MACROLIDES DERIVATIVES AS ANTIBACTERIAL AGENTS
    3.
    发明申请
    MACROLIDES DERIVATIVES AS ANTIBACTERIAL AGENTS 审中-公开
    抗坏血酸衍生物作为抗菌剂

    公开(公告)号:US20090130225A1

    公开(公告)日:2009-05-21

    申请号:US12094800

    申请日:2006-11-21

    CPC分类号: C07H17/08

    摘要: The present invention provides macrolide derivatives, which can be used as antibacterial agents. Compounds described herein can be used for treating or preventing conditions caused by or contributed to by gram-positive, gram-negative or anaerobic bacteria, more particularly against, for example, Staphylococci, Streptococci, Enterococci, Haemophilus, Moraxalla spp., Chlamydia spp., Mycoplasm, Legionella spp., Mycobacterium, Helicobacter, Clostridium, Bacteroides, Corynebacterium, Propionibeacterium, Bacillus, Enterobactericeae or any combination thereof. Also provided are processes for preparing compounds described herein, pharmaceutical compositions thereof, and methods of treating bacterial infections.

    摘要翻译: 本发明提供可用作抗菌剂的大环内酯衍生物。 本文所述的化合物可用于治疗或预防由革兰氏阳性,革兰氏阴性或厌氧细菌引起或促成的病症,特别是针对例如葡萄球菌,链球菌,肠球菌,嗜血杆菌,马克拉斯氏菌属,衣原体属。 ,支原体属,军团菌属,分枝杆菌属,幽门螺杆菌属,梭菌属,拟杆菌属,棒状杆菌属,丙酸杆菌属,芽孢杆菌属,肠杆菌属或其任何组合。 还提供了制备本文所述化合物的方法,其药物组合物和治疗细菌感染的方法。

    Use of Macrolide Derivatives for Treating Acne
    7.
    发明申请
    Use of Macrolide Derivatives for Treating Acne 审中-公开
    使用大环内酯衍生物治疗痤疮

    公开(公告)号:US20090075916A1

    公开(公告)日:2009-03-19

    申请号:US12094645

    申请日:2006-11-22

    IPC分类号: A61K31/7048 A61P17/10

    CPC分类号: A61K31/7056

    摘要: This invention relates to 14-membered macrolide derivatives for treating or preventing acne vulgaris and associated inflammatory conditions. Also provided herein are medicaments or pharmaceutical compositions comprising one or more 14-membered macrolide derivatives together with one or more pharmaceutically acceptable carriers, excipients, diluents or mixture thereof, and methods for treating or preventing acne vulgaris and associated inflammatory conditions.

    摘要翻译: 本发明涉及用于治疗或预防寻常痤疮和相关炎性病症的14-元大环内酯衍生物。 本文还提供包含一种或多种14-元大环内酯衍生物以及一种或多种药学上可接受的载体,赋形剂,稀释剂或其混合物的药物或药物组合物,以及治疗或预防寻常痤疮和相关炎性病症的方法。

    NITROGEN-BASED LINKERS FOR ATTACHING MODIFYING GROUPS TO POLYPEPTIDES AND OTHER MACROMOLECULES
    10.
    发明申请
    NITROGEN-BASED LINKERS FOR ATTACHING MODIFYING GROUPS TO POLYPEPTIDES AND OTHER MACROMOLECULES 有权
    用于连接改性聚氨酯和其他大分子的基于氮的连接

    公开(公告)号:US20090048147A1

    公开(公告)日:2009-02-19

    申请号:US12022926

    申请日:2008-01-30

    摘要: The present invention relates to a compound comprising a peptide moiety, a linker moiety and a water-soluble polymer moiety such as a poly(ethylene glycol) moiety. The linker moiety is between the peptide moiety and the water-soluble polymer moiety. In certain embodiments, the linker moiety has the structure: wherein α, β, and γ are each integers whose values are independently selected. In other embodiments the linker moiety has the following structure: wherein κ, ρ, and τ are each integers whose values are independently selected. In other embodiments the linker moiety has the following structure: wherein χ, φ, γ, and η are each integers whose values are independently selected. Alternatively, the linker structure may have the following structure: wherein λ and μ are each integers whose values are independently selected.

    摘要翻译: 本发明涉及包含肽部分,接头部分和水溶性聚合物部分如聚(乙二醇)部分的化合物。 接头部分在肽部分和水溶性聚合物部分之间。 在某些实施方案中,接头部分具有以下结构:其中α,β和γ各自是其值被独立选择的整数。 在其它实施方案中,接头部分具有以下结构:其中kappa,rho和tau各自是其值被独立选择的整数。 在其它实施方案中,接头部分具有以下结构:其中chi,phi,γ和eta各自是其值被独立选择的整数。 或者,连接体结构可以具有以下结构:其中λ和mu各自是其值被独立选择的整数。