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ANTI-TUMOR-THERMAL TERPENOID PHARMACEUTICAL COMPOSITION WITH ANGIOGENESING-INHIBATING ACTION

机译:具有促血管生成作用的抗肿瘤热萜类药物组合物

摘要

The invention relates to medicine and the pharmaceutical industry and relates to an agent for treating diseases associated with impaired regulation of angiogenesis, in particular to a method for treating oncological diseases of various origins, by inducing inhibition of angiogenesis against a background of direct antitumor, antirecurrent and antimetastatic effects, as well as concomitant activation endogenous apoptosis system. The invention is implemented using a new oral dosage form - Abisilin, containing ingredients belonging to the class of natural terpene compounds (isoprenoids) obtained from conifers of the Pinaceae family, including: sequiterpenoids (3-6%), neutral diterpenoids (11-15%), diterpenic acids (23-28%), triterpenic acids (8-16%), unsaturated and saturated fatty acids (0.1-0.3%), phenolic compounds (0.1-0.2%) and the rest are monoterpenoids, with a content of boron acetate of at least 10.0% of the total composition of terpenes. It is assumed that the use of the new oral dosage form Abisilin, for the substance of which immunomodulating, antibacterial, anti-inflammatory, analgesic, wound healing and other pharmacologically significant actions are known, as well as the absence of contraindications, toxic effects and the possibility of complex use with various agents, implements a new therapeutic approach and will increase the effectiveness treatment of cancer and many other diseases associated with the violation of the processes of angiogenesis.
机译:本发明涉及药物和制药工业,并且涉及一种治疗与血管新生调节不良有关的疾病的药剂,特别是涉及一种通过在直接抗肿瘤,抗复发的背景下诱导血管新生抑制作用来治疗各种起源的肿瘤疾病的方法。和抗转移作用,以及伴随的激活内源性细胞凋亡系统。本发明使用新的口服剂型阿比西林(Abisilin)实施,其中含有从松科科的针叶树中获得的属于天然萜类化合物(异戊二烯类)的成分,包括:半萜类化合物(3-6%),中性二萜类化合物(11-15) %),二萜酸(23-28%),三萜酸(8-16%),不饱和和饱和脂肪酸(0.1-0.3%),酚类化合物(0.1-0.2%),其余为单萜类,含量乙酸硼占萜烯总组成的至少10.0%。假定使用新的口服剂型Abisilin,已知该物质具有免疫调节,抗菌,消炎,镇痛,伤口愈合和其他药理学显着作用,并且没有禁忌症,毒性作用和与各种药物复合使用的可能性,将实施一种新的治疗方法,并将提高对癌症和许多其他与违反血管生成过程有关的疾病的治疗效果。

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