硫酰

Nine seasickness adaptive proteins were identified by PMF: peroxiredoxinⅠ, peroxiredoxinⅡ, light molecular-weight neurofilament, ubiquitin carboxyl-terminal hydrolase PGP9.5, and glutamine synthetase were highly expressed; carbonic anhydraseⅡ, triosephosphate isomeraseⅠ, phosphoglycerate mutase isozyme B and mitochondrial voltage dependent anion channel were lowly expressed.

获得了9个晕船适应相关蛋白质：硫氧还蛋白过氧化物酶Ⅰ、硫氧还蛋白过氧化物酶Ⅱ、低分子量神经丝蛋白、泛素羧基末端水解酶PGP9.5和谷氨酰胺合成酶上调；碳酸酐酶Ⅱ、磷酸丙糖异构酶Ⅰ、磷酸甘油酸变位酶B和线粒体电压依赖型阴离子通道下调。

Cytotoxic effect was demonstrated with nitrogen mustard, nitromin, sarcolysin, thio-TEPA and myleran at concentrations of 7, 10, 25, 35, 100, and 100μg/ml respectively.

氮芥及氧化氮芥在7—10微克/毫升，溶肉瘤素和新恩必恨于25—35微克/毫升，三乙酰硫代磷酰胺和丁二醇二甲磺酸酯在100微克/毫升，都出現了显著的細胞毒作用，使細胞很快死亡溶解；但6-巯基嘌吟和氨基喋吟未表現作用。

Benzyloxy benzoyldimethylsulfoxide was prepared by the reaction of ethyl 4-benzyloxybenzoate and dimethyl sulfoxide in the presence of sodium hydride, followed by Pummerer reaction with concentrated hydrochloric acid to afford eo-hydroxy-co-thio-methyl-(4/-benzyloxy) acetophenone, which reacted with urea, thiosemicarbazide, semicarbazide hydrochloride and o-phenylenediamine to give imidazolidine-2,4-dione, l,2,4-triazine-3- one and quinoxaline derivatives, respectively.

本文用4-苄氧基苯甲酸乙酯和二甲亚砜为原料，在氢化钠存在下反应，合成了(4′-苄氧基)-苯甲酰基-二甲亚砜。研究了该亚砜在浓盐酸的存在下发生的Pummerer重排反应，用重排产物ω-羟基-ω-甲硫基-(4′-苄氧基)-苯乙酮分别与尿素、氨基脲、氨基硫脲和邻苯二胺反应合成了2，4-咪唑啉-二酮、1，2，4-三嗪-3-酮、喹喔啉等含氮杂环化合物。

METHODS: A series of N-octyl-N'-succinyl chitosan labeled with fluorescein, were incubated with HepG2 liver cancer cells, K562 leukemia cells, A549 human lung cancer cells, and BGC cancer cells respectively and followed by using flow cytometry and enzyme-linked immunosorbent assay to assess the affinity and inhibition of N-octyl-N'-succinyl chitosan for the four kinds of tumor cells already mentioned.

用异硫氰酸荧光素对N-正辛基－N'-琥珀酰基壳聚糖进行标记，再分别与人肝癌细胞(HepG2)、人白血病细胞(K562)、人非小细胞肺癌细胞(A549)及人胃癌细胞共培养，通过流式细胞仪及酶联免疫检测仪测定N-正辛基－N'-琥珀酰基壳聚糖对肿瘤细胞的亲和性及抑制力。

The analysis of SAR reveals that the activities of target compounds are closely associated with the electron-withdrawing substituents at the para position of 1-aryl-1, 2, 4 -triazoles as well as with the substituents such as sulfonyl and methylthio groups at the 3 position of 1, 2, 4 -triazoles; And the introduction of sulfamoyl moiety at the para position of 5-aryl-1,2,4-triazoles also has significant influence on the anti-inflammatory activity of these compounds.

构效关系分析发现，在三唑环1位芳基的对位引入F、Cl、Br吸电子基团以及3位引入磺酰基和甲硫基，对抗炎活性有重要的意义；在三唑环5位芳基的对位引入氨磺酰基，对抗炎活性有较大影响。

Methacryloyloxydecyl-2-thiouracil-5-carboxylate was synthesized from the reaction of thiouracil with diethyl ethoxymethylene malonate and ω-hydroxy-decyl-methacrylate.

以硫脲、乙氧基次甲基丙二酸二乙酯和甲基丙烯酸ω-羟癸酯为主要原料合成了一种新的粘接性单体10-甲基丙烯酰氧癸基－2-硫脲嘧啶－5-羧酸酯。

There was great effect of the quantity of ureide in every organic by sulfur.

东农42施硫肥处理对地上部器官酰脲分布产生很大的影响，但各部分硫效反应时期是不同的。

By the reactions ofα-acylamino ketene--acetals and oxalyl chloride, a serie of pyrrolidinetriones were prepared.

通过α-酰胺基二硫缩烯酮和草酰氯的反应，成功制备了一系列吡咯烷酮类化合物。

A series of 2-acetylformanilides were prepared,followed by thiolation with Lowesson reagent to afford 2-acetylthioformanilides,which further reacted with Mn3·2H2O in glacial acetic acid under microwave irradiation to afford 2-acetyl benzothiazole s.

合成了一系列的硫代酰胺，研究了它们在微波辐射醋酸锰作用下发生氧化自由基环化反应，成功地合成了一系列2-乙酰基苯并噻唑衍生物，其结构经红外光谱、核磁共振谱和质谱得到了证实

Methods: Uses carbon tetrachloride (CC14) 2ml/kg, thioacetamide 200mg/kg, the abdominal cavity to inject separately, Establish model which the rat acute liver damages; Guarantees the liver profit stomach mixture, the polyene phosphatide acid radical choline capsule, the glycyrrhizic acid diamidogen capsule fills the stomach.

分别用四氯化碳(CC14)2mL/kg，硫代乙酰胺200mg/kg，腹腔注射，建立大鼠急性肝损伤的模型；保肝益胃合剂，多烯磷脂酰胆碱胶囊，甘草酸二胺胶囊灌胃治疗。

They weren't aggressive, but I yelled and threw a rock in their direction to get them off the trail and away from me, just in case.

他们没有侵略性，但我大喊，并在他们的方向扔石头让他们过的线索，远离我，以防万一。

In slot 2 in your bag put wrapping paper, quantity does not matter in this case.

在你的书包里槽2把包装纸、数量无关紧要。