1</b>) (L = HCÂ(CMeNAr)<sub>2</sub>, Ar = 2,6-<i>i</i>Pr<sub>2</sub>C<sub>6</sub>H<sub>3</sub>) with two equivalents
of 2-aminobenzyl alcohol, 9-hydroxyfluorene, and <i>trans</i>-4-aminocyclohexanol, respectively. All complexes (<b>2</b>, <b>3</b>, and <b>4</b>) contain the C–O–Al–O–C
framework. These complexes have been characterized by IR, <sup>1</sup>H and <sup>13</sup>C NMR, elemental analyses, and single-crystal
X-ray structural analysis. Furthermore, the excellent catalytic activities
of <b>2</b>, <b>3</b>, and <b>4</b> for ring-opening
polymerization of ε-caprolactone in the presence of isopropyl
alcohol were investigated
Reactivity Studies of LAlH<sub>2</sub> (L = HC(CMeNAr)<sub>2</sub>, Ar = 2,6‑<i>i</i>Pr<sub>2</sub>C<sub>6</sub>H<sub>3</sub>) with 2‑Aminobenzenethiol, 2‑Aminophenol, and 1,4-Dithiane-2,5-diol
The reaction of LAlH<sub>2</sub> (L = HCÂ(CMeNAr)<sub>2</sub>, Ar
= 2,6-<i>i</i>Pr<sub>2</sub>C<sub>6</sub>H<sub>3</sub>)
(<b>1</b>) with 2-aminobenzenethiol, 2-aminophenol, and 1,4-dithiane-2,5-diol
resulted in the compounds LAlÂ[(μ<i>-</i>N)Â(μ<i>-</i>S)]Â(<i>o</i>-C<sub>6</sub>H<sub>4</sub>) (<b>2</b>), LAlÂ[(μ<i>-</i>O)Â(<i>o</i>-C<sub>6</sub>H<sub>4</sub>)Â(NH<sub>2</sub>)]<sub>2</sub> (<b>3</b>), and LAlÂ(μ<i>-</i>O)<sub>2</sub>(<i>p</i>-dithiane) (<b>4</b>), respectively. Compound <b>2</b> features an organic–inorganic hybrid containing an NAlSC<sub>2</sub> five-membered ring, while compound <b>3</b> exhibits
a C–O–Al–O–C chain structure. Compound <b>4</b> forms a basket-like molecule with the C<sub>4</sub>S<sub>2</sub> unit as the bottom part and O<sub>2</sub>Al as the handle.
Complexes <b>2</b>, <b>3</b>, and <b>4</b> were
characterized by <sup>1</sup>H NMR, elemental analysis, and single-crystal
X-ray diffraction studies
α5-nAChR/AKT signaling involved in anti-apoptotic effects of nicotine in cisplatin-induced apoptosis of BGC823 cells.
<p>A: P-AKT was activated after exposure to 100μM nicotine in BGC823 cells (lane 2 and lane3). Cisplatin strongly suppressed activity of P-AKT (lane 1 and lane 2) but nicotine also induced P-AKT in the presence of cisplatin (lane 2 and lane 3). Down-regulation of α5-nAChR expression decreased the level of P-AKT (lane 4 and lane 5). Treatment with LY294002 downregulated P-AKT expression (lane 3 and lane 5). Combination LY294002 with si-CHRNA5 transfection significantly repressed the nicotine induced P-AKT protein levels (lane 3 and lane 6); *p<0.05; B: Cisplatin induced an increase in caspase-3 and Bax activation in BGC823 cells a decrease in Bcl-2 and Survivin expressions, whereas nicotine blocked cisplatin- induced Bcl-2, Bax, caspase-3 and Survivin expressions; With silence of α5-nAChR co-administrated LY294002, an increased apoptosis was observed with the induction of Bcl-2, Bax, Survivin and Caspase-3 by nicotine in BGC823 cells. *p<0.05; C: Assessment of apoptosis by AnnexinV/7-AAD staining in each group. BGC823 cells were pre-treated with 100 μM nicotine and cisplatin for 24 h, and/or si-α5-nAChR for 48h, and/or AKT inhibitor LY294002 for 24h, and harvested.</p
Characterization of <i>mcm3<sub>K499R</sub></i>, <i>mcm3<sub>K499N</sub></i>, and <i>mcm3<sub>K499Q</sub></i> alleles.
<p>(A) The <i>MCM3</i>, <i>mcm3<sub>K499R</sub></i>, <i>mcm3<sub>K499N</sub></i>, and <i>mcm3<sub>K499Q</sub></i> genes encoded on <i>LEU2</i>-containing centromeric plasmids, or empty plasmid (vector), were transformed into MDY16 (<i>mcm3</i>Δ YCplac33-<i>MCM3</i>). The transformed yeast were grown overnight at 30°C in liquid YPD, serially diluted, and spotted onto YPD, synthetic complete lacking leucine, and YPD containing 5-FOA. (B) The <i>MCM3</i> and <i>mcm3<sub>K499R</sub></i> plasmid-shuffled strains were grown overnight at 30°C, serially diluted and spotted on YPD and YPD containing 0.03% MMS, 200 mM hydroxyurea (HU), or 20 mM caffeine. The <i>mec2-1</i> strain was subjected to the same growth assay as a positive control for genotoxic stress <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0082177#pone.0082177-Weinert1" target="_blank">[51]</a>. (C) The <i>MCM3</i> and <i>mcm3<sub>K499R</sub></i> plasmid-shuffled strains were grown overnight at 30°C, serially diluted, spotted on YPD, and grown at 16°C, 30°C or 37°C.</p