酰氨基

Analgesics commonly found in OTC cold medications are acetaminophen,ibuprofen,and acetylsalicylic acid.

常见的止痛药，发现在场外交易冷战药物对乙酰氨基酚，布洛芬，乙酰水杨酸。

Here we found the optimum situation to determine LAP: the concentration of Tris-HCl is 125 mmol L^(-1) and the optimum pH is 7.2, temperature is 37℃, under this condition, Michaelis constant is 0.15 mmolL^(-1), ground substance concentration is 6.0 mmol L^(-1), with 157 health people serum samples (81 from male, 76 from female),x± s=35.7 UL^(-1)±8.2 UL^(-1), we established the method and reference value for clinical application and automatic analysis.

测定亮氨酰氨基肽酶的最适条件：选用浓度为125mmolL^(-1)的Tris-Hcl缓冲液，最适pH为7.2，温度取37℃，得出在此实验条件下的米氏常数Km为0.15mmolL^(1)，亮氨酰对硝基苯胺浓度取6.0mmolL^(-1)，取健康体检者血清157例（男81例，女76例），测得x±s为35.7UL^(-1)+8.2UL^(-1)，建立了适合于临床应用及有动生化分析仪的方法和参考值。

ABSTRACT Immobilized penicillin acylase (from E.coli) was used to catalyze 7 phenylacetamido 3 E propenyl cephalosporanic acid hydrolyzation into 7 amino 3 E propenyl cephalosporanic acid. Then, trans APRA was acylated with hydroxyethyl ester of 4 hydroxy D phenylglycine to obtain trans cefprozil.

以7 苯乙酰氨基 3 E 丙烯基 3 头孢菌素 4 羧酸为原料，在青霉素酰化酶作用下，首先酶法水解得到3 E 丙烯基 3 头孢菌素 4 羧酸，过滤固相酶，滤液调pH分离得到反式APRA固体；在青霉素酰化酶作用下，反式APRA再与对羟基苯甘氨酸乙二醇酯缩合，得到反式头孢丙烯；酶法合成所得的产品与进口反式头孢丙烯对照品一致。

Amino to acetyl phenol, in have technology of two kinds of production domestic and internationally, acetic anhydride craft of the United States, acyl changes temperature to have 75 ℃ only, acyl changes mother liquor not apply mechanically, deputy reaction is little, of production thick tasting is kind of white almost, purificatory craft is very simple, activated carbon dosage only 2~3%, the Kun that its product does not have glow material almost in different third alcohol inferior the sealed impurity of amine impurity and minim, settleclear lightness it may not be a bad idea, the product quality that acetic anhydride craft produces is good, but close rate low, cost is high.

对乙酰氨基酚，在国内外有两种生产工艺，美国的醋酐工艺，酰化温度只有75℃，酰化母液不套用，副反应少，生产的粗品几乎是类白色，精制工艺就非常简单，活性炭用量仅2~3%，其产品在异丙醇中几乎无红光物质的醌亚胺杂质及微量的未知杂质，澄明度也好，醋酐工艺生产的产品质量好，但收率低、成本高。

In order to improve their water solubility, 4"-fatty amido-3"-sodium carboxylate azobenzene-4-sodium sulfonates were synthesized. They are azo compounds with two hydrophilic groups of carboxyl and sulfonyl. They decrease the surface tension in dilute solution slowly, and show some surfactivity, but are not surfactants. The probable reason is their relative strong hydrophile. Furthermore, their colors are not fresh and far from our destination.

为了改善其水溶性，改用对氨基苯甲酸为原料合成了4′-脂肪酰氨基-3′-羧酸钠偶氮苯-4-磺酸钠盐，以偶氮结构为主的亲水基团上连有羧酸基和磺酸基两个亲水性较强的基团，但可能由于其亲水性太强，在稀溶液中只能缓慢地降低溶液的表面张力，具有一定的表面活性，但不是表面活性剂，而且颜色不鲜艳，距离我们的目标较远。

A fluorescent boronic acid, dapoxylTM 3-sulfonamidophenylboronic acid was first used for the determination of glucose.

荧光染料(3-〔5-（4-二甲氨基苯基)-4，5-二氢唑-2-苯磺酰氨基〕苯硼酸被首次应用于体液中葡萄糖的直接测定。

A key intermediate of abacavir, named N-(2-amino-4,6-dichloro-5-pyrimidinyl) formamide was synthesized from diethyl malonate and guanidine hydrochloride. This method suits to industry for large scale. The materials are easy to get and very cheap.

2-氨基-4，6-二氯-5-甲酰氨基嘧啶是合成阿巴卡韦的关键中间体，本文拟以丙二酸二乙酯和盐酸胍为起始原料合成这一关键中间体，具有原料来源广，适合大规模生产等优点。

On the basis of these principles and requirements,in this paper,a new modifier has been synthesized from pyromellitic dianhydride and thiosemicarbazide by the nucleophilic addition of anhydride,the cyclization of acyl thiosemicarbazide in alkaline solution,and the N-hydroxymethylation of the triazole-thione.

本文根据这一思路，以均苯四甲酸二酐和氨基硫脲为起始原料，通过酸酐的亲核加成反应、酰氨基硫脲的碱性环化反应、三唑硫酮环的N-羟甲基化反应合成出了一种新的N-羟甲基三唑硫酮酸改性剂。

Synthesizc 2-methyl-5-acetamino benzene sulfochloride using p-toluidine primer reactant by aceylation and chlorosulfonation.

以对甲基苯胺为起始原料，通过乙酰化和氯磺化反应合成2-甲基－5-乙酰氨基苯磺酰氯。

A new tripodal aryl amide type ligand,1,1,1-tris{[(2′-benzylaminoformyl)phenoxyl]methyl}-p-toluene sulfonyl aminomethane,and its Eu(NO_3)_3,Tb(NO_3)_3 complexes have been synthesized.

合成了一个新的三足芳香酰胺型有机配体1，1，1-三[(2′-甲酰苄胺苯氧)甲基]对甲苯磺酰氨基甲烷，及其Eu(NO3)3和Tb(NO3)3的配合物，并通过元素分析、红外光谱、核磁共振氢谱和摩尔电导率进行了表征。

The split between the two groups can hardly be papered over.

这两个团体间的分歧难以掩饰。

This approach not only encourages a greater number of responses, but minimizes the likelihood of stale groupthink.

这种做法不仅鼓励了更多的反应，而且减少跟风的可能性。