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Results: 1-14 |
Results: 14
A SEARCH FOR NEW 5-HT1A 5-HT2A RECEPTOR LIGANDS - IN-VITRO AND IN-VIVO STUDIES OF GA-(4-ARYL-1-PIPERAZINYL)ALKYL]INDOLIN-2(1H)-ONES/
Authors: MOKROSZ MJ DUSZYNSKA B MISZTAL S KLODZINSKA A TATARCZYNSKA E CHOJNACKAWOJCIK E DZIEDZICKAWASYLEWSKA M
Citation: Mj. Mokrosz et al., A SEARCH FOR NEW 5-HT1A 5-HT2A RECEPTOR LIGANDS - IN-VITRO AND IN-VIVO STUDIES OF GA-(4-ARYL-1-PIPERAZINYL)ALKYL]INDOLIN-2(1H)-ONES/, Archiv der pharmazie, 331(10), 1998, pp. 325-330
4-(3-FURYL)-2-(4-METHYLPIPERAZINO)PYRIMIDINES - POTENT 5-HT2A RECEPTOR ANTAGONISTS
Authors: MOKROSZ MJ DUSZYNSKA B KLODZINSKA A DERENWESOLEK A CHOJNACKAWOJCIK E BARANOWSKI TC ABDOU IM REDMORE NP STREKOWSKI L
Citation: Mj. Mokrosz et al., 4-(3-FURYL)-2-(4-METHYLPIPERAZINO)PYRIMIDINES - POTENT 5-HT2A RECEPTOR ANTAGONISTS, Bioorganic & medicinal chemistry letters, 7(13), 1997, pp. 1635-1638
5-HT1A AND 5-HT2A RECEPTOR AFFINITY AND FUNCTIONAL PROFILE OF SOME N-[3-(4-ARYL-1-PIPERAZINYL)PROPYL] DERIVATIVES OF INDOLIN-2(1H)-ONE, QUINOLIN-2(1H)ONE AND ISOQUINOLIN-1(2H)-ONE .30. STRUCTURE-ACTIVITY RELATIONSHIP STUDIES OF CNS AGENTS
Authors: MOKROSZ MJ MOKROSZ JL DUSZYNSKA B DERENWESOLEK A KLODZINSKA A KOWALSKI P CHARAKCHIEVAMINOL S TATARCZYNSKA E KOWALSKA T MAJKA Z CHOJNACKAWOJCIK E MISZTAL S
Citation: Mj. Mokrosz et al., 5-HT1A AND 5-HT2A RECEPTOR AFFINITY AND FUNCTIONAL PROFILE OF SOME N-[3-(4-ARYL-1-PIPERAZINYL)PROPYL] DERIVATIVES OF INDOLIN-2(1H)-ONE, QUINOLIN-2(1H)ONE AND ISOQUINOLIN-1(2H)-ONE .30. STRUCTURE-ACTIVITY RELATIONSHIP STUDIES OF CNS AGENTS, Die Pharmazie, 52(6), 1997, pp. 423-428
3-(OMEGA-AMINOALKYL)-5,5-DIALKYL (OR SPIROCYCLOALKYL-1',5-)HYDANTOINSAS NEW 5-HT1A AND 5-HT2A RECEPTOR LIGANDS
Authors: BYRTUS H PAWLOWSKI M CHARAKCHIEVAMINOL S DUSZYNSKA B MOKROSZ MJ MOKROSZ JL ZEJC A
Citation: H. Byrtus et al., 3-(OMEGA-AMINOALKYL)-5,5-DIALKYL (OR SPIROCYCLOALKYL-1',5-)HYDANTOINSAS NEW 5-HT1A AND 5-HT2A RECEPTOR LIGANDS, Archiv der pharmazie, 329(6), 1996, pp. 283-290
STRUCTURE-ACTIVITY RELATIONSHIP STUDIES OF CNS AGENTS .29. N-METHYLPIPERAZINO-SUBSTITUTED DERIVATIVES OF QUINAZOLINE, PHTHALAZINE AND QUINOLINE AS NOVEL ALPHA(1), 5-HT1A AND 5-HT2A RECEPTOR LIGANDS
Authors: MOKROSZ JL DUSZYNSKA B CHARAKCHIEVAMINOL S BOJARSKI AJ MOKROSZ MJ WYDRA RL JANDA L STREKOWSKI L
Citation: Jl. Mokrosz et al., STRUCTURE-ACTIVITY RELATIONSHIP STUDIES OF CNS AGENTS .29. N-METHYLPIPERAZINO-SUBSTITUTED DERIVATIVES OF QUINAZOLINE, PHTHALAZINE AND QUINOLINE AS NOVEL ALPHA(1), 5-HT1A AND 5-HT2A RECEPTOR LIGANDS, European journal of medicinal chemistry, 31(12), 1996, pp. 973-980
QUINOLINYL)]BUTYL]-8-AZASPIRO[4,5]DECANE-7,9-DIONE - A NEW 5-HT1A RECEPTOR-LIGAND WITH THE SAME ACTIVITY PROFILE AS BUSPIRONE
Authors: MOKROSZ JL DERENWESOLEK A TATARCZYNSKA E DUSZYNSKA B BOJARSKI AJ MOKROSZ MJ CHOJNACKAWOJCIK E
Citation: Jl. Mokrosz et al., QUINOLINYL)]BUTYL]-8-AZASPIRO[4,5]DECANE-7,9-DIONE - A NEW 5-HT1A RECEPTOR-LIGAND WITH THE SAME ACTIVITY PROFILE AS BUSPIRONE, Journal of medicinal chemistry, 39(5), 1996, pp. 1125-1129
6-DI(HETEROARYL)-2-(N-METHYLPIPERAZINO)PYRIMIDINES AS NEW, POTENT 5-HT2A RECEPTOR LIGANDS - A VERIFICATION OF THE TOPOGRAPHIC MODEL
Authors: MOKROZ MJ STREKOWSKI L KOZAK WX DUSZYNSKA B BOJARSKI AJ KLODZINSKA A CZARNY A CEGLA MT DERENWESOLEK A CHOHNACKAWOJCIK E DOVE S MOKROSZ JL
Citation: Mj. Mokroz et al., 6-DI(HETEROARYL)-2-(N-METHYLPIPERAZINO)PYRIMIDINES AS NEW, POTENT 5-HT2A RECEPTOR LIGANDS - A VERIFICATION OF THE TOPOGRAPHIC MODEL, Archiv der pharmazie, 328(9), 1995, pp. 659-666
STRUCTURE-ACTIVITY RELATIONSHIP STUDIES OF CNS AGENTS .23. N-(3-PHENYLPROPYL)-1,2,3,4-TETRAHYDRO-ISOQUINOLINE AND N-[(E)-CINNAMYL]-1,2,3,4-TETRAHYDRO-ISOQUINOLINE MIMIC 1-PHENYLPIPERAZINE AT 5-HT1A RECEPTORS
Authors: MOKROSZ JL BOJARSKI AJ CHARAKCHIEVAMINOL S DUSZYNSKA B MOKROSZ MJ PALUCHOWSKA MH
Citation: Jl. Mokrosz et al., STRUCTURE-ACTIVITY RELATIONSHIP STUDIES OF CNS AGENTS .23. N-(3-PHENYLPROPYL)-1,2,3,4-TETRAHYDRO-ISOQUINOLINE AND N-[(E)-CINNAMYL]-1,2,3,4-TETRAHYDRO-ISOQUINOLINE MIMIC 1-PHENYLPIPERAZINE AT 5-HT1A RECEPTORS, Archiv der pharmazie, 328(7-8), 1995, pp. 604-608
STRUCTURE-ACTIVITY RELATIONSHIP STUDIES OF CNS AGENTS .22. A SEARCH FOR NEW TRAZODONE-LIKE ANTIDEPRESSANTS - SYNTHESIS AND PRELIMINARY RECEPTOR-BINDING STUDIES
Authors: MOKROSZ JL DUSZYNSKA B PALUCHOWSKA MH CHARAKCHIEVAMINOL S MOKROSZ MJ
Citation: Jl. Mokrosz et al., STRUCTURE-ACTIVITY RELATIONSHIP STUDIES OF CNS AGENTS .22. A SEARCH FOR NEW TRAZODONE-LIKE ANTIDEPRESSANTS - SYNTHESIS AND PRELIMINARY RECEPTOR-BINDING STUDIES, Archiv der pharmazie, 328(7-8), 1995, pp. 623-625
STRUCTURE-ACTIVITY RELATIONSHIP STUDIES OF CNS AGENTS .22. 2 DERIVATIVES OF 1-(O-METHOXYPHENYL)PIPERAZINE WITH AN OPPOSITE FUNCTION AT 5-HT1A RECEPTORS
Authors: MOKROSZ JL KLODZINSKA A BOKSA J BOJARSKI AJ DUSZYNSKA B CHOJNACKAWOJCIK E
Citation: Jl. Mokrosz et al., STRUCTURE-ACTIVITY RELATIONSHIP STUDIES OF CNS AGENTS .22. 2 DERIVATIVES OF 1-(O-METHOXYPHENYL)PIPERAZINE WITH AN OPPOSITE FUNCTION AT 5-HT1A RECEPTORS, Archiv der pharmazie, 328(4), 1995, pp. 381-383
STRUCTURE-ACTIVITY RELATIONSHIP STUDIES OF CNS AGENTS .19. QUANTITATIVE-ANALYSIS OF THE ALKYL CHAIN EFFECTS ON THE 5-HT1A AND 5-HT2 RECEPTOR AFFINITIES OF 4-ALKYL-1-ARYLPIPERAZINES AND THEIR ANALOGS
Authors: MOKROSZ JL MOKROSZ MJ CHARAKCHIEVAMINOL S PALUCHOWSKA MH BOJARSKI AJ DUSZYNSKA B
Citation: Jl. Mokrosz et al., STRUCTURE-ACTIVITY RELATIONSHIP STUDIES OF CNS AGENTS .19. QUANTITATIVE-ANALYSIS OF THE ALKYL CHAIN EFFECTS ON THE 5-HT1A AND 5-HT2 RECEPTOR AFFINITIES OF 4-ALKYL-1-ARYLPIPERAZINES AND THEIR ANALOGS, Archiv der pharmazie, 328(2), 1995, pp. 143-148
STRUCTURE-ACTIVITY RELATIONSHIP STUDIES OF CNS AGENTS .20. PERAZINYL]ALKYL]1,2,3,4-TETRAHYDRO-BETA-CARBOLINES - NEW 5-HT1A AND 5-HT2A RECEPTOR LIGANDS
Authors: BOKSA J DUSZYNSKA B MOKROSZ JL
Citation: J. Boksa et al., STRUCTURE-ACTIVITY RELATIONSHIP STUDIES OF CNS AGENTS .20. PERAZINYL]ALKYL]1,2,3,4-TETRAHYDRO-BETA-CARBOLINES - NEW 5-HT1A AND 5-HT2A RECEPTOR LIGANDS, Die Pharmazie, 50(3), 1995, pp. 220-221
STRUCTURE-ACTIVITY RELATIONSHIP STUDIES OF CNS AGENTS .15. ERAZINYL)ALKYL]-2-OXO-1,2,3,4-TETRAHYDROQUINOLINES AND YL]-4-OXO-1,2,3,4-TETRAHYDROPYRAZINO[1,2-A]INDOLES - NEW, HIGHLY POTENT 5-HT1A LIGANDS
Authors: MOKROSZ JL DUSZYNSKA B PALUCHOWSKA MH
Citation: Jl. Mokrosz et al., STRUCTURE-ACTIVITY RELATIONSHIP STUDIES OF CNS AGENTS .15. ERAZINYL)ALKYL]-2-OXO-1,2,3,4-TETRAHYDROQUINOLINES AND YL]-4-OXO-1,2,3,4-TETRAHYDROPYRAZINO[1,2-A]INDOLES - NEW, HIGHLY POTENT 5-HT1A LIGANDS, Archiv der pharmazie, 327(8), 1994, pp. 529-531
STRUCTURE-ACTIVITY RELATIONSHIP STUDIES OF CNS AGENTS .14. STRUCTURALREQUIREMENTS FOR THE 5-HT1A AND 5-HT2A RECEPTOR SELECTIVITY OF SIMPLE1-(2-PYRIMIDINYL)PIPERAZINE DERIVATIVES
Authors: MOKROSZ JL STREKOWSKI L DUSZYNSKA B HARDEN DB MOKROSZ MJ BOJARSKI AJ
Citation: Jl. Mokrosz et al., STRUCTURE-ACTIVITY RELATIONSHIP STUDIES OF CNS AGENTS .14. STRUCTURALREQUIREMENTS FOR THE 5-HT1A AND 5-HT2A RECEPTOR SELECTIVITY OF SIMPLE1-(2-PYRIMIDINYL)PIPERAZINE DERIVATIVES, Die Pharmazie, 49(11), 1994, pp. 801-806
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