FIELD: pharmaceuticals.
SUBSTANCE: invention relates to a pharmaceutical composition comprising an effective amount of a compound selected from a compound of formulas 1, 2, 3, 4 or a pharmaceutically acceptable salt thereof intended for the treatment of cancer that is sensitive to the action of an agent having splicing inhibitory activity, where the cancer is selected from pulmonary adenocarcinoma (LUAD), uterine endometrial carcinoma (UCEC), massive progressive fibrosis (PMF), prostate adenocarcinoma (PRAD), colon adenocarcinoma (COAD), serous cystadenocarcinoma of the ovary (OV), cutaneous melanoma (SKCM), squamous cell carcinoma lung cell (LUSC), gastric adenocarcinoma (STAD), glioblastoma multiforme (GBM), low-grade brain glioma (LGG) and diffuse B-cell lymphoma (DLBCL), wherein the pharmaceutical composition further contains one or more pharmaceutically acceptable carriers. The invention also relates to the use of compounds of formula 1, 2, 3, 4 for the preparation of the said pharmaceutical composition.
EFFECT: obtaining a pharmaceutical composition that can be used in medicine as an effective agent in the treatment of oncological diseases, in particular oncological diseases for which agents targeting the spliceosome and its mutations are suitable.
15 cl, 10 dwg, 7 tbl
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Authors
Dates
2023-11-13—Published
2015-05-13—Filed