几丁质生物合成抑制剂，1型，同翅目昆虫。
用RNA和蛋白质合成抑制剂预处理神经元，可阻断其死亡。
RNA and protein synthesis inhibitors blocked the neurotoxicity induced by bilirubin.
蛋白合成抑制剂亚胺环己酮可以诱导小鼠卵母细胞发生孤雌活化，但其机制尚未完全阐明。
Cycloheximide(CHX), a protein synthesis inhibitor, can activate mouse eggs but the underlying mechanism is not fully known.
本文综述了近年来农药中色素合成抑制剂的作用机制及最新应用进展，并展望未来的发展趋势。
The mechanism of target enzymes, the latest application and development trends in the future were summarized.
对苯甲酰基脲类几丁质合成抑制剂的结构、合成方法、作用机制、代谢及环境安全性等进行了评述。
The structures, synthetic methods, insectical mechanism, degradation, together with environmental safety of benzoyl urea chitin synthesis inhibitors were reviewed in this paper.
蛋白质合成抑制剂乙基硫氨酸和对-氟苯丙氨酸能抑制冬小麦的春化，抑制时期也是在春化过程的中期。
The protein metabolic inhibitors, such as ethionine and p-fluorophenylalanine, interfere with the vernalizing process of winter wheat also at its middle period.
介绍了水合物抑制剂hbh的合成工艺，对其水合物抑制性及与其它处理剂的配伍性进行了室内评价。
In this paper, synthetic technology of hydrate inhibitor HBH is presented and its inhibitive property and compatibility with other additives are also evaluated in laboratory.
针对抑制MMP的治疗方法展开了深入的研究，合成的mmp抑制剂在肿瘤的浸润与转移的治疗中将有广阔的前景。
With further research on inhibition of MMP, synthetic MMP inhibitor will have good prospects in the treatment of tumor invasion and metastasis.
综述了胆固醇生物合成过程及生物合成过程中关键酶抑制剂的研究开发现状。
Cholesterol biosynthetic pathway, status of research and development on inhibitors of key enzymes in cholesterol biosynthesis were reviewed.
该法原则上适用于多种HIV蛋白酶抑制剂的合成。
It is appropriate to the synthesis of lots of HIV protease inhibitors in principle.
采用平行-连续法合成了HIV蛋白酶抑制剂沙奎那韦。
Synthesis of saquinavir, an HIV protease inhibitor, was researched via convergence method.
目的：合成GABA摄取抑制剂盐酸噻加宾。
Objective: to synthesize tiagabine hydrochloride, a GABA uptake inhibitor.
目的：合成COX-2抑制剂戊地昔布。
目的对细菌脂肪酸生物合成所涉及到的酶及其抑制剂的筛选研究进行综述。
Objective To review the research development of the enzymes involved in the bacterial fatty acid biosynthesis and their inhibitors.
正常的有机体会合成一系列抑制剂，来阻止不希望的水解。
Normal organic will synthesize inhibitors to prevent from unhopeful hydrolysis.
影响二恶英从头合成的因素有碳源、氯源、氧气、水、颗粒表面特性、温度、停留时间、催化剂和抑制剂等。
The influenced factors of denovo synthesis of dioxins may be carbon, chlorine, oxygen, water, nature of the ash's surface, temperature, residence time, catalyzer and inhibitor, etc.
本文综述缺血性视网膜损伤机制，一氧化氮特性及与缺血性视网膜损伤的关系，一氧化氮合成酶抑制剂的作用等。
This paper had summarized the mechanism of ischemic retinal injury, relationship between the characteristic of NO and ischemic retinal injury and action of NO synthetase inhibitor.
NO合成酶抑制剂可能为高no水平的不孕妇女提供新的治疗途径。
NO synthetase inhibitor may provide a new therapy for infertility women with high NO level.
结论NO与偏头痛发作有密切关系，应用NO合成酶抑制剂有助于偏头痛的治疗。
Conclusion the NO is closely related to the attack of migraine, and NO synthetase depressor can help the treatment of it.
目的合成新型吡咯烷类神经氨酸酶抑制剂，并测定其抑制神经氨酸酶的活性。
OBJECTIVE To synthesize a series of novel pyrrolidine derivatives as neuraminidase inhibitors and test their inhibitory activities against neuraminidase.
目的合成一种新型的多激酶抑制剂。
目的：合成基质金属蛋白酶抑制剂伊洛马司他。
Objective: To synthesize ilomastat, a matrix metalloproteinase inhibitor.
本论文设计合成了一类新结构的PK B抑制剂。
This dissertation described the research process of a new class structure of the PKB inhibitors.
IAA合成及运输抑制剂明显降低3H-葡萄糖在籽粒中的分配。
IAA inhibitors decreased IAA contents in both superior and inferior spikelets and reduced 3H glucose radiaton activity.
设计并合成了一种可以抑制硫化矿的小分子有机抑制剂甘油基黄原酸钠，通过浮选试验考察了该抑制剂对硫化矿物的浮选抑制行为。
A small molecular organic depressant, glyceryl-xanthate sodium, was designed and synthesized, and its behavior in depressing sulfide minerals was investigated by flotation tests.
本文用支持矢量学习机和神经网络两种机器学习方法建立选择性环氧化酶-2抑制剂的活性预测模型，以期为选择性环氧化酶-2抑制剂药物的合成提供先导化合物。
Machine learning methods, including Support Vector Machines and Artificial Neural Network, are applied to the development of the classification models for the selective COX-2 inhibitors in this paper.
结果：得到了具有天然活性的泛酸合成酶，建立并优化了酶活测定体系及筛选模型，应用模型筛选得到了具有新结构的抑制剂。
Results: the recombinant PS had nature activity. The system of enzyme activity was build and optimized. A novel PS inhibitor was found by the screening.
Slentrol是一种新型化学物质，选择性微粒体甘油三酸酯转移蛋白抑制剂，阻断脂蛋白在血液中的合成和释放。
Slentrol is a new chemical entity called a selective microsomal triglyceride transfer protein inhibitor, which blocks the assembly and release of lipoproteins into the bloodstream.
Slentrol是一种新型化学物质，选择性微粒体甘油三酸酯转移蛋白抑制剂，阻断脂蛋白在血液中的合成和释放。
Slentrol is a new chemical entity called a selective microsomal triglyceride transfer protein inhibitor, which blocks the assembly and release of lipoproteins into the bloodstream.
应用推荐