FIELD: chemistry.
SUBSTANCE: compounds of formula (I) can be efficient with respect to diseases, in which phosphorylation of Tau protein takes place. , R3 stands for CONR1R2, where R1 and R2 can be substituted with heterocycle; R5, R6, R7 independently on each other are selected from halogen and phenyl; R1, R2 independently on each other stand for hydrogen, (C1-C6)alkyl or together with nitrogen of group CONR1R can form heterocycle.
EFFECT: obtaining novel biologically active compounds.
4 cl, 3 ex
Title | Year | Author | Number |
---|---|---|---|
NOVEL AMINOINDAZOLE DERIVATIVES AS MEDICINAL AGENTS AND PHARMECEUTICAL COMPOSITIONS CONTAINING SAID DERIVATIVES | 2003 |
|
RU2378259C2 |
AMINOINDAZOLE DERIVATIVES AS MEDICATIONS, METHOD OF THEIR OBTAINING AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM | 2003 |
|
RU2345070C2 |
COMBINATIONS OF ACTIVATOR (ACTIVATORS) OF PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR (PPAR), AND INHIBITOR (INHIBITORS) OF STEROL ABSORPTION AND TREATMENT OF VASCULAR DISEASES | 2008 |
|
RU2483724C2 |
TRIAZINE, PYRIMIDINE AND PYRIDINE ANALOGUES AND USE THEREOF AS THERAPEUTIC AGENTS AND DIAGNOSTIC SAMPLES | 2009 |
|
RU2537945C2 |
METHOD OF SYNTHESISING SULFONYLHALOGENIDES AND SULFONAMIDES FROM SALTS OF SULFONIC ACIDS | 2006 |
|
RU2466983C2 |
N3-ALKYLATED BENZIMIDAZOLE DERIVATIVES AS MEK INHIBITORS | 2003 |
|
RU2300528C2 |
HETEROCYCLIC SUBSTITUTED PHENYLMETHANONES AS GLYCINE TRANSPORTER 1 INHIBITORS | 2006 |
|
RU2405771C2 |
N-ALKYLATED BENZIMIDAZOLE DERIVATIVES AS MEK INHIBITOR | 2003 |
|
RU2307831C9 |
17β-HSD1 AND STS INHIBITORS | 2006 |
|
RU2412196C2 |
PYRROLO[2,3-B]PYRIDINE DERIVATIVE AS PROTEIN KINASE INHIBITORS | 2006 |
|
RU2418800C2 |
Authors
Dates
2008-11-27—Published
2003-09-03—Filed