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N,N-dimethyl-N'-(2-trifluorometyl-1-pentafluoroethyl) perfluoro propenyl propane diamine and N,N-dimethyl N'-(2-trifluorometyl-1-pentafluoroethyl) perfluoro propene propane diamine were prepared by the reaction of hexafluoropropene dimer and N,N-dimethyl propanediamine in the molar ratio 1:1.0 at about 35℃for 8h, and the structures of I were identified by IR and NMR spectra.

本文以六氟丙烯二聚体和N,N-二甲基丙二胺为主要原料合成了两种含氟中间体叔胺——N,N-二甲基-N'-(2-三氟甲基-1-五氟乙基)全氟丙烯基丙二胺和N,N-二甲基-N'-(2-三氟甲基-1-五氟乙基)全氟烯丙基丙二胺,用薄层色谱和柱色谱等方法对产品进行分离提纯,并运用红外光谱和核磁共振等分析手段对其结构进行了表征。

The study on acetoin crystallization dimer showed that the yield of acetoin-dimer was affected by the optical rotation of acetoin.

对乙偶姻二聚体结晶的研究表明,乙偶姻的旋光值对二聚体的结晶得率影响很大,旋光值越接近于零,结晶得率越高。

Cyclopentadiene monomer is not stable and undergoes spontaneous Diels-Alder addition to produce the dimer and higher polymers.

环茂二烯单体是不稳定的,它会自发进行Diels-Alder加成反应,产生二聚体和更高的多聚体。

DFA-PEG polyester was synthesized with DFA and PEG 400 at first, and then bysulfating DFA-PEG polyester with NH_2SO_3H or terminating DFA-EG polyester withrosin acid, two derivant, these are sulfated DFA-PEG polyester and terminateDFA-PEG polyester, were synthesized. The reaction conditions of synthesis wereoptimized by orthogonal experiments.The molecular weight of product was analyzed by GPC.

5以二聚脂肪酸和聚乙二醇400为原料,首先合成了DFA-PEG聚酯,再以DFA-PEG聚酯为衍生体,硫酸化或用松香封端,合成了两种DFA-PEG聚酯衍生物——DFA-PEG聚酯硫酸酯盐和松香酸封端DFA-PEG聚酯,通过正交试验,对合成的条件进行了优化。

Access to the catalytic center and an unusual switch I movement in the dimeric structure support this finding.

二聚体中催化中心的入口和一种不寻常的开关运动支持了这一猜想,即易位子复合物之间的相互作用或蛋白质前体的潜在结合位点都是由这种二聚体的结构特点决定的。

The invention relates to a method for preparing dimeric acid methyl ester and dimer acid thereof.

本发明是一种制备二聚酸甲酯及其二聚酸的制备方法,以不饱和脂肪酸甲酯含量较高的混合脂肪酸甲酯或混合脂肪酸为原料,浓硫酸为助催化剂,无水氯化铝或无水氯化锌为催化剂,采用两步催化法进行二聚化反应。

In present study, we demonstrated that μ opioid receptor and D1 dopamine receptor could form heteromeric complexes in membranes preparation from HEK293T cells transiently cotransfected with both receptors and from mice striatum.

在本工作中,我们通过免疫共沉淀和BRET法证明,HEK293T细胞上瞬时表达的μ阿片受体和D1多巴胺受体能形成异源二聚体,并证实μ阿片受体和D1多巴胺受体异源二聚体存在于小鼠纹状体中。

In addition, our data indicated that the conformation of NR1 subunit homodimers was affected by the partner NR2 subunits during the formation of heteromeric receptor complexes, which might underlie the mechanism by which NR2 subunits modify NMDA receptor function. We also found that in the endoplasmic reticulum, even the whole extracellular N-terminal domain was truncated, the NR subunit could form homomers or heteromers with each other in HEK293 cells, which indicate that the NT is not the crucial element for the receptor assembly.

同时,通过推算FRmax,我们发现NR亚单位同二聚体的N端构象在形成功能性受体的前后是发生变化的,特别是对于NR1a亚单位,其同二聚体的N端构象会因与其配对的NR2亚单位的不同而发生不同的改变。

Erve growth factor combined with its receptor, activated Ras - MAP kinase , mitogen - activated protein kinase kinase is the important regulating factor that make IkB kinase, IKK, phosphated, IkB kinase make the IκBα:(the subunit of NF -κB ) phosphated, the phosphated IkBα degraded, and p65 - p50 heterodimer can be formed, then the heterodimer translocated to nucleus and combined with the promoter domain or other consensus sequence.

GF与其受体相结合,最后可以激活Ras-有丝分裂激活的蛋白激酶途径,有丝分裂激活的蛋白酶激酶(MEKK1)是IγB激酶发生磷酸化的重要调节因子,IKK使NF-κB的亚单位IKBα发生磷酸化,磷酸化的IKBα发生降解,而最后留下p65-p50二聚体,该二聚体然后转位到细胞核内与κB基因的增强子区域或与他的顺式作用序列结合。

The result expressed that under the concentration of 0.2mg/mL, the 6 compounds are all active to Sarcina lutea, ME-1, MT-6, MT-land MT-7 are active to Bacillus megaterium, to Escherichia coli, only MT-2 is active. The dimeric natural products are intensively existed in botany, most of them have the obvious biological activities. They have been concentrated on in recent years, and they are one of the compounds to which are enjoyed great popularity in natural product.

结果表明,在浓度为0.2mg/mL的条件下,六种化合物对藤黄八叠球菌均具有明显抑制作用,ME-1、MT-6、MT-1、MT-7对巨大芽孢杆菌有抑制作用,MT-2对大肠杆菌有抑制作用,对绿脓杆菌和枯草芽孢杆菌六种成分均无抑制作用;二聚体化合物在植物界广泛存在,多数二聚体天然产物具有显著的生物活性,引起人们的重视,是天然产物化学界研究的热门化合物之一。

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