FIELD: chemistry.
SUBSTANCE: invention relates to novel 3,4-dihydrobenzoxazine compounds of general formula [1] (where X denotes a nitrogen atom or CR3; R1 denotes a hydrogen atom or a halogen atom; R2 denotes a C1-6alkoxy group which can be substituted with 1-5 identical or different substitutes selected from a halogen atom and a hydroxyl group; and R3 denotes a halogen atom. However, R1 denotes a halogen atom when X denotes CR3). Said compounds are effective when treating diseases where activity of vanilloid receptors subtype 1 (VR1) is involved, e.g. pain.
EFFECT: more efficient use of pharmaceutical compositions based on said compounds, more effective treatment or pain killing.
19 cl, 4 tbl, 10 ex
Title | Year | Author | Number |
---|---|---|---|
CONDENSED BENZAMIDE DERIVATIVE AND INHIBITOR OF VANILLOID RECEPTOR TYPE 1 ACTIVITY (VRI) | 2005 |
|
RU2392278C2 |
PRODRUGS OF PYRIDONAMIDES USED AS MODULATORS OF SODIUM CHANNELS | 2014 |
|
RU2692766C1 |
NOVEL SPIRO[IMIDAZOLIDINE-4,3'-INDOLE]-2,2',5(1'H)-TRIONES FOR TREATING CONDITIONS ASSOCIATED WITH VANILLOID RECEPTOR 1 | 2007 |
|
RU2421457C2 |
TETRAHYDROQUINOLINE DERIVATIVES AS P2X7 RECEPTOR ANTAGONISTS | 2018 |
|
RU2724350C1 |
AMIDES OF CONDENSED PIPERIDINE AS MODULATORS OF ION CHANNELS | 2014 |
|
RU2741810C2 |
HETEROCYCLIC DERIVATIVES AND USE THEREOF | 2015 |
|
RU2711502C2 |
PYRIDONAMIDE PRODRUGS USED AS SODIUM CHANNELS MODULATORS | 2014 |
|
RU2811402C2 |
SPIROCYCLIC PYRROLOPYRAZINE(PIPERIDINE)AMIDES AS IONIC CHANNELS MODULATORS | 2012 |
|
RU2634900C2 |
HETEROCYCLIC MUSCARINIC AGONISTS AND COMPOSITIONS, THEIR USING AND METHODS FOR TREATMENT | 2002 |
|
RU2292346C2 |
DERIVATIVES OF 3-(6-CHLORO-3-OXO-3.4-DIHYDRO-(2H)-1.4-BENZOXASIN-4-YL)PROPIONIC ACID AND THEIR USE AS KMO INHIBITORS | 2016 |
|
RU2746001C2 |
Authors
Dates
2011-08-27—Published
2006-12-22—Filed