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    • 7. 发明申请
    • BISACYLOXYPROPYLCYSTEINE CONJUGATES AND THE USE THEREOF
    • 双异丙氧基丙酮共轭物及其用途
    • WO2004009125A3
    • 2004-05-27
    • PCT/EP0307892
    • 2003-07-18
    • BIOTECHNOLOG FORSCHUNG GMBHMUEHLRADT PETERMORR MICHAEL
    • MUEHLRADT PETERMORR MICHAEL
    • A61K47/48
    • A61K47/60
    • The invention relates to novel lipopeptide conjugates, in which a cysteine that is double-substituted by a fatty acid is bonded by means of the carboxyl group to a highly soluble, physiologically compatible and non-immunogenic, polymeric conjugate group. The novel conjugates exhibit an excellent macrophage stimulant action and do not require additional solutizing. They can be used in a wide range of applications, in particular for stimulating macrophages, for stimulating antibody synthesis, for combating infection, as an immunostimulant, in particular in relation to tumours, for preventing and treating septicaemic shock, for wound healing and as an adjuvant for vaccines.
    • 存在其中的双脂肪酸取代的羧基基团的半胱氨酸来提出的新的脂肽缀合物一个易溶于水的和生理上耐受的和非免疫原性聚合物缀合物基团结合。 新的结合物显示非常好的巨噬细胞刺激作用,并且不需要额外的溶解。 它们本身对许多用途,特别是用于刺激巨噬细胞,刺激抗体的合成,用于抗感染防御,用于刺激免疫,特别是抗肿瘤,对于脓毒性休克的预防和治疗,用于伤口愈合,并作为疫苗的佐剂。