8,164 research outputs found

    1-(2-Hy­droxy­benzo­yl)thio­semicarbazide hemihydrate

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    The asymmetric unit of the title compound, C8H9N3O2S·0.5H2O, contains two thiosemicarbazide mol­ecules with the short distance of 3.521 (3) Å between the centroids of the benzene rings, and one water mol­ecule. In the two independent mol­ecules, the benzene rings and the thio­semicarbazone fragments are twisted at 9.2 (3) and 18.5 (3)°. An extensive three-dimensional hydrogen-bonding network, formed by inter­molecular N—H⋯O, N—H⋯S and O—H⋯O hydrogen bonds, consolidates the crystal packing

    Proteomic identification of differentially expressed and phosphorylated proteins in epidermis involved in larval-pupal metamorphosis of Helicoverpa armigera

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    <p>Abstract</p> <p>Background</p> <p>Metamorphosis is an important process in the life cycle of holometabolous insects and is regulated by insect hormones. During metamorphosis, the epidermis goes through a significant transformation at the biochemical and molecular levels.</p> <p>Results</p> <p>To identify proteins and phosphoproteins involved in this process, we separated and compared epidermal protein profiles between feeding larvae and metamorphically committed larvae using two-dimensional gel electrophoresis and Pro-Q Diamond Phosphoprotein Staining. Sixty-one spots showing differential expression and/or phosphorylation were analyzed by mass spectrometry and eighteen proteins were proved related to larval-pupal transformation. Eight of them were further examined at the mRNA level by Reverse Transcription Polymerase Chain Reaction (RT-PCR) and two of them were examined at the protein level by Western blot. Calponin was highly expressed in the metamorphic epidermis and phosphorylated by protein kinase C.</p> <p>Conclusion</p> <p>Our results suggest that the expression and phosphorylation of these proteins may play important roles in coordinating the biochemical processes involved in larval-pupal metamorphosis.</p

    Incidence of central nervous system metastases in patients with human epidermal growth factor receptor 2-positive metastatic breast cancer treated with trastuzumab: A meta-analysis

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    This study aimed to estimate the incidence of central nervous system (CNS) metastases in patients with human epidermal growth factor receptor 2 (HER2)-positive metastatic breast cancer (MBC) treated with trastuzumab. Studies were identified through a literature search of electronic databases. Random-effects meta-analyses were performed to estimate the incidence rate of CNS metastases, trastuzumab therapy duration, and time from trastuzumab therapy to CNS metastasis diagnosis. A meta-analysis of odds ratios was performed to evaluate the significance of a difference in CNS metastasis incidence between patients with and without trastuzumab treatment. Thirty studies (8121 trastuzumab-treated and 3972 control patients) were included. The follow-up duration was 18.9 months (95% confidence interval [CI]: 13.8, 24.1). The trastuzumab treatment duration was 9.0 months (95% CI: 7.0, 11.0). The median interval between the start of trastuzumab therapy and CNS metastasis diagnosis was 12.2 months (95% CI: 9.5, 14.7). The incidence of CNS metastasis after the start of trastuzumab therapy was 22% (95% CI: 16, 27). The incidence of CNS metastases was significantly higher in trastuzumab-treated than in non-trastuzumab-treated patients (odds ratio: 1.39 [95% CI: 1.06, 1.82],&nbsp;p=0.02). The survival time from the start of the study was 23.4 months (95% CI: 19.7, 27.1) in trastuzumab-treated patients and 18.4 months (95% CI: 12.7, 24.1) in patients treated with control regimens. The survival time after the development of CNS metastases in trastuzumab-treated patients was 19.2 months (95% CI: 15.6, 25.9). Approximately 22% of patients with HER2-positive MBC who were treated with trastuzumab developed CNS metastases. However, trastuzumab-treated patients had a longer survival than patients who were not treated with trastuzumab

    Simultaneous determination of ten compounds in two main medicinal plant parts of Tibetan herb, Pterocephalus hookeri (CB Clarke) Höeck, by ultra-high performance liquid chromatography-photodiode array

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    Purpose: To develop an ultra-high performance liquid chromatography (UPLC) - photodiode array (PDA) method to compare the chemical composition of two different medicinal components of Pterocephalus hookeri.Methods: Samples were chromatographically separated in succession using Waters Acquity UPLCR BEH C18 column (2.1 × 100 mm, 1.7 μm) and gradient elution (0.2 % phosphoric acid aqueous -acetonitrile). Using partial least squares discriminant analysis and one-way analysis of variance, attempts were made to distinguish different medicinal parts of P. hookeri.Results: Regression equation for 10 compounds showed good linear regression (R2 &gt; 0.9994). The relative standard deviations of precision, stability, repeatability and recovery were under 5 %. Compared with the aerial plant part, the root had significantly higher levels of sylvestroside I (p &lt; 0.01), cantleyoside (p &lt; 0.001), dipsanosides B (p &lt; 0.01) and dipsanosides A (p &lt; 0.01), but significantly lower levels of loganic acid (p &lt; 0.001), chlorogenic acid (p &lt; 0.01), and isochlorogenic acid (p &lt; 0.01). There were no significant differences between loganin, sweroside and isochlorogenic acid C.Conclusion: The described method is simple, accurate and reproducible, and can be used for the simultaneous determination of 10 major compounds of P. hookeri. The results demonstrate that there is variation in the chemical composition of the aerialpart and root of P. hookeri and that loganic acid and cantleyoside are the primary chemical biomarkers.Keywords: Tibetan medicine, Pterocephalus hookeri, Medicinal parts, Loganic acid and Cantleyoside, UPLC-PD

    Tetra­aqua­(nitrato-κ2 O,O′)bis­(pyridinium-4-carboxyl­ate-κO)europium(III) dinitrate

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    The asymmetric unit of the title compound, [Eu(NO3)(C6H5NO2)2(H2O)4](NO3)2, consists of one-half of the C 2 symmetric coordination cation and one nitrate anion. The eight-coordinated EuIII atom is in a distorted dodeca­hedral coordination environment. The coordination cations and nitrate anions are connected via O—H⋯O and N—H⋯O hydrogen bonds into a three-dimensional network
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