氨基乙酸

The process was methanolysis ed alkyl inino-acetic acid ester hydrogen chloride salt from methyl-cyanide.

研究了由乙腈为原料经烷基亚氨基醋酸酯盐酸盐醇解制备原乙酸三甲酯的工艺方法，对投料比、反应温度、反应时间及中和指示剂等工艺条件进行了研究，得出较优惠的工艺条件。

When the protoplast-derived calli were transferred into the MS solid medium added with 2.0mg/L benzylamino-purine and 0.4mg/L naphthaleneacetic acid and cultivated in the codition of low illumination, after which the adventitious shoots were induced, then we could obtain numerous plantlets and could transplant them survival to pots in the greenhouse.

当将原生质体分裂形成的愈伤组织转移到附加2.0mg/L6-苄氨基嘌呤和0.4mg/L萘乙酸的MS固体培养基上，并在低光照条件下培养后，从愈伤组织上分化出了不定芽，进而发展成小植株，并移栽成活。

The results showed that the reaction was greatly inhibited by its two products, where 6-APA is the uncompetitive inhibitor, and phenylacetic acid the competitive inhibitor.

结果表明，该反应受到产物6-氨基青霉烷酸(6-APA)的非竞争性抑制和苯乙酸的竞争性抑制。

Covering an area of 30 mu, the project is to produce graphitized carbon black, p-aminophenol and phenylacetic acid of 500 tons, 3,600 tons and 4,500 tons respectively after construction.

导电炭黑用途广泛，是电池电极的首选材料，目前国内尚需进口，国际上也很有市场；对氨基苯酚是国家一级大药厂的急需原料；苯乙酸是国家鼓励生产的新产品。

CH3OH has been designed, synthesized and characterized by X-ray diffraction analysis. In this dinuclear complex, it is worthy of notice that the source of tridentate chelate atoms (1N2O) of IDA is different from that of the reported complex.

合成过程中，我们还首次得到了与1，10-邻菲咯啉及亚氨基二乙酸络合的铜的不对称双核配合物晶体。

Methods: M-acetaminphen was used as an internal standard, and alkalinized samples of plasma were extracted with ethyl acetate.

以间乙酰氨基酚为内标，血浆样品经碱化后，用乙酸乙酯提取。

Methods: fudr was esterified with acetic anhydride in the presence of pyridine and 4 dimethylaminopyridine.

在吡啶和4 二甲氨基吡啶存在时，fudr与乙酸酐反应，制备氟尿苷二乙酸酯，并测定其核磁共振氢谱。rp hplc测定其在正辛醇和磷酸盐缓冲液中的分配系数及不同ph缓冲液和组织匀浆中的稳定性。

Objective To establish a HPLC method for the determination of aceclofenac in human plasma.Methods Acidified samples of plasma (500μL) were extracted with 4 mL of ethyl acetate. The organic phase was evaporated to dryness by nitrogen at 40℃ water bath. The residue was redissolved in mobile phase and then was determined.

醋氯芬酸是一种具有镇痛作用的非甾体类抗炎药物[1]，化学名为[邻-(2，6-二氯苯基)氨基]苯乙酰乙酸，l992年首先于西班牙上市，具有明显广泛的抗炎作用和强力的解热镇痛作用，其生物半衰期较双氯芬酸长，胃肠耐受性较双氯芬酸好，抗炎活性优于萘普生和保泰松[2]。

The results showed that Kaidimycin was chemically neutral, macrocylic polylactones, stable and liable to dissolve into water and pyridine, slight to dissolve into methanol, ethanol and N-butanol, difficult to dissolve into ethyl acetate, acetone, benzene and chloroform. Chemical reaction of functional group of Kaidimycin showed that it had glycoside, amino acid and aldehyde, no reducing sugar, polypeptide and phenol.

凯地菌素属中等极性的、中性抗生素，极性纸层析结果与多烯类抗生素的纸层析结果相似：易溶于水、吡啶，微溶于甲醇、乙醇、正丁醇，不溶于乙酸乙酯、丙酮、苯、三氯化碳；对高温、光照和紫外处理有很好的稳定性；官能团反应试验结果发现，凯地菌素可能含有糖苷键、氨基酸伯氨基和醛基，不含有还原糖、多肽和酚基，高锰酸钾、浓硫酸反应与多烯大环内酯类抗生素的特性相似；并且依据纯品，采用生物法和分光光度法对摇床发酵液进行了效价的测定。

The synthetic procedure consists of three steps: the preparation of magnetic silica microbeads by polymer templating method; coupling of iminodiacetic acid with a bifunctional silane agent 3-glycidoxypro-pyltrimethoxysilane; charging the magnetic support with Cu(superscript 2+) With bovine serum albumin as a model compound, the adsorption behavior of protein on the magnetic matrix was studied.

采用模板法制备的单分散磁性硅胶微球，经过表面修饰偶联上亚氨基二乙酸，与过渡金属离子Cu(上标 2+)螯合，制成一种新型的磁性固定化金属亲和纯化载体。

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。