硝酐

Methods The antianaphylaxis activities of myricetin was measured by passive cutaneous anaphylaxis, dextran-induced itch and DNCB-induced delayed type hypersensitivity in mice,respectively.

采用小鼠同种、异种被动皮肤过敏反应、右旋糖酐致小鼠全身瘙痒反应和2，4-二硝基氯苯所致小鼠耳廓皮肤迟发型超敏反应实验，探讨杨梅素的抗过敏作用。

Methods The activity of urine NAG isoenzyme, NAG/Cr and blood NAG isoenzyme in 47 patients with acute CVD (15 patients with brain hemorrhage and 32 patients with brain infarction) were examined by p-nitrobenzene chronometry.

采用对硝基酚比色法，分别测定了47例急性脑血管疾病患者（其中脑出血15例，脑梗死32例）的尿液NAG同工酶谱、尿NAG与尿肌酐的比值、血清NAG活力。

Objective To evaluate relationship between urine NAG isoenzyme and acute cerebrovascular disease. Methods The activity of urine NAG isoenzyme, NAG/Cr and blood NAG isoenzyme in 47 patients with acute CVD (15 patients with brain hemorrhage and 32 patients with brain infarction) were examined by p-nitrobenzene chronometry.

目的 探讨尿液N-乙酰-β-D-氨基葡萄糖苷同工酶与急性脑血管病的关系方法采用对硝基酚比色法，分别测定了47例急性脑血管疾病患者（其中脑出血15例，脑梗死32例）的尿液NAG同工酶谱、尿NAG与尿肌酐的比值、血清NAG活力。

Chemical corporations within this region may provide matching chemical products and raw materials such as citric acid, starch sugar, L-lactic acid, nitrochlorobenzene, paranitrophenol sodium salt sodium para-nitro phenolate, pphenylenediamine , sodiumhydroxide, benzene anhydride, carbonic acid propylene grease, polyacrylamide ,2.4- dinitrochlorobenzene, 2.4- dinitrosixchlorin, and sodium cyanide.

区内化工企业可配套提供柠檬酸、淀粉糖、 L —乳酸、硝基氯苯、对硝基酚钠、对苯二胺、烧碱、苯酐、碳酸丙烯脂、聚丙烯酰胺、2.4—二硝基氯化苯、2.4—二硝基6氯、氰化钠等化工产品或原料。

The result fights allergic experiment to show, dispel the wind stops land of can different level restrains urticant Ding allergy of akin and passive skin mixes the bandicoot that antiserum causes 2, the sex of small rat late hair of chloric benzene be caused by exceeds 2 nitro- of 4- quick the thymus index that reaction; still can increase small rat when dosage greatly and lienal index; stop urticant experiment shows, dispel the wind stops urticant Ding can reduce the time of fit of small rat itching with dextrose lead anhydride and itching duration apparently, can increase Guinea pig to be able to bear or endure those who suffer phosphoric acid histamine send urticant threshold.

结果抗过敏试验显示，祛风止痒酊能不同程度地抑制抗血清诱发的大鼠同种被动皮肤过敏和2，4-二硝基氯苯所致的小鼠迟发性超敏反应；大剂量时还可增加小鼠的胸腺指数及脾指数；止痒试验显示，祛风止痒酊能明显降低右旋糖酐诱导的小鼠搔痒发作次数及搔痒持续时间，并能增加豚鼠耐受磷酸组胺的致痒阈。

The nitration of toluene was carried out in the presence of acetic anhydride with CCl4 as solvent, 95% nitric acid as nitrating reagent, and niobic acid calcinated at 300℃ for 3 h as catalyst for 60 min at 40℃.

实验结果表明，当反应温度为40℃，反应时间为60min时，以CCl4为溶剂，以质量分数为95%的硝酸为硝化剂，在醋酐存在条件下，以经300℃焙烧3h后的铌酸作为催化剂，甲苯硝化产物中异构体的邻对比达1.26，较硝硫混酸的1.67显著降低，产物得率达99.3%。

Urinary NAG activities were measured by nitrophenol colorimetric analysis technique.

用生化法测定血肌酐，用硝基苯酚比色法测定尿NAG。

The results show high selectivity when the temperature is controlled at 50 CC , and the nitrated reaction time is 90 mm, toluene is nitrated by using 95% nitric acid as nitrating reagent at the presence of acetic anhydride, 1.0g silicotungstic acid catalyst is calcinated at 300℃ for 1.5h. The o/p (ratio of ortho to paro isomer of toluene nitration) ratio is 0.89 in product distribution of toluene nitration, lower than 1.67 using sulfonitric acid as catalyst. The yield of products is 91.6%.

结果表明，在醋酐存在条件下，以CCl4为溶剂，以质量分数为95%的硝酸为硝化剂，反应温度控制在50℃，反应60 min， 1.0g经300℃焙烧1.5h后的硅钨酸催化剂，对甲苯表现出强的区城选择性，甲苯硝化产物o/p值（甲苯硝化产物邻位和对位异构体的质量比）达0.89，较硝硫混酸的1.67显著降低，产物收率达到91.6%。

Methods: 2ethyl aniline was used as starting material of the synthesis and was processed by acetic anhydride acylation, strong nitric acid nitraction at low temperature, and desacyl synthesis to produce 2ethyl5nitro aniline. The product was then synthesized to 3methyl6nitro1Hindazole by using ringclosing reaction in the presence of NaNO2, and then ethylated to obtain 2,3diethyl6 nitro2Hindazole. The latter compound was then reduced by SnCl2/Hcl to get target compound 2,3diethyl6nitro2Hindazole.

以2乙基苯胺为原料经醋酐酰化、浓硝酸低温硝化及去酰基保护合成2乙基5硝基苯胺，后用亚硝酸钠关环得3甲基6硝基1H吲唑，经硫酸二甲酯甲基化得2，3二甲基6硝基2H吲唑，最后用氯化亚锡将其还原得到目标产物，通过1H NMR确定结构与目标产物一致。

Methods: 2-ethyl aniline was used as starting material of the synthesis and was processed by acetic anhydride acylation, strong nitric acid nitraction at low temperature, and desacyl synthesis to produce 2-ethyl-5-nitro aniline. The product was then synthesized to 3-methyl-6-nitro-lH-indazole by using ring-closing reaction in the presence of NaNO2, and then ethylated to obtain 2, 3-diethyl-6- nitro-2H-indazole. The latter compound was then reduced by SnC12/Hcl to get target compound 2, 3-diethyl-6-nitro-2H-indazole.

以2-乙基苯胺为原料经醋酐酰化、浓硝酸低温硝化及去酰基保护合成2-乙基－5-硝基苯胺，后用亚硝酸钠关环得3-甲基－6-硝基－1H-吲唑，经硫酸二甲酯甲基化得2，3-二甲基－6-硝基－2H-吲唑，最后用氯化亚锡将其还原得到目标产物，通过1HNMR确定结构与目标产物一致。

Plunder melds and run with this jewel!

掠夺melds和运行与此宝石！

My dream is to be a crazy growing tree and extend at the edge between the city and the forest.

此刻，也许正是在通往天国的路上，我体验着这白色的晕旋。