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analogues相关的网络例句

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与 analogues 相关的网络例句 [注:此内容来源于网络,仅供参考]

The problem of incongruous counterparts can be raised even for objects in one-dimensional space if those objects are assumed to have non-topological but local properties such as color, or if objects may be non-connected, i.e."not in one piece." It is less clear whether the problems about time that have no spatial analogues are connected with the one-dimensionality of time.

这类问题(——the "problem of incongruous counterparts『类比会带来不协调的问题』"),即使处在一维空间中的客体,也是可以提出的,如果这些客体假设了拥有非拓扑但局部的属性,例如颜色,或如果客体可以是non-connected『非拼接的』,即"not in one piece『不是一个整块』")不太清楚,时间关联于一维的那些问题,是否有空间的类似问题。

In order to study its structure function relation, seven peptide segments and five analogues were designed and synthesized.

为进一步研究其结构与活性的关系,设计并合成了它的7个肽片段和5个类似物。

Methods: In this paper, a quinazoline purine analogues for the parent nucleus, respectively, and four of its seven introduced to replace the structure of diverse and flexible side-chain amino-benzene, design a series of 4 - to replace the aniline-based -6 - methoxy --7 -(2 - hydroxy replace C oxy) quinazoline compounds.

目的:通过各种化学合成方法完成目标化合物4--6-甲氧基-7-(2-羟基取代丙氧基)喹唑啉的合成并对目标化合物进行结构修饰,以期获得高活性的表皮生长因子受体酪氨酸激酶抑制剂。

The results of biological activity research showed that the GLP-1 analogues had great resistance to the degradation by dipeptidyl peptidase and decreased the blood glucose prominently.

生物学活性研究结果显示,改造后的GLP-1类似物能有效抵抗DPP IV的水解,并且有很好的降血糖活性。

Analogues of GLP-1 and Dipeptidy peptidase-Ⅳ inhibitors have a better prospect in the recent study.

其可被二肽基肽酶Ⅳ降解,半衰期极短,限制了其临床应用,目前研究GLP-1类似物及二肽基肽酶Ⅳ抑制剂有更好的应用前景。

The compounds in this paper have been licensed to Pico Pharmaceuticals, which plans to develop and initiate clinical trials of transition-state analogues.

本论文中的化合物已经授权给Pico制药公司,该公司计划开发并启动过渡态类似物的临床实验。

Aim According to the targets of 5-HT transporter and 5-HT2A receptor, a series of N -indolalkyl piperidine derivatives and their analogues were synthesized and tested for their biological activities.

摘要摘 要:目的以5-羟色胺转运体和5-HT2A受体为靶点,设计合成 N -吲哚烷基哌啶类化合物及其类似物,研究它们的体内外生物活性。

It's has been reported that lactoquinomycin and frenolicin B, analogues of kalamycin, can inhibit AKT for the pyran naphthoquinone skeleton they have. We found that although kalamycin has pyran naphthoquinone skeleton, but did not suppress AKT and its downstream signal system, then we make a sytematic analysis on the in vitro anti-tumor effect and mechanism of kalamycin.

有报道其类似物lactoquinomycin和frenolicin B是肿瘤靶点AKT抑制剂,并由此推断吡喃萘醌骨架在AKT抑制过程中发挥主要作用,我们发现虽然卡拉霉素含有吡喃萘醌骨架,但是并不抑制AKT及其下游信号系统;继而对卡拉霉素的体外抗肿瘤作用及其机理进行了系统的分析。

The study of geological analogues is one of the important methods for safety assessments of the radioactive waste repository. It will be a new field for geological research in China.

地质类比研究是安全评价核废物处置系统的重要方法之一,也是地质学科的新研究领域。

Results Among the 103 patients, 65 patients received lamivudine, 29 patients received interferon, and 9 patients received other nucleoside analogues. The results of HBV genotype redetermination indicated that 98 patients' genotypes remained unchanged after the medicine treatment, and genotype analysis failed of success in 5 patients.

结果 103例病人中,65例用拉米夫定治疗,29例用干扰素治疗,9例用其它核苷类药物治疗,停药后复查患者基因类型,除5例未分析出结果外,98例患者通过药物治疗基因类型均未改变。

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从有历史以来,英国,在此地早期居住的是凯尔特人,已经被征服了三次。

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