(THIO) CARBAMOYL-CYCLOHEXANE DERIVATIVES AS D3/D2 RECEPTOR ANTAGONISTS

Predstavljeni pronalazak se odnosi na nove ligande za podgrupu D2 i D3 dopaminskih receptora formule (I): gdje R1 i R2 nezavisno predstavljaju supsti tuent izabran iz grupe koju čine vodonik, alkil, aril, cikloalkil, aroil, ili R1 i R2 mogu da formiraju heterocikličan prsten sa susjednim atomom azot...

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Main Authors VAGO, ISTVAN, AGAINE CSONGOR, EVA, KISS, BELA, LASZY, JUDIT, LASZLOVSZKY, ISTVAN, SAGHY, KATALIN, GALAMBOS, JANOS, GYERTYAN, ISTVAN, NOGRADI, KATALIN
Format Patent
LanguageCroatian
English
Published 20.12.2011
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Abstract Predstavljeni pronalazak se odnosi na nove ligande za podgrupu D2 i D3 dopaminskih receptora formule (I): gdje R1 i R2 nezavisno predstavljaju supsti tuent izabran iz grupe koju čine vodonik, alkil, aril, cikloalkil, aroil, ili R1 i R2 mogu da formiraju heterocikličan prsten sa susjednim atomom azota; X predstavlja atom kiseonika ili sumpora; n je cio broj od 1 do 2; i/ili njihove geometrijske izomere i/ili stereoizomere i/ili diastereomere i/ili soli i/ili hidrate i/ili solvate, na postupak za njihovu proizvodnju, farmaceutske kompozicije koje ih sadrže i na njihovu primjenu u liječenju i/ili prevencijui stanja koje zahti jeva modulaciju dopaminskih receptora. The present invention relates to new D3 and D2 dopamine receptor subtype preferring ligands of formula (I): wherein R1 and R2 represent independently a substituent selected from hydrogen, alkyl, aryl, cycloalkyl, aroyl, or R1 and R2 may form a heterocyclic ring with the adjacent nitrogen atom; X represents an oxygen or sulphur atom; n is an integer of from 1 to 2, and/or geometric isomers and/or stereoisomers and/or diastereomers and/or salts and/or hydrates and/or solvates thereof, to the processes for producing the same, to pharmaceutical compositions containing the same and to their use in therapy and/or prevention of a condition which requires modulation of dopamine receptors.
AbstractList Predstavljeni pronalazak se odnosi na nove ligande za podgrupu D2 i D3 dopaminskih receptora formule (I): gdje R1 i R2 nezavisno predstavljaju supsti tuent izabran iz grupe koju čine vodonik, alkil, aril, cikloalkil, aroil, ili R1 i R2 mogu da formiraju heterocikličan prsten sa susjednim atomom azota; X predstavlja atom kiseonika ili sumpora; n je cio broj od 1 do 2; i/ili njihove geometrijske izomere i/ili stereoizomere i/ili diastereomere i/ili soli i/ili hidrate i/ili solvate, na postupak za njihovu proizvodnju, farmaceutske kompozicije koje ih sadrže i na njihovu primjenu u liječenju i/ili prevencijui stanja koje zahti jeva modulaciju dopaminskih receptora. The present invention relates to new D3 and D2 dopamine receptor subtype preferring ligands of formula (I): wherein R1 and R2 represent independently a substituent selected from hydrogen, alkyl, aryl, cycloalkyl, aroyl, or R1 and R2 may form a heterocyclic ring with the adjacent nitrogen atom; X represents an oxygen or sulphur atom; n is an integer of from 1 to 2, and/or geometric isomers and/or stereoisomers and/or diastereomers and/or salts and/or hydrates and/or solvates thereof, to the processes for producing the same, to pharmaceutical compositions containing the same and to their use in therapy and/or prevention of a condition which requires modulation of dopamine receptors.
Author VAGO, ISTVAN
SAGHY, KATALIN
NOGRADI, KATALIN
GYERTYAN, ISTVAN
AGAINE CSONGOR, EVA
GALAMBOS, JANOS
LASZLOVSZKY, ISTVAN
LASZY, JUDIT
KISS, BELA
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– fullname: LASZY, JUDIT
– fullname: LASZLOVSZKY, ISTVAN
– fullname: SAGHY, KATALIN
– fullname: GALAMBOS, JANOS
– fullname: GYERTYAN, ISTVAN
– fullname: NOGRADI, KATALIN
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Snippet Predstavljeni pronalazak se odnosi na nove ligande za podgrupu D2 i D3 dopaminskih receptora formule (I): gdje R1 i R2 nezavisno predstavljaju supsti tuent...
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SubjectTerms CHEMISTRY
HETEROCYCLIC COMPOUNDS
HUMAN NECESSITIES
HYGIENE
MEDICAL OR VETERINARY SCIENCE
METALLURGY
ORGANIC CHEMISTRY
PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS
Title (THIO) CARBAMOYL-CYCLOHEXANE DERIVATIVES AS D3/D2 RECEPTOR ANTAGONISTS
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