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inhibitor     
相关语句
  抑制剂
     Isolation and Identification of theα-Glucosidase Inhibitor from Macroalgae and Studies of Inhibition Mechanism
     海藻中α-葡萄糖苷酶抑制剂的分离鉴定及其活性机理的研究
短句来源
     Experimental study of endothelin converting enzyme inhibitor [D-Val22] big ET-l(16-38) for the prevention and treatment of cerebral vasospasm
     内皮素转化酶抑制剂-[D-Val~(22)]大ET-1(16-38)预防和治疗脑血管痉挛实验研究
短句来源
     Expression of COX-2 Gene in Human Prostate Cancer Cells and the Effect of Selective COX-2 Inhibitor
     COX-2基因在人前列腺癌细胞中的表达及其选择性抑制剂的作用研究
短句来源
     Study on the Mechanism of Urinary Trypsin Inhibitor Attenuates Hepatic Cold Ischemia-reperfusion Injury in Mice
     尿胰蛋白酶抑制剂减轻小鼠肝脏冷缺血再灌注损伤的作用机制研究
短句来源
     Study of the Difference in Anti-proliferative Potency of a New Thymidylate Synthase Inhibitor Nolatrexed and Its Mechanism
     新型胸苷酸合成酶抑制剂洛拉曲克抗增殖作用的差异及其机理的研究
短句来源
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  缓蚀剂
     Applied Research on Inhibitor of Internal Combustion Engine Coolant
     内燃机冷却液缓蚀剂的应用研究
短句来源
     The Relationship between the Molecular Structures of Organic Inhibitor and Their Efficiency
     有机缓蚀剂的结构和缓蚀率之间的关系
短句来源
     THE STUDY OF “7801”,A CORROSION INHIBITOR FOR STEEL IN CONCENTRATED HYDROCHLORIC ACID AT HIGH TEMPERATURE
     高温浓盐酸缓蚀剂—“7801”的研究
短句来源
     THE CRITICAL PASSIVATION CONCENTRATION OF VANADATE INHIBITOR IN HOT POTASSIUM CARBONATE SOLUTIONS
     热钾碱溶液中钒酸盐缓蚀剂的临界致钝浓度
短句来源
     Corrosion Inhibition and Mechanism of PC—602 Inhibitor on Carbon Steel in NaCl Solution
     PC-602缓蚀剂对氯化钠溶液中碳钢的缓蚀作用与机理
短句来源
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  抑制物
     A Case of Deficiency of Plasma Plasminogen Activator Inhibitor 1, Its Diagnosis, Treatment and Study on Molecular Abnormality
     遗传性纤溶酶原激活剂抑制物-1缺乏症的诊断、治疗及发病机理的研究
短句来源
     The Study of Plasminogen Activator Inhibitor 1 mRNA Expression in Aged Rat's Cerebral Cortex and Liver with Acute Alcoholism
     老龄大鼠急性酒精中毒时大脑及肝脏组织中Ⅰ型纤溶酶原激活物抑制物mRNA表达的研究
短句来源
     AN EXPERIMENTA L STUDY OF α_2—PLASMIN INHIBITOR
     α_2纤溶酶抑制物的实验研究
短句来源
     Isolation of Human Serum Cl Inhibitor Antigen
     人血清中补体成分C_1~-抑制物抗原的分离
短句来源
     STUDIES ON GABA-T AND ITS INHIBITOR IN MICE WITH HEPATIC ENCEPHALOPATHY
     肝性脑病小鼠GABA—T及其抑制物的研究
短句来源
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  抑制因子
     the phosphorylation level of Smad2C and Smad3L decreased in the cells treated with JNK inhibitor (3,10 μmol) and p38 inhibitor (1,3,10 μmol);
     JNK抑制因子(3、10μmol)与p38抑制因子(1、3、10μmol)可明显抑制Smad2C、Smad3L磷酸化,ERK抑制因子(1、3、10μmol)对Smad2/3磷酸化无明显影响。
短句来源
     Objective:To investigate the in vitro effects of Ganshuang Keli on gene and protein expression of collagenⅠ(ColⅠ),collagenⅢ(ColⅢ)and tissue inhibitor of metalloproteinase 1(TIMP1)in HSC-T6 cell.
     目的:观察肝爽颗粒对HSC-T6细胞Ⅰ型胶原(CollagenⅠ,ColⅠ)、Ⅲ型胶原(CollagenⅢ,ColⅢ)、基质金属蛋白酶组织抑制因子1(Tissue Inhibitor of Metalloproteinase1,TIMP1)基因及蛋白表达的影响。
短句来源
     Construction and Characterization of Plasminogen Activator Inhibitor Mutant (E350G , E351K)
     纤溶酶原激活物抑制因子-1突变体E350G,E351K的构建及性质研究
短句来源
     Expression and Clinical Significance of Cyclin Kinase Inhibitor P21~(WAF1) and P27~(KIP1) in Children with Acute Leukemia
     细胞周期蛋白依赖激酶抑制因子P21~(WAF1)、P27~(KIP1)在急性白血病的表达及其意义
短句来源
     Correlation of Expression of Ki67 Antigen (Ki67)、Matrix Metalloproteinase 2 (MMP-2)、Tissue Inhibitor of Matrix Metalloproteinase-2 (TIMP-2)、CD147、Laminin Receptor (LN-R) with Invasive Pituitary Adenomas
     Ki67核抗原、MMP-2(基质金属蛋白酶-2)、TIMP-2(基质金属蛋白酶-2抑制因子)、CD147、LN-R(层粘连蛋白受体)的表达与侵袭性垂体腺瘤的关系
短句来源
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  inhibitor
We designed an isatin lead compound as a novel non-nucleoside reverse transcriptase inhibitor with broad-spectrum chemotherapeutic properties for the effective treatment of AIDS and AIDS-related opportunistic infections.
      
Since amlodipine besylate is a very potent inhibitor of both cholinesterases, amlodipine besylate may, like donepezil, be useful in Alzheimer's disease treatment.
      
Efavirenz is a trifluoromethylated inhibitor of human immunodeficiency virus type 1 (HIV-1) reverse transcriptase (RT) that shows good results in anti-HIV chemotherapy.
      
Molecules 6f, i, and j inhibited only COX-1, and the disubstituted ethoxy derivative (6g) was inactive as a COX inhibitor (≤ 100?μM).
      
The study indicated that their antiproliferative activity is largely explained by the steric factors of the substituents, highlighting the role of the size and shape of the inhibitor in forming effective binding interactions with histone deacetylase.
      
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