采用正交试验方法，分析了生物抑制剂对龙眼果皮褐变和保鲜效果的影响。
Using orthogonal experiment, the effects of biological inhibitors on longan pericarp Browning and the freshness quality were analyzed.
通过本文的研究为以后开发糖苷酶抑制剂药及生物农药提供了一定的理论基础。
All of studies in this dissertation offer references to research and development of glycosidase inhibitor medicine and bio-pesticide.
选择性COX - 2抑制剂可联合化疗、内分泌治疗及生物治疗等，作为肿瘤治疗的辅助药物应用于临床，为乳腺癌的治疗提供一种新的途径。
Selective COX-2 inhibitors can combine with chemotherapy, endocrine therapy and biotherapy. It is gradually used for adjunctive therapy and provides a new pathway for the therapy of breast cancer.
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.
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.
端粒、端粒酶及其抑制剂研究是分子细胞生物学以及医学的热点之一。
Telomere, telomerase and its inhibitors are being extensively studied in the field of molecular and cellular biology and medicine.
唑类和三氮唑类药物作为细胞色素P 450抑制剂广泛被作为抗真菌药物和抗微生物药物使用。
Azole and triazole drugs are cytochrome P450 inhibitors widely used as fungal antibiotics and possessing potent antimycobacterial activity.
PTK787因其对肿瘤抑制的出色疗效、口服生物利用度高等特点而成为VEGF受体酪氨酸激酶抑制剂中的佼佼者。
PTK787 is the most promising VEGF receptor- tyrosine kinase inhibitor in pipeline because of its potency in tumor inhibition and oral bioavailability.
目的从微生物代谢物中筛选中性鞘磷脂酶抑制剂。
OBJECTIVE to screen neutral sphingomyelinase inhibitors from the metabolites of microorganism.
本文通过分子生物学和生理生化两个角度对ALS抑制剂与ALS作用机理进行了初步的研究。
In this paper, the function mechanisms of acetolactate synthase (ALS) inhibitors to ALS had been carried out, using the methods of molecular biology, physiology and biochemistry.
背景：血小板对氯吡格雷的反应性存在异质性，而且以氯砒格雷作为次选血小板抑制剂的临床或生物化学预测尚不清楚。
Background: a heterogeneous platelet reactivity response to clopidogrel exists, and the clinical or biochemical predictors of suboptimal PI with clopidogrel remain unclear.
研究了几种生长抑制剂对猕猴桃幼旺树成花的生物学效应和生物化学效应。
The effect of controlling biological and biochemical characters upon young Chinese gooseberry trees was studied using growth inhibitors for controlling floral initiation.
经过系统药理学研究表明，该生物碱具有良好抗胆碱酯酶效应，从而可认为该生物碱系一种新结构类型的可逆性胆碱酯酶抑制剂。
The systematic pharmacological study shows that this alkaloid possesses good anticholinesterase effect, and therefore it is a new structure type of reversible acetylcholinesterase inhibitor.
还对分化诱导剂、拓扑异构酶抑制剂、抗微管药和生物反应调节剂的筛选方法进行了评述。
In addition, the paper reviewed screening methods for differentiation inducers, DNA topoisomerase inhibitors, antimicrotubule drugs and biological response modifiers.
本文对其生物活性物质，尤其蛋白酶抑制剂的理化性质及其功能等进行了综述。
The recent developments on bioactive compounds from buckwheat, especially the physicochemical property and function of protease inhibitor, are reviewed in this paper.
这书提供一蛋白酵和他们抑制剂在瘤生物学的行动的机制的综合评估。
This book provides a comprehensive evaluation of the mechanisms of action of proteases and their inhibitors in tumor biology.
我们专注于提供最近所描述的生物化学通路的抑制剂。
We focus on providing inhibitors of recently described biochemical pathways.
本文主要概述了微生物来源的醛糖还原酶抑制剂的研究进展。
This review mainly gives a brief account of the progress of research on aldose reductase inhibitors from microorganisms.
目前临床上对重症溃疡性结肠炎患者的治疗多采用糖皮质激素、免疫抑制剂、生物制剂和抗生素等，使病情得到缓解。
Currently, glucocorticoids, immunosuppressants, biological reagents and antibiotics are used to treat severe ulcerative colitis, and induce the remission in the clinic.
本文综述了包括肿瘤坏死因子抑制剂、白细胞介素1抑制剂、干细胞移植及基因治疗等生物治疗在类风湿性关节炎治疗中的作用。
This article reviews the effect of biotherapy in ra including tumor necrosis factor inhibitor, IL-1inhibitor, stem cell transplantation genetic therapy and so on.
新颖的1，2，3-取代的中氮茚衍生物，FGF抑制剂，制备它们的方法和含有它们的药物组合物。
Novel 1, 2, 3-substituted indolizine derivatives, inhibitors of FGFs, method for making same and pharmaceutical compositions containing same.
COX - 2及其抑制剂在肿瘤预防、放疗、化疗、生物疗法中具有广阔应用前景。
COX-2 and its inhibitors have a broad prospect in the tumor prevention, chemotherapy, radiotherapy and biotherapy.
本发明涉及作为组蛋白脱乙酰基酶（HDAC）抑制剂的异羟肟酸衍 生物。
The present invention relates to hydroxamic acid derivatives that are inhibitors of histone deacetylase (HDAC).
糖蛋白抑制剂可促进药物通过血脑屏障，对提高脑内药物的浓度和中枢神经系统药物的生物利用度具有重要意义。
P-glycoprotein inhibitors can get drugs across the blood-brain barrier. It is of great importance to improve the blood concentration in brain and bioavailability of central nervous system drugs.
随着分子生物学研究的进展，表皮生长因子受体抑制剂、血管内皮生长因子抑制剂等分子靶向药物的研究成为热点之一。
With the advancement of the study of molecular biology, the research of the molecular targeted drugs such as EGFR inhibitor and VEGF inhibitor, become one of the hot spots.
用作高选择性环加氧酶-2抑制剂的二芳基1,2,4 -三唑衍生物。
Diaryl 1, 2, 4-triazole derivatives as a highly selective cyclooxygenase-2 inhibitor.
寻找及发现其抑制剂是研究它的生物学功能的重要途径。
The specific inhibitors of DNA topoisomerases are the useful tool in studying their biological functions.
目的研究纤溶酶原激活物抑制剂(PAI1)与肝细胞癌(HCC)生物学特性的关系。
Objective to study the relationship between plasminogen activator inhibitor type 1 (PAI 1) and biological behaviour of hepatocellular carcinoma (HCC).
布雷非德菌素是一种高效的细胞生长抑制剂。1958年第一次被报导，之后又被几个研究小组在一系列不同的生物化验中作为高效活性试剂。
Brefeldin a is a potent inhibitor of cell growth first described in 1958, then independently "rediscovered" by several groups as a potent active in a broad range of bioassays.
扶素生物自主开发的第一个产品：艾滋病病毒膜融合抑制剂——西夫韦肽。
The lead drug candidate in FusoGen's pipeline is Sifuvirtide, an HIV fusion inhibitor. One of the first fusion inhibitor drug against HIV.
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