1) inhibition of inhibition
抑制性抑制
2) activity of inhibition
抑制剂抑制活性
3) rejection capability
抑制性
1.
Based on optimizing of frequently used polymers,the orthogonal test method has been adopted to determine the recipe of solid free polymer drilling fluid with strong rejection capability,mainly polyvinyl alcohol(PVA) and compound of inorganic and organic polymers,which can be applied to practical production.
无固相聚合物钻井液是一种抑制性、防塌性能力强的钻井液体系。
2.
The results of soak test,shale expansion test and shale's rolled recovery showed the good rejection capability and anti-collapsing.
结果表明:LG植物胶抑制性强,防塌效果好;4%的LG植物胶能使基浆的润滑系数降低57。
3.
Associative item“Research on strong rejection capability of solid free polymeric drilling fluid system”of the Geology Reconnaissance Station (in short of“GRS”), Jilin province, the purpose of this paper is to triturate dril.
论文结合吉林省地勘局委托项目“强抑制性无固相聚合物钻井液的研制”,研制了适用于吉林省油页岩勘探工作的强抑制无固相聚合物钻井液体系。
4) inhibitive capacity
抑制性
1.
The characteristics, bore hole stabilization mechanism, composition and the use of the mud additives, the evaluation of the shale inhibitive capacity, and the field application of the HPWBM will be discussed in this .
介绍了国外高性能水基钻井液的室内研究和工艺技术方面取得的重要进展,包括其性能特点、井壁稳定机理、组成及处理剂作用、抑制性评价方法和现场应用效果。
2.
An evaluation procedure was required to understand the inhibitive capacity of the inhibitor used.
预防气体水合物危害的通常方法是在深水钻井液中加入水合物抑制剂增强其水合物抑制能力,这就需要对深水钻井液的抑制性有一个合理的评价。
5) inhibitory activity
抑制活性
1.
Synthesis and HIV-1 reverse transcriptase inhibitory activity of 3,4-substituted quinolinone derivatives
3,4-取代喹啉酮类衍生物的合成及其对HIV-1逆转录酶的抑制活性
2.
Primary results showed that some of the compounds displayed potential inhibitory activity at a concentration ranging from 0.
2 mmol/L时部分化合物对该酶有较好的抑制活性。
3.
Various kinds of N-substituted pseudo-aminosugars derivatives,which show more potent inhibitory activity against α-glycosidase than the parent compounds,have been synthesized by chemical modification of pseudo-aminosugars.
井冈霉醇胺、井冈霉胺和井冈胺等假氨基糖类物质是新型的α 糖苷酶抑制剂,对其进行化学修饰可以得到糖苷酶抑制活性更强的N 取代假氨基糖衍生物。
6) inhibiting activity
抑制活性
1.
Synthesis, quantitative structure-activity relationship (QSAR) study of inhibiting activity against Sphaerotheca fuliginea and molecular design of acetophenone oxime derivatives based on quantitative structure-activity relationship were performed.
介绍苯乙酮肟醚类化合物的合成、瓜类白粉病抑制活性的定量构效关系(QSAR)研究以及基于QSAR研究结果的新化合物设计、合成和生测,尝试了农药先导合理设计流程在具有瓜类白粉病抑制活性的苯乙酮肟醚类化合物设计中的应用。
2.
According to the result of biological experiments,2-(4,6-dimethoxy-pyrimidin-2-yloxy)-N-het/aryl-benzylamine derivatives were found to have the inhibiting activity of acetolactate synthase(ALS),and the relationship between these compounds and their activity was studied by 3D-QSAR:CoMFA and CoM-SIA.
生物活性测试结果表明,2-嘧啶氧基-N-芳基苄胺类化合物对ALS具有一定的抑制活性。
3.
When acted with equal proportion of Papain , the inhibiting activity of CPI lost completely; CD spectrum changed remarkably and the content of α-helix declined.
水稻巯基蛋白酶抑制剂(CPI)圆二色性谱(CD)显示206nm和222nm处的双负峰,CPI分子以α 螺旋构象为主;当CPI与木瓜蛋白酶等摩尔结合后,CPI完全丧失抑制活性,复合物CD谱发生显著变化,α 螺旋含量降低。
补充资料：超速抑制
超速抑制
ultraspeed inhibition
正常情况下，窦房结对于潜在起搏点的控制，通过两种方式实现：①抢先占领；②超速抑制。超速抑制即窦房结对于潜在起搏点所产生的一种直接抑制作用。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条