技術文章/ article

您的位置:首頁  -  技術文章  -  核苷逆轉錄酶 (nucleoside reverse transcriptase) 抑制劑——拉米夫定

核苷逆轉錄酶 (nucleoside reverse transcriptase) 抑制劑——拉米夫定

更新時間:2024-01-12      瀏覽次數(shù):4043

Lamivudine  


CAS號134678-17-4

英文名Lamivudine  

中文名拉米夫定

Synonyms: 拉米夫定; BCH-189

純度99+%

Formula  C8H11N3O3S          分子量  229.26

Appearance   White to off-white solid

生物活性Lamivudine (BCH-189) is an orally active nucleoside reverse transcriptase inhibitor (NRTI). Lamivudine can inhibit HIV reverse transcriptase 1/2 and also the reverse transcriptase of hepatitis B virus. Lamivudine salicylate can penetrate the CNS.

Lamivudine (BCH-189) 是一種具有口服活性的核苷逆轉錄酶 (nucleoside reverse transcriptase) 抑制劑 (NRTI)Lamivudine 可以抑制 HIV 逆轉錄酶 1 2 以及乙型肝炎病毒 (hepatitis B virus) 的逆轉錄酶。Lamivudine 可以透過血腦屏障。

研究領域

Reverse Transcriptase (逆轉錄酶)

Reverse transcriptases (RTs) are enzyme used to generate complementary DNA (cDNA) from an RNA template, a process termed reverse transcription. Reverse transcriptases (RTs) use an RNA template and a short primer complementary to the 3' end of the RNA to direct the synthesis of the first strand cDNA.

Nucleoside reverse transcriptase inhibitors (NRTIs) block reverse transcriptase (an HIV enzyme). Non-nucleoside reverse transcriptase inhibitors (NNRTIs) bind to and block HIV reverse transcriptase. HIV uses reverse transcriptase to convert its RNA into DNA (reverse transcription). Blocking reverse transcriptase and reverse transcription prevents HIV from replicating.

HIV (人類免疫缺陷病毒)

Human immunodeficiency virus

HIV (Human immunodeficiency virus) is a lentivirus (a subgroup of retrovirus) that causes the acquired immunodeficiency syndrome (AIDS), a condition in humans in which progressive failure of the immune system allows life-threatening opportunistic infections and cancers to thrive. Infection with HIV occurs by the transfer of blood, semen, vaginal fluid, pre-ejaculate, or breast milk. Within these bodily fluids, HIV is present as both free virus particles and virus within infected immune cells. HIV infects vital cells in the human immune system such as helper T cells (specifically CD4+ T cells), macrophages, and dendritic cells. HIV infection leads to low levels of CD4+ T cells through a number of mechanisms, including apoptosis of uninfected bystander cells, direct viral killing of infected cells, and killing of infected CD4+ T cells by CD8 cytotoxic lymphocytes that recognize infected cells. When CD4+ T cell numbers decline below a critical level, cell-mediated immunity is lost, and the body becomes progressively more susceptible to opportunistic infections.

Anti-infection (抗感染)

Anti-infectives are drugs that can either kill an infectious agent or inhibit it from spreading. Anti-infectives include antibiotics and antibacterials, antifungals, antivirals and antiprotozoals.

Antibiotics specifically treat infections caused by bacteria, most commonly used types of antibiotics are: Aminoglycosides, Penicillins, Fluoroquinolones, Cephalosporins, Macrolides, and Tetracyclines. New other approaches such as photodynamic therapy (PDT) and antibacterial peptides have been considered as alternatives to kill bacteria.

The high rates of morbidity and mortality caused by fungal infections are associated with the current limited antifungal arsenal and the high toxicity of the compounds. The most common antifungal targets include fungal RNA synthesis and cell wall and membrane components, though new antifungal targets are being investigated.

Viral infections occur when viruses enter cells in the body and begin reproducing, often causing illness. Viruses are classified as DNA viruses or RNA viruses, RNA viruses include retroviruses, such as HIV, are prone to mutate. The currently available antiviral drugs target 4 main groups of viruses: herpes, hepatitis, HIV and influenza viruses. Drug resistance in the clinical utility of antiviral drugs has raised an urgent need for developing new antiviral drugs.

Antiprotozoal drugs are medicines that treat infections caused by protozoa. Of which, malaria remains a major world health problem following the emergence and spread of Plasmodium falciparum that is resistant to the majority of antimalarial drugs. At present, antimalarial discovery approaches have been studied, such as the discovery of antimalarials from natural sources, chemical modifications of existing antimalarials, the development of hybrid compounds, testing of commercially available drugs that have been approved for human use for other diseases and molecular modelling using virtual screening technology and docking.

HBV (乙型肝炎病毒)

Hepatitis B virus

HBV (Hepatitis B virus), abbreviated HBV, is a species of the genus Orthohepadnavirus, which is likewise a part of the Hepadnaviridae family of viruses. HBV causes the disease hepatitis B. The hepatitis B virus is classified as the type species of the Orthohepadnavirus, which contains three other species: the Ground squirrel hepatitis virus, Woodchuck hepatitis virus, and theWoolly monkey hepatitis B virus. The genus is classified as part of the Hepadnaviridae family. HBV is divided into four major serotypes (adr, adw, ayr, ayw) based on antigenic epitopes present on its envelope proteins, and into eight genotypes (A–H) according to overall nucleotide sequence variation of the genome. The genotypes have a distinct geographical distribution and are used in tracing the evolution and transmission of the virus. Differences between genotypes affect the disease severity, course and likelihood of complications, and response to treatment and possibly vaccination.

參考文獻

[1]. Colledge D, et al. Synergistic inhibition of hepadnaviral replication by lamivudine in combination with penciclovir in vitro. Hepatology. 1997 Jul;26(1):216-25.

[2]. Olaniyan LW, et al. Lamivudine-Induced Liver Injury. Open Access Maced J Med Sci. 2015 Dec 15;3(4):545-50.  

[3]. Mdanda S, et al. Zidovudine and Lamivudine as Potential Agents to Combat HIV-Associated Neurocognitive Disorder. Assay Drug Dev Technol. 2019 Oct;17(7):322-329.


CONTACT

辦公地址:中國(上海)自由貿易試驗區(qū)臨港新片區(qū)新楊公路1666號3幢315室 EMAIL:2885066715@qq.com
掃碼關注公眾號
版權所有©2025 凱立德生物醫(yī)藥技術(上海)有限公司 All Rights Reserved   備案號:滬ICP備15046197號-1   sitemap.xml技術支持:化工儀器網(wǎng)   管理登陸

TEL:021-58180488

掃碼關注公眾號
主站蜘蛛池模板: 亚洲av无码潮喷在线观看| 精品人妻无码一区二区色欲产成人| 精品久久久久久无码不卡| 无码精品一区二区三区在线 | 亚洲AV永久无码精品一百度影院| 亚洲中文久久精品无码ww16| 99无码精品二区在线视频| av无码精品一区二区三区四区 | 国产AV无码专区亚洲AV男同 | 无码av免费毛片一区二区| 亚洲AⅤ无码一区二区三区在线| 一本色道久久HEZYO无码| 成人免费无码大片a毛片软件| 久久午夜无码鲁丝片 | 夜夜精品无码一区二区三区| 无码精品人妻一区二区三区免费看 | 日韩AV无码精品人妻系列| 亚洲v国产v天堂a无码久久| 中日韩亚洲人成无码网站| 人妻无码精品久久亚瑟影视| 亚洲另类无码专区丝袜| 久久老子午夜精品无码| 熟妇人妻系列av无码一区二区| 人妻无码aⅴ不卡中文字幕| 无码国内精品久久综合88| 久久久久久AV无码免费网站| 免费无码av片在线观看| 亚洲AV无码乱码精品国产| 亚洲AV无码专区在线厂| 亚洲乱亚洲乱妇无码| 亚洲av永久无码精品秋霞电影秋| 中文字幕无码高清晰| 无码国产乱人伦偷精品视频 | 中文字幕无码无码专区| 亚洲AV无码乱码精品国产| 影院无码人妻精品一区二区| 无码国模国产在线观看免费| 久久久无码精品人妻一区| 婷婷四虎东京热无码群交双飞视频 | 日韩精品无码成人专区| 免费无码又爽又刺激高潮 |