FIELD: pharmaceuticals.
SUBSTANCE: group of inventions relates to a compound selected from compounds of formula I:
and their pharmaceutically acceptable salts, refers to a pharmaceutical composition useful for targeting the spliceosome and mutation therein, containing an effective amount of the compound and/or a pharmaceutically acceptable salt thereof and a pharmaceutically acceptable carrier, also relates to the use of a compound and/or a pharmaceutically acceptable salt thereof or a pharmaceutical composition for the preparation of a medicinal products for the treatment of cancer selected from the following group: myelodysplastic syndrome, chronic lymphocytic leukemia, chronic myelomonocytic leukemia, acute myeloid leukemia, colon cancer, pancreatic cancer, endometrial cancer, ovarian cancer, breast cancer, uveal melanoma, cancer stomach, cholangiocarcinoma and lung cancer.
EFFECT: group of inventions provides for the development of a medicinal product having the structure of a compound of formula I and a targeted effect on the spliceosome.
26 cl, 15 tbl, 205 ex
Title | Year | Author | Number |
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PLADIENOLIDE DERIVATIVES AS DRUGS WITH TARGETED INFLUENCE ON SPLICEOSOME FOR TREATMENT OF CANCER | 2019 |
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SPLICEOSTATIN ANALOGS | 2013 |
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PYRIDINE COMPOUNDS OF PLADIENOLIDE AND METHODS OF THEIR USE | 2015 |
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COMPOUNDS WITH CONDENSED RINGS | 2019 |
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SUBSTITUTED CARBONUCLEOSIDES DERIVATIVES USED AS ANTICANCER AGENTS | 2017 |
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RU2712944C1 |
DERIVATIVES OF CYCLOHEXANE OR TETRAHYDROPYRANE OR THEIR PHARMACEUTICALLY ACCEPTABLE SALTS, OR HYDRATES, OR SOLVATES OF THESE COMPOUNDS, OR THEIR SALTS, INTERMEDIATE COMPOUNDS FOR THEIR SYNTHESIS AND FUNGICIDE AGENT | 1992 |
|
RU2084439C1 |
COMPOSITIONS AND METHODS FOR INHIBITING VIRAL POLYMERASE | 2013 |
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RU2654482C2 |
Authors
Dates
2024-02-13—Published
2019-04-08—Filed