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联羧基

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The present invention relates to a process for rapid solution synthesis of a peptide, the process comprising repetitive cycles of steps-: a coupling step, using an excess of an activated carboxylic component to acylate an amino component, a quenching step in which a scavenger is used to remove residual activated carboxylic functions, wherein the scavenger may also be used for deprotection of the growing peptide, one or more aqueous extractions and optionally, a separate deprotection step, followed by one or more aqueous extractions, characterised in that the process comprises at least one step, referred to as step, in which an amine or a thiol comprising a free anion or a latent anion is used as a scavenger of residual activated carboxylic functions.

本发明涉及快速溶液合成肽的方法,该方法包括步骤-的重复循环:偶联步骤,使用过量的活化羧基成分酰化氨基成分,淬灭步骤,在该步骤中使用清除剂除去残余的活化羧基官能团,其中该清除剂还可以用于使生长中的肽去保护,一或多个水抽提和任选地,独立的去保护步骤,之后进行一或多次水抽提,其特征在于该方法包括至少一个步骤,称作步骤,在该步骤中包含自由阴离子或潜阴离子的胺或硫醇用作残余活化羧基官能团的清除剂。

Appraised the clinical effect of the flavone of rhizome drynania on Senile Osteoporosis, according to the dynamic observation on integrative scores of lumbodorsal pain and lumbodynia,"VAS section grading method" on lumbodynia,"Barthel index rating method" on ADL, detected BMD on anterior-posterior position lumbar2~4 vertebra body and proximate of femur including neck/ward/troch, and determined the index of bone transition including BGP/PINP/ICTP through the radioimmunity method before and after treated half a year, then contrast intragroup and selfgroup. Depending on the standard of curative effect, contrast the difference of curative effect between two groups.

采用随机对照的方法,分为治疗组36例,对照组34例,依据对腰背痛及腰痛综合评分进行动态观察;依据"疼痛VAS线段分级法"对腰背痛(静止痛、翻身痛、久坐痛、起身痛、弯腰痛、步行痛、睡眠痛、叩击痛、压痛)进行量化动态观察;依据"Barthel指数评定法"对老年性骨质疏松症日常生活活动能力进行观察;采用双能X线骨密度仪对腰椎(L2-L4)、股骨近端各部位:股骨颈、股骨三角区、股骨粗隆进行骨密度定量检测;应用放射免疫法对骨转换指标进行测定,骨形成指标:骨钙素、Ⅰ型前胶原氨基端前肽;骨吸收指标:Ⅰ型胶原交联羧基末端肽等,评价骨碎补总黄酮治疗老年性骨质疏松症的临床效果。

Therefore esterification crosslinked reactionbetween polyearboxylic acid and wood can be quantitatively determined.According toexperiment results of stereoscopic configuration choices by crosslinking agents,crosslinkingreaction between model of reaction intermediate and wood,and the intermediate characteristic incrosslinking reaction,crosslinking reaction intermediate was proofed.We can infercrosslinking reactions between polycarboxylicacid and wood want through a mechanism of twosteps reaction process,the first cyclic anhydrides were formed as intermediates by dehydratingbetween hydroxyls in polycarboxylic acids,second esters were occurred by substitution reactionbetween wood hydroxyls and cyclic anhydrides.

从而可全面定量表征木材与多元羧酸类化合物的酯化交联反应;依据交联剂立体构型选择性、反应中间体模型物与木材的交联反应和交联反应中间体的波谱特征实验结果,证实了交联反应中间体,因此可以推测:多元羧酸类化合物与木材化学组分的交联反应是经历两步反应的机理,首先多元羧酸中相邻羧基的羟基之间脱水形成五元环酸酐中间体,然后木材的羟基与酸酐发生亲核取代反应形成酯。

The research results indicated that the first cross-linking between the HPAM and Cr3+ in ground condition was propitious to reduce leaking of blocking agent in oil layer, and the second crosslink action between acylamino of HPAM and organic phenolic aldehyde can form the high intensity gel and it can endure high temperature.

研究结果表明,HPAM羧基与Cr~(3+)离子在地面条件下的一次交联作用有利于减少堵剂在油层的漏失量,HPAM酰胺基与有机酚醛在地层条件下的二次交联作用,能够形成耐温高强度凝胶。

Ferrocenecarboxylic-ssdeoxyribonucleic acid probe was made by chemically bounding FCA to terminal 5'-amino of oligonucleotide in the presence of a water-soluble carbodiimide. The hybridization reaction was conducted by immersing the immobilized-ssDNA electrode in FCA-ssDNA probe solution.

在偶联活化剂碳二亚胺的存在下,通过羧基二茂铁上的羧基与DNA分子上的氨基共价键合,将FCA标记在氨基修饰的寡聚核苷酸片段上,制备成FCA-ssDNA探针。

Crystal by DTT into the protoxin with an end amino group; activation and derivation of abamectin to form abamectin-COONa with a carboxylic group; final bioconjugation by using amino-carboxylic conjugator EDC to achieve the substance combination of two biotoxins.

晶体进行酶解改造,形成带末端氨基的原毒素;将阿维菌素的羟基进行激活、衍生化,形成带羧基的阿维菌素衍生物(Abamectin-COONa);再利用氨基-羧基偶联剂进行两种生物毒素的生物耦合。

Appraised the clinical effect of the flavone of rhizome drynania on Senile Osteoporosis, according to the dynamic observation on integrative scores of lumbodorsal pain and lumbodynia,"VAS section grading method" on lumbodynia,"Barthel index rating method" on ADL, detected BMD on anterior-posterior position lumbar2~4 vertebra body and proximate of femur including neck/ward/troch, and determined the index of bone transition including BGP/PINP/ICTP through the radioimmunity method before and after treated half a year, then contrast intragroup and selfgroup. Depending on the standard of curative effect, contrast the difference of curative effect between two groups.

采用随机对照的方法,分为治疗组36例,对照组34例,依据对腰背痛及腰痛综合评分进行动态观察;依据&疼痛VAS线段分级法&对腰背痛(静止痛、翻身痛、久坐痛、起身痛、弯腰痛、步行痛、睡眠痛、叩击痛、压痛)进行量化动态观察;依据&Barthel指数评定法&对老年性骨质疏松症日常生活活动能力进行观察;采用双能X线骨密度仪对腰椎(L2-L4)、股骨近端各部位:股骨颈、股骨三角区、股骨粗隆进行骨密度定量检测;应用放射免疫法对骨转换指标进行测定,骨形成指标:骨钙素、Ⅰ型前胶原氨基端前肽;骨吸收指标:Ⅰ型胶原交联羧基末端肽等,评价骨碎补总黄酮治疗老年性骨质疏松症的临床效果。

The hydrophobic core serves as a reservoir for water-insoluble drugs.Hence,these nanoparticles can be used as carriers for hydrophobic drugs.For the synthesis of cholesterol-modified glycol chitosan conjugates,a carboxyl group was initially introduced to cholesterol molecule using succinic anhydride,and then covalently coupled with the primary amino group of glycol chitosan in the presence of 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide hydrochloride and N-hydroxyl succinimide.

本文采用二步反应将胆固醇接枝到乙二醇壳聚糖,首先将胆固醇进行羧基化,将胆固醇与琥珀酸酐反应生成胆固醇半琥珀酸酯,然后用1-乙基-3-(3-二甲基氨丙基)碳二亚胺盐酸盐与N-羟基琥珀酰亚胺作为偶联剂,将胆固醇半琥珀酸酯的羧基与乙二醇壳聚糖主链的氨基进行反应,得到胆固醇疏水改性乙二醇壳聚糖共聚物。

By synthesizing the hapten LBc starting from the metabolite of bifenthrin (2-methyl-3-phenylbenzyl alcohol), LBs (2-methyl[1,1-biphenyl]-3-ylmethyl 3-carboxyl-2,2-dimethylcyclopropane carboxylate and Lby (2-methyl[1,1-biphenyl]-3-ylcarboxylic acid , Three haptens were praparaed which were used in next step.

利用联苯菊酯的代谢物联苯醇合成了联苯菊酯的半抗原LBc(2-甲基-3-苯基苄基氧基羰基丙酸)、LBs(2-甲基-3-苯基苄基-3-羧基一2,2-二甲基环丙烷羧酸)和LBy(2-甲基-3-苯基苯甲酸)。

Multilayer latex particles with carboxylic polymer as core, polymer with low glass transition temperature and film-formable under room temperature as shell, and lightly crosslinked polymer as intermediate layer were prepared with unsaturated carboxylic monomers by multistage seed emulsion polymerization. Finally, the room-temperature-film-formable polymer particles with hollow structure were obtained via the alkali treatment to the multilayer latex particles.

采用羧基单体进行多阶段的种于乳液聚合,制备了内核为带羧基的聚合物、最外层为易成膜的低玻璃化温度聚合物、中间为轻度交联中间隔离层的多层核壳结构乳胶粒,最后通过碱处理制成了具有室温成膜性的中空结构聚合物微粒。

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