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Antitumor and anticholesterol formulations containing lipoteichoic acid from Streptococcus

机译:含有链球菌脂蛋白的抗肿瘤和抗胆固醇制剂

摘要

The invention concerns a new lipoteichoic acid which can be isolated from the new Streptococcus sp DSM 8747. The new LTA is called LTA-T. It has a lipid anchor, which is a galacto-furanosyl-beta-1-3-glycerol with different rests of fatty acids esterified in the two adjacent hydroxy groups in the glycerol moiety and a non-glycosylated, linear, unbranched GroP chain with an unusual short hydrophilic GroP chain. The hydrophilic backbone consists of only 10 glycerophosphate units esterified with D-alanine in an extent of 30%. The invention further concerns a pharmaceutical composition with the new LTA-T, optionally together with a monokine and/or hyaluronidase, a method of treating cancer comprising administration of an antitumor effective amount thereof, a method of producing the new compound and the new pharmaceutical composition, two degradation products of the new LTA-T and their use, and the new Streptococcus strain from which the new compound can be isolated.
机译:本发明涉及可以从新的链球菌sp DSM 8747分离的新的脂磷壁酸。新的LTA被称为LTA-T。它具有脂质锚定物,即半乳糖-呋喃糖基-β-1-3-甘油,在甘油部分的两个相邻羟基中酯化了不同的脂肪酸残基,并且具有非糖基化,线性,无支链的GroP链,具有不寻常的亲水性GroP短链。亲水性骨架仅由10个以D-丙氨酸酯化30%的甘油磷酸酯单元组成。本发明进一步涉及具有新的LTA-T,任选地与单因子和/或透明质酸酶一起的药物组合物,包括抗肿瘤有效量的癌症的治疗方法,新化合物的制备方法和新药物组合物,新LTA-T的两种降解产物及其用途,以及可以从中分离出新化合物的新链球菌菌株。

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