FIELD: medicine, pharmaceutics.
SUBSTANCE: invention refers to compounds of formula (I) where R1 is chosen from a group consisting of phenyl, unsubstituted or substituted by one or two groups independently chosen from (lower) alkyl, (lower) phenylalkyl wherein a phenyl ring can be unsubstituted or substituted by one or two groups independently chosen from halogen; R2 represents hydrogen; or R1 and R2 together with nitrogen atom whereto attached, form a saturated 5- or 6-members heterocyclic ring optionally containing an additional oxygen heteroatom, said saturated heterocyclic ring is unsubstituted or substituted by one, two or three groups independently chosen from (lower) alkyl, halogen; R3 is chosen from a group consisting of hydrogen, (lower) alkyl, (lower) hydroxyalkyl, (lower) alkoxyalkyl, (lower) haloalkyl, (lower) cycloalkylalkyl, (lower) cyanoalkyl, (lower) alkylsulfonyl, phenyl unsubstituted or substituted by one or two groups independently chosen from halogen; R4 represents hydrogen or halogen; R5 represents a group chosen from where m represents 0 or 1; n represents 0,1 or 2; X represents CR13R13'; R6, R6', R7, R7', R8,R8', R13, R13' are independently chosen from a group consisting of hydrogen, (lower) alkyl, halogen; p represents 0 or 1; R9 is chosen from (lower) alkyl, cycloalkyl, (lower) cycloalkylalkyl; q represents 0 or 1; R10 represents (lower) alkyl; and to their pharmaceutically acceptable salts, as well as to a pharmaceutical composition exhibiting histamine 3 receptor antagonistic and/or antagonistic activity and based on the compounds of formula I.
EFFECT: there are prepared and described new compounds which can be effective in treatment and/or prevention of the diseases associated with H3 receptor modulation.
24 cl, 34 ex
Title | Year | Author | Number |
---|---|---|---|
NAPHTHALENE DERIVATIVES SUITABLE FOR USE AS LIGANDS OF HISTAMINE 3 RECEPTORS | 2005 |
|
RU2387638C2 |
INDOLE DERIVATIVES AS HISTAMINE RECEPTOR ANTAGONISTS | 2005 |
|
RU2382778C2 |
QUINOLINE DERIVATIVES | 2005 |
|
RU2391338C2 |
HETEROCYCLIC SUBSTITUTED PHENYLMETHANONES AS GLYCINE TRANSPORTER 1 INHIBITORS | 2006 |
|
RU2405771C2 |
DERIVATIVES OF 1,1-DIOXOTHIOMORPHOLINYLINDOLYL METHANONE FOR USE AS HISTAMINASE MODULATORS | 2006 |
|
RU2412182C2 |
NOVEL PIPERIDINE DERIVATIVES | 2006 |
|
RU2417985C2 |
QUINAZOLINE DERIVATIVES, METHOD FOR THEIR PREPARING AND PHARMACEUTICAL COMPOSITION | 2001 |
|
RU2267489C2 |
PYROLLO [2,3-B]PYRIDINE DERIVATIVES AS PROTEIN KINASE INHIBITORS | 2012 |
|
RU2629999C2 |
PYRROLO[2,3-b]PYRIDINE DERIVATIVES AS PROTEIN KINASE INHIBITORS | 2006 |
|
RU2565071C2 |
BENZODIAZEPINE COMPOUND AND PHARMACEUTICAL COMPOSITION | 2009 |
|
RU2496775C2 |
Authors
Dates
2011-04-27—Published
2006-11-08—Filed