琥珀酰亚胺

通过红外光谱（IR）和核磁共振光谱（NMR）可以发现PAL具有独特的琥珀酰亚胺和聚乳酸分枝体系结构。

The unique branched architecture comprising succinimide units and lactic acid units was confirmed by infrared spectrum ( IR ) and nuclear magnetic resonance spectrum ( NMR ) .

N-（1-萘基）-琥珀酰亚胺化合物晶体结构的理论预测

Theoretical Prediction of Crystal Structure of N - ( 1-naphthyl ) Succinimide Compound

N羟基琥珀酰亚胺活化酯用于肽合成；

N hydroxysuccinimide activated ester was used in peptide synthesis ;

方法通过蛋白交联固化及N羟基琥珀酰亚胺基3（2吡基二硫）丙酸脂（SPDP）交联的方法制备蛋白免疫微球。

Methods Immuno-nanospheres were prepared by methods of protein cross-linking solidify and SPDP cross-linking .

将NHS（N羟基琥珀酰亚胺）酯功能基团引入高分子载体上，合成了几种聚合物的NHS酯。

N Hydroxysuccinimide functional group was introduced into polymer carrier to synthesize a couple of polymer NHS esters .

活化能数据为：DL-聚琥珀酰亚胺与NaOH反应的活化能为75.1kJ／mol。

The active energy of the reaction between poly ( succinimide ) and NaOH was 75.1 kJ / mol.

方法底物制备采用N-羟基琥珀酰亚胺活化酯合成多肽法；建立分光光度法测定ACE的活性。

Methods The substrate was prepared by the use of N-hydroxysuccinimide ester in peptide synthesis , and serum ACE was determined by spectrophotometric assay using substrate .

第一章是N-溴代琥珀酰亚胺（NBS）化学发光体系的应用，全章分为五节。

Chapter 1 describes the application of N-bromosuccinimide ( NBS ) chemiluminescence system , and five sections are contained in this chapter .

在碱性介质中，硫酸小诺霉素能被N溴代琥珀酰亚胺（NBS）氧化，在荧光素的增敏作用下，产生化学发光。

A new method for the determination of micronomicin with flow injection chemiluminescence was described . It was based on the chemiluminescence during the oxidation of micronomicin by N-bromosuccinimide ( NBS ) in alkaline medium in the presence of fluorescein as energy transfer .

N-溴代琥珀酰亚胺-荧光素体系流动注射能量转移化学发光法测定妥布霉素

Flow Injection Energy Transfer Chemiluminescence Analysis of Tobramycin Based on N-Bromosuccinimide-Fluorescein System

N-溴代琥珀酰亚胺体系流动注射化学发光测定抗生素类药物

Flow Injection Chemiluminescence Analysis of Antibiotics Based on N-bromosuccinimide

N-（1-萘基）琥珀酰亚胺分子间相互作用的计算机模拟

Computer Simulation of Intermolecular Interaction of N - ( 1-naphthyl ) - succinimide

室温下N-羟基琥珀酰亚胺活化酯法合成吡咯-2,5-二乙酰胺

Synthesis of a Pyrrole-2,5-Diacetamide Derivative at Room Temperature Using the Activated Ester of N-Hydroxysuccinimide

建立了一种利用琥珀酰亚胺代谢从延胡索酸生产丙酮酸的新工艺。

A novel pathway for pyruvate production via fumarate was found in succinimide-assimilating microorganisms .

N-（1-萘基）-琥珀酰亚胺光谱性质与构象的计算机模拟

Computer simulation on the spectroscopic properties and conformation of n - ( 1-naphthyl ) succinimide

酶经N-溴代琥珀酰亚胺作用后活力逐渐丧失。

The reaction of the enzyme with N-bromsucciniamide also led to a gradual loss of activity .

硫辛酸N-琥珀酰亚胺基酯的合成研究

Synthesis of Thioctic N-Hydroxysuccinimide Esters

聚乙二醇琥珀酰亚胺酯修饰牛血红蛋白作为红细胞代用品的条件研究

Research on Prerequisite for Using Bovine Hemoglobin Modified by Polyethylene Glycol as a Red Blood Cell Substitute

光诱导的5,5-二取代二氢吡咯类硝酮与N-溴代琥珀酰亚胺的反应

Photoinduced reactions of 5 , 5 - disubstituted - 1 - pyrroline n - oxides with N - bromosuccinimide

的胺，用N-羟基琥珀酰亚胺（HOSu）（2equiv.）游离羟基及表面活性剂对乙草胺光解的影响

And a coupling agent , DCC ( 2 equiv. ) Effect of hydroxide radical and surfactant on photodegradation of acetochlor

几种酰亚胺和酰胺的N-烷基化反应&邻苯二甲酰亚胺、琥珀酰亚胺和乙酰苯胺在相转移条件下N-烷基化反应的研究

N-Alkylation of Several Imides and Amides & A Study of the N-Alkylation of Phthalimide , Succinimide and Acetanilide Under Phase-Transfer Conditions

利用两种方法合成了硫辛酸N-琥珀酰亚胺基酯，并用核磁和质谱进行了结构表征。

Synthesis of thioctic N-hydroxysuccinimide esters by two kind of way in this paper , and structure is showed by MS and H-NMR .

研究了以顺丁烯二酸酐和浓氨水为原料合成了聚天冬氨酸的聚合反应工艺。通过控制工艺条件，直接液相聚合得到了聚琥珀酰亚胺。

Poly ( succinimide ) is synthesized by the directly reaction of maleic anhydride and ammonia in water by controlling the process conditions .

高效液相色谱-荧光分析法测定人体尿液中的蝶呤-6-羧酸羧基荧光素琥珀酰亚胺酯标记肿瘤细胞及其在细胞毒检测中的价值

Determination of Pterin-6-carboxylic Acid in Human Urine by HPLC with Fluorescence Detection Fluorescent dye of CFSE used for labeling tumor cells and determining cytotoxicity

方法以马来酸酐为原料，经加成，环化，还原、环合4步反应得到N-羟基琥珀酰亚胺磺酸钠，N-羟基琥珀酰亚胺磺酸钠与相应的二羧酸反应得到目标产物。

METHODS Sulfo-N-hydroxy succinimide sodium was prepared from maleic anhydride , via four steps , including addition , cyclization , reduction and cyclizative condensation . The target compound was obtained by sulfo-N-hydroxy succinimide sodium reacting with corresponding dicarboxylic acid .