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pharmaceutical combination for simultaneous, separate or sequential administration and uses of pharmaceutical combinations and a phosphorylation site inhibitor on ck2 substrates and a pharmaceutically acceptable cytostatic

机译:用于同时,分开或顺序给药的药物组合,以及在ck2底物和药学上可接受的细胞抑制剂中使用药物组合和磷酸化位点抑制剂

摘要

PHARMACEUTICAL COMBINATION FOR SIMULTANEOUS, SEPARATE OR SEQUENTIAL ADMINISTRATION AND USES OF PHARMACEUTICAL COMBINATIONS AND A PHOSPHORILATION SITE INHIBITOR AND A CYPOSTHETIC PHARMACEUTICAL INHIBITOR CASE PRESENTATION A PHARMACEUTICAL INHIBITOR CASE 2 (called P 15) and cytostatics used in cancer chemotherapy which are administered simultaneously, separately or sequentially. Preferred cytostatics are platinum, taxanes, Vinca alkaloids, 5-fluorouracil, doxorubicin, cyclophosphamide, etoposide, mitomycin C, imatinib, iressa and velcade (vortezomib). The synergy between the P 15 peptide and the anticancer chemical compounds means that the effective concentration of each cytostatic in the combination is between one and two orders of magnitude smaller than that of cytostatics alone. Consequently, the combination described in the invention has a much lower toxicity than that reported for anticancer cytostatics which represents a crucial advantage for its use in cancer treatment. In addition, the sequentially administered combination produces chemosensitization of the cytostatic refractory tumors by pretreatment with the P 15 peptide.
机译:用于同时,单独或顺序管理的药物组合,以及用于药物组合的用途,以及用于磷化位阻和药的药物抑制剂的表现形式分别用于癌症的药物抑制剂(第2种,P 15)或化疗,同时使用或抑制细胞的药物抑制剂。优选的细胞抑制剂为铂,紫杉烷,长春花生物碱,5-氟尿嘧啶,阿霉素,环磷酰胺,依托泊苷,丝裂霉素C,伊马替尼,易瑞沙和维卡多(vortezomib)。 P 15肽与抗癌化合物之间的协同作用意味着,每种细胞抑制剂在组​​合中的有效浓度比单独的细胞抑制剂的有效浓度小一到两个数量级。因此,本发明中描述的组合具有比报道的抗癌细胞抑制剂低得多的毒性,这代表了其在癌症治疗中的关键优势。另外,顺序施用的组合通过用P 15肽预处理产生对细胞抑制性难治性肿瘤的化学增敏作用。

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