FIELD: organic chemistry, chemical technology, pharmacy. SUBSTANCE: invention describes the novel derivatives of benzofuranone of the general formula (I) where each of R1-R5 means hydrogen atom, hydroxyl-group, direct or branched alkyl, alkylhydroxy- or aralkylhydroxy-group containing 1-7 carbon atoms, halogen atom, amino-group or alkylenedihydroxy-group bound respectively by the point of R1 and R2, R2 and R3, R3 and R4 or R4 and R5, means hydroxyl-group, direct or branched alkoxy- or aralkylhydroxy-group containing 1-7 carbon atoms or carboxylic acid ester residue containing 1-7 carbon atoms. Compounds show inhibiting effect on activity of 17-β--hydroxysteroid dehydrogenase. Invention describes also method of their synthesis and medicinal and therapeutic agent based on thereof. EFFECT: new derivatives indicated above, improved method of synthesis. 5 cl, 8 tbl
Title | Year | Author | Number |
---|---|---|---|
TETRALONE OR BENZOPYRANONE DERIVATIVES, METHOD OF THEIR SYNTHESIS AND DRUG | 1998 |
|
RU2152379C1 |
GLYCOPROTEIN TCF-II AND PHARMACEUTICAL COMPOSITION CONTAINING EFFECTIVE AMOUNT OF GLYCOPROTEIN TCF-II | 1991 |
|
RU2097432C1 |
HETEROCYCLIC COMPOUNDS OR PHARMACEUTICALLY ACCEPTABLE SALT THEREOF AND INTERMEDIATE COMPOUNDS | 1994 |
|
RU2176640C2 |
QUINOLINE DERIVATIVES | 1995 |
|
RU2137770C1 |
HETEROBICYCLIC DERIVATIVES, METHODS OF THEIR SYNTHESIS AND PHARMACEUTICAL COMPOSITION | 1995 |
|
RU2170737C2 |
CYCLOPEPTIDE OR ITS PHARMACEUTICALLY ACCEPTABLE SALT, METHODS OF SYNTHESIS AND PHARMACEUTICAL COMPOSITION | 1991 |
|
RU2108342C1 |
PROTECTIVE AGENT FOR NEURAL RETINA CELLS CONTAINING INDAZOLE DERIVATIVES AS ACTIVE INGREDIENT | 2006 |
|
RU2392938C2 |
CDNA FRAGMENT ENCODING GLYCOPROTEIN TCF-II | 1990 |
|
RU2113480C1 |
AROMATIC AMIDINE DERIVATIVE AND PHARMACEUTICAL COMPOSITION | 1992 |
|
RU2139851C1 |
PYRIDONE CARBOXYLIC ACID DERIVATIVES AND COMPOSITION BASED ON THEREOF | 1993 |
|
RU2100351C1 |
Authors
Dates
2000-07-10—Published
1998-01-13—Filed