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CCR5阻滞剂马拉韦罗的药理与临床评价 被引量:1

Pharmacology and clinical evaluation of maraviroc,a CCR5 antagonist
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摘要 马拉韦罗是一种选择性、可逆的小分子抑制剂,能与细胞膜表面人化学趋化因子受体-5(CCR5)和HIV-1gp120相互作用,抑制CCR5-tropic HIV-1病毒进入细胞,是一种很有前途的新型抗病毒药。现对其药理作用、药动学、药物相互作用及对仅感染CCR5-tropic HIV-1的成年患者的疗效和安全性进行了综述。 Maraviroe is a selective, slowly reversible, small molecule antagonist that interacts with human CCR5 and HIV-1 gp120, and prevents CCR5-tropic HIV-1 entry into cells. In this paper, we reviewed the pharmaeology, pharmacokinetics and drug interactions, the efficacy and safety in the treatment for adult patients infected only with detectable CCR5-tropie HIV-1.
出处 《中国新药杂志》 CAS CSCD 北大核心 2008年第17期1544-1547,共4页 Chinese Journal of New Drugs
关键词 CCR5-tropic HIV-1 马拉韦罗 抗病毒药 CCR5抑制剂 CCR5-tropic HIV-1 maraviroc antiviral drug CCR5 antagonist
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参考文献8

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同被引文献3

  • 1NOTARI S,TOMMASI C,NICASTRI E,et al.Simultaneousdetermination of maraviroc and raltegravir in human plasma byHPLC-UV[J].IUBMB Life,2009,61(4):470-475.
  • 2PATRICK DORR,MIKE WESTBY,SUSAN DOBBS,et al.Maraviroc(UK-427,857),a potent,orally bioavailable,andselective small-molecule inhibitor of chemokine receptor CCR5with broad-spectrum anti-human immunodeficiency virus type 1activity[J].Antimicrob Agents and Chemother,2005,49(11):4721-4732.
  • 3王珍燕,卢洪洲.抗HIV新药--CCR5拮抗剂马拉韦罗[J].中国艾滋病性病,2008,14(4):431-434. 被引量:3

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