FIELD: medicine; pharmaceuticals.
SUBSTANCE: invention relates to taxane compounds having a structure represented by the following general formula I:
where R1 is benzoyl, tert-butyloxycarbonyl or N,N'-dimethylcarbamoyl; R2 is phenyl, or R3 is -OMe, -OOCOC3, -OCON (CH3)2 or -OCOSC2H5; R4 is -OMe, -OOCOC3, -OCON (CH3)2, -OCOSC2H5 or H, wherein R3 and R4 do not represent -OM simultaneously; or their pharmaceutically acceptable non-toxic salts or isomers. Also disclosed are taxane compounds of formula II, an anti-tumor pharmaceutical composition, use of taxane compounds and a composition, a method of producing taxane compounds.
EFFECT: disclosed taxane compounds have improved oral bioavailability and are characterized by strong cytotoxicity with respect to a number of human cancer cell lines and broad spectrum anti-tumor effects.
10 cl, 67 dwg, 23 ex, 6 tbl
Title | Year | Author | Number |
---|---|---|---|
TAXANIC COMPOUND, AS WELL AS PREPARATION METHOD AND USE THEREOF | 2014 |
|
RU2686459C1 |
ERBB RECEPTOR INHIBITORS | 2019 |
|
RU2810215C2 |
PYRIDAZINE DERIVATIVES AS RORc MODULATORS | 2017 |
|
RU2757571C2 |
DERIVATIVE BASED ON DIHYDROPYRIMIDO-RING AS HBV INHIBITOR | 2015 |
|
RU2693897C2 |
ARGINASE INHIBITORS AND THERAPEUTIC USE THEREOF | 2011 |
|
RU2586219C2 |
SUBSTITUTED INDOLE COMPOUNDS AS REDUCING REGULATORS OF ESTROGEN RECEPTORS | 2017 |
|
RU2722441C2 |
SPLICEOSTATIN ANALOGS | 2013 |
|
RU2618523C2 |
SYNTHESIS OF CARBAMOYL PYRIDONE INHIBITORS OF HIV INTEGRASE AND INTERMEDIATE COMPOUNDS | 2009 |
|
RU2527451C2 |
SYNTHESIS OF CARBAMOIL-PYRIDONE INHIBITORS OF HIV INTEGRASE AND INTERMEDIATE COMPOUNDS | 2013 |
|
RU2638923C2 |
ISOINDOLINE COMPOUND, PRODUCTION METHOD, PHARMACEUTICAL COMPOSITION AND THEIR USE | 2019 |
|
RU2813232C2 |
Authors
Dates
2019-04-30—Published
2014-11-21—Filed