1)antifungal peptide抗真菌肽
1.Antifungal activity and the immunogenicity of antifungal peptide Drosomycin and its isoforms from Drosophila melanogaster;黑腹果蝇抗真菌肽Drosomycin同系物的免疫原性和抗真菌活性
2.Soluble expression of the antifungal peptide genes,Drs and Drs-lC,of Drosophila melanogaster in the prokaryote and the detection of their antifungal activity;黑腹果蝇抗真菌肽基因Drs和Drs-lC的原核可溶性表达及抗真菌活性测定
3.The relationships between the structure and function of insect antibacterial peptides and antifungal peptides and molecular design;昆虫抗菌肽和抗真菌肽结构与功能的关系及分子设计
英文短句/例句
1.Purification, Characterization and Antibiotic Property of Natural Antifungal Peptide APS;天然抗真菌肽APS的分离纯化、理化特性及其生物活性研究
2.The Expression Analysis of Paralichthys Olivaceus Hepcidin Gene and the Antibacterial Effects of Pagrus Major Recombinant Antimicrobial Peptide;牙鲆抗菌肽Hepcidin基因的表达分析及真鲷重组抗菌肽的抗菌活性研究
3.Construction of Eukaryotic Expression Vector of Antimicrobial Peptide Gene Defensin抗菌肽Defensin基因pcr3.1真核表达载体的构建
4.Cloning, Expression and Antimicrobial Activity Analysis of Hepcidin Gene Variants in Two Cultured Fish, Pagrus Major and Spagrus Macrocephalus;养殖真鲷、黑鲷抗菌肽hepcidin的基因克隆、表达特性及其抗菌活性研究
5.Construction and Bioactivity of Eukaryotic Recombiant Plasmid of Novel Fusion Gene of Antibacterial Peptide;新型融合抗菌肽基因重组真核质粒的构建及抗菌活性研究
6.Secreted Expression and Activity Detection of Two Hybrid Antimicrobial Peptides in Pichia Pastoris;杂合抗菌肽的设计改造、真核表达及性质研究
7.Construction of eukaryotic expression vector encoding antimicrobial peptides PR-39 and its expression in 293T cell抗菌肽PR-39真核表达载体的构建及表达检测
8.cDNA Clone of Antimicrobial Peptide from the Reproductive Tract of Ovis aries and Construction of its Eukaryotic Expression Vector绵羊生殖道抗菌肽cDNA克隆及真核表达载体构建
9.The Study on Antimicrobial Activity Against Plant Pathogenic Fungi and Prefractionation of Antimicrobial Peptides from Insects昆虫抗菌肽对植物病原真菌的抑菌活性及其初步分离的研究
10.Purification and Characterization of Antifungal Peptide from Isaria Felina and Antifungal Protein from Tricholoma Giganteum;猫棒束孢菌抗真菌多肽和巨大口蘑抗真菌蛋白的分离纯化及特性的研究
11.Fermentation, Purification and Study of a Low Molecular Factor with Antimicrobial Activity by Fungi;真菌产生的低分子抗菌肽的发酵生产、分离纯化及其性质研究
12.Purification and Structural Identifications of the Antifungal Lipopeptides Produced by Marine Bacterium Bacillus subtilis 3512A海洋枯草芽孢杆菌3512A抗真菌脂肽的分离纯化及结构特性鉴定
13.Antibacterial and Anticancer Peptides in Batrachia Skin Secretion蛙类皮肤分泌物中的抗菌肽和抗癌肽
14.Research progress of buforin Ⅱ,a histone H_2A-derived peptide抗菌肽buforinⅡ的研究进展
15.The Research of Novel Chlorin Photosensitizers and Cyclohexalipopeptide of Antifungal Agents;新型二氢卟吩类光敏剂及环六脂肽类抗真菌药物的研究
16.Construction of Eukaryotic Expression Vector of Antibacterial Peptide and Its Preliminary Application to the Gene Therapy in Tumor;抗菌肽ABPS1真核表达载体的构建及其在肿瘤基因治疗中的初步应用
17.Construction of Recombinant Expression Vector of Sea Bream and Its Expression in Yeast Pichia Pastoris;真鲷抗菌肽基因重组表达载体的构建及其在酵母中的表达
18.Design an Antibacterial Peptide by Studying on Granulysin s Antibacterial Mechanism;依据Granulysin的抗菌机理合理设计抗菌肽
相关短句/例句
Antifungal peptide gene抗真菌肽基因
3)antifungal peptide APS抗真菌多肽APS
4)Natural antifungal peptide天然抗真菌肽
5)Insect antifungal peptides昆虫抗真菌肽
6)antibacterial peptides抗菌肽
1.Effect of antibacterial peptides extracted from musca domestica pupa on membrane of cancer cell;家蝇蛹抗菌肽对肿瘤细胞膜破坏作用
2.An animal model of transgenic mice with expression of antibacterial peptides;抗菌肽转基因小鼠模型的建立
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。
