1)anti-HIV agents抗HIV药
英文短句/例句
1.Today's anti-HIV drugs block the virus once it gets into a cell.目前抗HIV药是HIV病毒进入细胞后进行阻止。
2.Design and Synthesis of Anti-HIV Drugs Based on CCR5;以CCR5为靶标的抗HIV药物设计与合成
3.Application of Evidence-based Pharmacy in Rational Use ofAnti-HIV Drugs循证药学在合理使用抗HIV药物中的应用
4.However, some anti-TB drugs interfere with the effect of some anti-HIV drugs.然而，一些抗肺结核药物会对某些抗HIV药物的功能产生影响。
5.Screening and in Vitro Evaluating Anti-HIV-1 Activities of Antagonists of Chemokine Receptor CCR5;抗HIV药物筛选和活性研究及抗癌反义药物机理初探
6.Research on the Synthesis of the Chiral Intermediate of a New Anti-HIV Drug Fosamprenavir;新型抗HIV药物夫沙那韦手性中间体的合成研究
7.Study on Improving Synthesis Technology and Bio-Activity of Anti-Hiv Polysaccharides;抗HIV药用多糖的合成工艺改进及活性研究
8.Establishment and Application of Key Techniques of the Efficiency Evaluation of Anti-retroviral Agents in Vitro抗HIV药物体外药效学研究关键技术的建立和应用
9.While none are yet available in pharmacies, they are probably the most promising new class of anti-HIV drags under review.目前在制药业中还没有一家已制成这类药，它们可能在抗HIV药中被视为最有希望的新一类药。
10.Experimental Study on Anti-HIV-1 Activity of YBF;中药YBF抗HIV-1的实验研究
11.Drug Design Against HIV-1 Targeting Viral Entry Process;阻断病毒进入细胞的抗HIV-1药物设计
12.Efficacy of anti-HIV treatment and drug-resistance mutations in Henan province,China河南省抗HIV治疗效果及耐药变异分析
13.Advances in Research on the Aptamers anti-HIV Drugs核酸适配体类抗HIV-1药物的研究进展
14.Study on the Self-assembled Systems of the Anti-HIV Bolaamphiphilic Prodrug抗HIV双载药双头基两亲前药自组装体的研究
15.Synthesis and Characterization of the Mannose Thio-trisaccharide as Anti-HIV Agent Targeting DC-SIGN;基于DC-SIGN为靶点的抗HIV寡糖药物的合成与表征
16.Molecular designing strategies of anti-drug-resistant HIV-1 protease inhibitors抗耐药性HIV-1蛋白酶抑制剂的分子设计策略
17.Prevalence and Evolution of HIV-1 Drug Resistance in Patients Receiving Free Antiretroviral Therapy in China;我国HIV-1免费抗病毒治疗患者基因型耐药性及耐药进化研究
18.Study on Pharmacokinetics and Chemical Stability of Anti-HIV Nucleoside Prodrugs核苷类抗HIV系列前药的化学稳定性及药物动力学研究
相关短句/例句
anti-HIV agents抗HIV药物
1.Advances in the research of chemokine receptors antagonists as anti-HIV agents;以趋化因子受体为靶点的抗HIV药物研究进展
2.With understanding of mechanism of HIV infection,more and more new anti-HIV agents are developed and used in clinical experiments.随着对艾滋病致病机制的深入研究,越来越多新的抗艾滋病病毒(HIV)药物进入临床试验,但大量抗HIV药物的应用也导致了耐药性问题的出现。
3)anti-HIV drugs抗HIV药物
1.Application of three-dimensional quantitative structure-activity relationship in design of anti-HIV drugs本文对三维定量构效关系技术在抗HIV药物中的应用做一总结和展望。
4)anti-HIV agent抗HIV病毒药
5)anti-HIV natural drugs抗HIV天然药物
6)anti-HIV抗-HIV
1.Method Reitman s method was taken for the test of ALT, and ELISA was for HbsAg, anti-HCV, anti-HIV and serum test of syphilis.方法丙氨酸氨基转移酶(ALT)检测采用赖氏法,HBsAg、抗-HCV、抗-HIV和梅毒血清学检测均采用ELISA检测。
2.Methods Serum levels of five HBV markers, anti-HCV, anti-HIV (with ELISA) and ALT were determined in 214 hospitalized patients before forthcoming blood exposure as well as in 2468 controls.方法:采集病人及一般人群的血清运用酶联免疫吸附试验(ELISA)及ALT速率法进行HBV标志物五项、抗- HCV、抗-HIV及ALT检测。
延伸阅读
抗真菌药和抗立克次氏体药抗真菌药和抗立克次氏体药Chemotherapeutics, Antimycotic and Antirickettsial kans抗真菌药和抗立克次氏体药第9卷 O }}(1)CICH之一C一CHZCI一-~甲~~~~~叫~~一~~~(2)CHaC00H FB了IJ ︸胜、!尸以.纵扮!F(48) OH lCICH:一C一CHZCIN=，、 1，1 NH尸丫r，一一三之~、汗尸Na月，DMF F(49)(11) :HzN~3。:。您丫督自气丛立竺竺自护、-跳沪/、‘犷HCOH、屯/卜‘2 (51)(52) 。之丫⑧ 坐助OH(‘2，(53) HCI-~~，~~~~~~，..~ 一H20‘HCI(90)侧 月F C.\H一\l尸n下.C上z、丫F H C 一 N =‘ N 1.1七(47) 氟康哇口服吸收快而完全，半衰期长(22~32h)体内分布均匀，能很好的透过血脑屏障，并渗透到脑脊液内阳〕。口服100mg后，脑脊液平均浓度为血浆浓度的0.58一0.89倍。70%原药由肾脏排除。 大多数病人对氟康哇耐受良好哪〕。常见的副作用为头痛、恶心、疲劳、发热、浮肿、出疹、腹部不适及转氨酶升高。但发生率小于5环，极少数病人出现血小板减少，停药后即恢复。·2.8.烯丙胺类 1981年发现蔡替芬(haftifine)(s0)具有较高的广谱抗真菌活性。由于其优良的抗真菌活性，新颖的结构特点，很快引起了人们的重视，通过对其结构改造和抗菌活性的研究，发现了活性高、毒性低的衍生物特比禁芬(terbinafine)(‘oa)和丁禁芬(botenafine)(乐ob)。活性最大，最低抑菌浓度(Mlc)为。.01一0.2哆/ml，对申克氏抱子丝菌和曲霉属真菌次之，Mlc分别为0.8一1.5限/耐和0.8~12.5阳/而。禁替芬的体外抗皮肤真菌活性明显优于咪哇类抗真菌药，而与托蔡醋(发癣退)和灰黄霉素相似。 蔡替芬对真菌细胞超微结构有影响，还干扰真菌细胞的脂质代谢，故有杀菌作用。在作用机理上蔡替芬与氮哇类药物一样，都是抑制麦角幽醇的生物合成，但作用部位二者不同，禁替芬是角拨烯的环氧化酶的特异性抑制剂。通过抑制角鳖烯的环氧化，使角盆烯蓄积和麦角幽醉缺乏，使真菌细胞膜的组成和通透性发生改变，导致杀菌作用[5，〕。 蔡替芬是一个高效低毒的外用抗真菌药，其疗效与克霉哇、美康哇、益康哇等外用抗真菌药相似。
