48 research outputs found

    The Synthesis and Strecker Reaction of 2‑Chlorotetrafluoroethanesulfinyl Ketimines

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    A series of 2-chlorotetrafluoroethanesulfinyl ketimines were prepared from 2-chlorotetrafluoroethanesulfinamide and ketones in high yields, and their Strecker reactions with TMSCN have been investigated. High yields and excellent diastereoselectivities were achieved in the presence of a catalytic amount of CsF under mild conditions. The six-membered chairlike models were proposed to account for the high stereoselective Strecker reaction

    The characteristics of the patients with type 2 diabetes (N = 960).

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    <p>The characteristics of the patients with type 2 diabetes (N = 960).</p

    The relationships between PACIC scores and different self-management behaviors (N = 960).

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    <p>The relationships between PACIC scores and different self-management behaviors (N = 960).</p

    The relationships between PACIC and the most often utilized medical institutions for monitoring and treating diabetes among the patients with type 2 diabetes (N = 960).

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    <p>The relationships between PACIC and the most often utilized medical institutions for monitoring and treating diabetes among the patients with type 2 diabetes (N = 960).</p

    The relationships between different self-management behaviors and glycemic control, and the relationships between PACIC and glycemic control (N = 960).

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    <p>The relationships between different self-management behaviors and glycemic control, and the relationships between PACIC and glycemic control (N = 960).</p

    Label-Free Luminescent Switch-On Probe for Ochratoxin A Detection Using a G‑Quadruplex-Selective Iridium(III) Complex

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    A library of six luminescent Ir­(III) complexes were synthesized and studied for their capacity to function as probes for G-quadruplex DNA. The novel Ir­(III) complex <b>1</b> was discovered to be selective for G-quadruplex structures and was subsequently used for the construction of a label-free G-quadruplex-based ochratoxin A (OTA) sensing platform in aqueous solution. The assay exhibited linearity for OTA in the range of 0 to 60 nM (<i>R</i><sup>2</sup> = 0.9933), and the limit of detection for OTA was 5 nM. Furthermore, this assay was highly selective for OTA over its structurally related analogues

    Synthesis, characterization and <i>in vitro</i> antitumor behavior of a vanadium(V) complex with 4′-(3-methoxyphenyl)-2,2′:6′2″-terpyridine

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    <p>A dioxovanadium(V) complex, [VO<sub>2</sub>(moptpy)](ClO<sub>4</sub>) (<b>1</b>, moptpy = 4′-(3-methoxyphenyl)2,2′:6′2″-terpyridine), was synthesized and characterized by elemental analysis, ESI-MS, UV–vis, IR, and <sup>1</sup>H, <sup>13</sup>C, and <sup>51</sup>V NMR. The cytotoxicity <i>in vitro</i> of <b>1</b> was evaluated against cancer cell lines HepG-2 (hepatocellular carcinoma), SGC-7901 (gastric carcinoma), SiHa (cervical cancer), BEL-7402 (hepatocellular), and rat PC-12 (pheochromocytoma) by the MTT method. The results demonstrated that <b>1</b> exhibits superior anticancer activity <i>in vitro</i> with much lower values of 50% inhibitive concentration (IC<sub>50</sub>) against the selected cell lines than cisplatin, and <b>1</b> shows the highest cytotoxic activity toward SGC-7901 cells (IC<sub>50</sub> = 1.3 ± 0.1 μM) among the selected cell lines. A series of cellular morphological and staining experiments were carried out, and the results indicated that <b>1</b> can effectively induce apoptosis of SGC-7901 cells through a ROS-mediated mitochondrial dysfunction pathway. In addition, cellular incorporation and cell cycle analysis were also performed, and it was concluded from the experimental observations that <b>1</b> can efficiently enter into the cell nuclei, and the complex inhibits cell growth in SGC-7901 cell at G0/G1 phase.</p
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