Aim : To have a preliminary evaluation of 1 H - MRS application in ALS patients.
目的: 探讨~1H-MRS在ALS患者 的临床应用价值.
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The reaction 5 - amino - lH - pyrazole with 2,4 - dichlorophenoxy acetyl chloride was studied.
2.研究了 5- 氨基 -1H- 吡唑与2,4-二氯苯氧乙酰氯反应的选择性和反应性能.
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AIM To study the antioxidant activity of 2 - ethyl - 3 - hydroxy - 6 - phenylthio - 4 ( 1 H ) - pyridone ( HPP ).
目的 研究2乙基3 羟基 6苯硫基4 ( 1H ) 吡啶酮 ( HPP ) 的抗氧化作用.
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The structure was verified by 1 H - NMR, GPC and end group titration techniques.
通过核磁共振氢谱(1H-NMR) 、 凝胶渗透色谱(GPC) 、端羟基滴定等方法,研究了所合成的三嵌段共聚物的结构.
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Ziprasidone hydrochloride and its intermediate chemical structure by 1 H - NMR , MS, IR confirmed.
盐酸齐拉西酮及其中间体的化学结构经 1H-NMR 、 MS 、 IR确证.
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Most of the ADR occurred 1 h after administration.
不良反应均发生在用药1h后.
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One hour after sugar tolerance , the level of BG, Ins , cp and SS was increased markably, while Gluc was decreased.
糖负荷1h后血糖 、 胰岛素 、 C肽 和生长抑素水平上升, 胰高血糖素水平下降.
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RESULTS The degree of quaternization of TMC 40 and TMC 60 were 38.8 % and 67.2 % , respectively.
结果经1H-NMR确定 合成得到的TMC40,TMC60季铵化程度分别为38.8%和67.2%.
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Results Eighteen titled compounds were synthesized, their structure were confirmed by 1 H - NMR and MS analysis.
结果共得到18个目标化合物, 经 1H-NMR 、MS确证其结构.
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By means of clement analysis, IR, MS, H - NMR the constitution of 5 compounds were proved.
它们的结构由元素分析 、 IR 、 MS和~1H-NMR得到确证.
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The structures of the compounds are characterized by IR, 1 H - NMR , 13 C - NMR , 31 P - NMR , MS and HRMS.
所合成的化合物结构经IR 、 1H-NMR 、 13C-NMR 、 31P-NMR 、 MS和 高分辨质谱(HRMS) 分析确证.
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In group, patients showed elevated total CTT ( mean , 175.1 h ) and rectosigmoidal CTT [ mean , 115.8 h ( 66.1 % ) ].
第3组, 平均总CTT ( 175.1h ) 和直肠乙状结肠CTT [ 115.8h ( 66.1% ) ] 均明显延长.
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Result: When Scutellaria baicalensis was vapoured for an hour , it turned soft and bright yellow.
结果: 黄芩蒸1h软化切片,色黄鲜艳,黄芩素含量较高,质量较好, 与冷浸24h切片比较,黄芩素含量平均高22.9%.
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ATP decreased moderately at 1 hour, and remain the similar level until 12 hour.
1h后 血肿周围组织ATP含量 呈中度下降,但无统计学意义.1h至 12h间 ATP含量 在略有波动,在12h后再次下降, 至24h达最低点,有统计学意义.
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