Aiken Christopher, Chen Chin Ho
Department of Microbiology and Immunology, Vanderbilt University School of Medicine, Nashville, TN 37232, USA.
Trends Mol Med. 2005 Jan;11(1):31-6. doi: 10.1016/j.molmed.2004.11.001.
Betulinic acid (BA) derivatives are low molecular weight organic compounds synthesized from a plant-derived natural product. Several BA derivatives are potent and highly selective inhibitors of HIV-1. Depending on the specific side-chain modification, these compounds function by inhibiting HIV fusion or, as recently demonstrated, by interfering with a specific step in HIV-1 maturation. BA derivatives have potential as novel HIV-1 therapies, and additional studies of their mechanisms of action are likely to further define the novel targets of these compounds and elucidate the basic biology of HIV-1 fusion and maturation. In this review, recent studies of the novel mechanisms of action of this interesting class of antiviral compounds are discussed.
桦木酸(BA)衍生物是由植物源天然产物合成的低分子量有机化合物。几种BA衍生物是HIV-1的强效且高度选择性抑制剂。根据特定的侧链修饰,这些化合物通过抑制HIV融合发挥作用,或者,如最近所证实的,通过干扰HIV-1成熟的特定步骤发挥作用。BA衍生物有作为新型HIV-1疗法的潜力,对其作用机制的进一步研究可能会进一步明确这些化合物的新靶点,并阐明HIV-1融合和成熟的基础生物学。在这篇综述中,将讨论这类有趣的抗病毒化合物新作用机制的最新研究。