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analogs相关的网络例句

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与 analogs 相关的网络例句 [注:此内容来源于网络,仅供参考]

These results suggest that inositol 1, 3, 4-trisphosphate 5/6-kinase or its analogs may be involved in the osmotic stress response in Arabidopsis in stress signaling pathways dependent on and/or independent of abscisic acid.

这些结果表明,编码1,3,4-三磷酸肌醇5/6-激酶类似物的拟南芥基因家族的不同成员可能参与了依赖于ABA和不依赖于ABA的胁迫信号传递途径。

The new methods allow a wide range of poly analogs to be obtained in few steps, as the allylic precursors are readily available.

新方法允许范围广泛的聚类似物,以获得在几个步骤,作为烯前体是现成的。

Allylic side chain was modified to give six bayin analogs in which compound I has a free 7-hydroxy group.

修饰8-位烯丙基侧链,得到了六个黑豆素类似物,共中8的7-位为游离羟基。

But the prognosis is always poor. Artemisinin and its analogs have been used widely as antimalaria drugs and considered to be safe drugs without obvious side effects.

青蒿素及其衍生物是安全有效的抗疟疾药物,近来发现其具有较好的抗肿瘤作用。

Starting from 3-benzoyl-5-formyl-indolizine, 3-benzoyl-5-(2'2'-diacetylethenyl)-indolizines and analogs were obtained by the 〓mediated aldol condensation or Wittig reaction. These compounds,promoted by low-valent titanium, gave highly functionlizedcycl[3,2,2]azine derivatives. The coupling reaction proceeded betweenthe carbonyl group and the carbon-carbon double bond, a rare example inMcMurry reaction.

我们以3-苯甲酰基-5-甲酰基中氮茚为原料,通过三碘化钐促进的aldol反应和Wittig反应制备了3-羰基-5-羰基乙烯基中氮茚,随后经低价钛还原偶联,没有生成正常的分子内羰基-羰基偶联产物,而是得到反常的羰基与α,β-不饱羰基的双键偶联产物,较高收率地得到了含多官能团的CycI[3,2,2]azine衍生物。

Following developments in electrical theories such as Coulomb's law , which showed that positive and negative charges attract, analogs in human life were developed, such as "opposites attract."

随着电学理论的发展,例如库仑定律的提出表明异种电荷相互吸引,类似的概念在人类生活中也被提出,例如"异性相吸"。

In some cases, its epimer 4 was also obtained. 22 compounds were synthesized, among them 18 were new.3. Using the intramolecular Pictet-Spengler reaction to form the pentacyclic skeleton of Et-743, the byproducts 25 were obtained under various conditions. The structures of them were determined to be 1, 2-dihydro-isoquinoline compounds, and the mechanism of the reaction was proposed.B. The synthesis of the analogs of Et-743Because of the failure of removing the protective groups in compounds 14, the synthetic strategy was adjusted.

对于苄基保护的羟基化合物13a,顺利得到化合物30,然后与不同的羧酸反应得到18个酯化合物33-50;对于苄氧羰基保护的氨基化合物13b,由于脱除保护基的化合物31在空气中不稳定,所以我们采取不经分离纯化,直接与羧酸反应得到酰胺化合物53-62,然后再分别对其C-21位的羰基进行还原氰基化,得到10个酰胺目标化合物63-72,另外,我们还对羟基转化为氨基的反应进行了探索。3。

In this study, curcumin and 23 novel analogs were used to screen for inhibition of matrix metalloproteinase-9 (MMP-9) activities, protein and gene expression of highly metastatic HT-1080 human fibrosarcoma cells to explore the mechanisms of action.

本篇研究使用姜黄素及其二十三个结构类似物对於具有高度转移活性的人类纤维肉瘤细胞(HT-1080)进行MMP-9活性、蛋白质及基因表现抑制活性筛选,并探讨其可能机制。

The amide local anesthetics andthe amide analog enhanced diazoxide-induced flavoproteinfluorescence by 5% to 20%, whereas ester local anesthetics decreaseddiazoxide-induced flavoprotein fluorescence by 5% to 60% andthe non-amide local anesthetic analogs had no effect.

酰胺类局麻药及其类似物可使二氮嗪激发的黄素蛋白荧光增强5%到20%,而酯类局麻药可使二氮嗪激发的黄素蛋白荧光减弱5%到60%,非酯类局麻药类似物无影响。

On the basis of the previous research of Annonaceous Acetogenins in ourgroup, the doctoral dissertation describes the design and synthesis of analogs of bis-THF AA such as Isochermolin and Membranacin.The study on these analogs andthe natural product Annonacin complex with metal ion by NMR has been carriedout.

本论文是在我们小组进行番荔枝内酯类似物的基础上,设计合成了一系列双四氢呋喃环番荔枝内酯类似物,并通过核磁共振等手段研究了类似物和天然产物Annonacin与钙离子的络合特性。

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