Mokrosz JL - Search Results

1

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(1 H)-one and isoquinolin-1(2H)-one. Part 30: Structure-activity relationship studies of CNS agents.

Mokrosz MJ, Mokrosz JL, Duszyńska B, Dereń-Wesołek A, Kłodzińska A, Kowalski P, Charakchieva-Minol S, Tatarczyńska E, Kowalska T, Majka Z, Chojnacka-Wójcik E, Misztal S. Mokrosz MJ, et al. Among authors: mokrosz jl. Pharmazie. 1997 Jun;52(6):423-8. Pharmazie. 1997. PMID: 9260266

2

Structure-activity relationship studies of CNS agents. Part VII. The effect of the imidazole fragment in 2-substituted 1-[3-(4-aryl-1-piperazinyl)propyl]imidazoles on their interaction modes with 5-HT1A and 5-HT2 receptors.

Mokrosz JL, Duszyńska B. Mokrosz JL, et al. Pol J Pharmacol Pharm. 1992 Sep-Oct;44(5):527-38. Pol J Pharmacol Pharm. 1992. PMID: 1297115

3

Structure-activity relationship studies of CNS agents. Part VIII. Bulk tolerance around the protonation center of 4-substituted 1-(3-chlorophenyl)piperazines at 5-HT1A and 5-HT2 receptors.

Mokrosz JL, Charakchieva-Minol S, Paluchowska MH, Cegła MT. Mokrosz JL, et al. Pol J Pharmacol Pharm. 1992 Nov-Dec;44(6):595-607. Pol J Pharmacol Pharm. 1992. PMID: 1305959

4

Structure-activity relationship studies of CNS agents. Part III. On the bioactive conformations of 1-arylpiperazines at 5-HT1A receptor.

Mokrosz JL, Duszyńska B, Bojarski A. Mokrosz JL, et al. Pol J Pharmacol Pharm. 1992 Jan-Feb;44(1):87-97. Pol J Pharmacol Pharm. 1992. PMID: 1359516

5

Structure-activity relationship studies of CNS agents. Part 4: 2-[3-(4-aryl-1-piperazinyl)propyl]-1,2,3,4-tetrahydro-beta-carbolin+ ++ -1-one derivatives as potential central anti-serotonin agents.

Boksa J, Misztal S, Chojnacka-Wójcik E, Gastoł-Lewińska L, Gródecka A, Mokrosz JL. Boksa J, et al. Among authors: mokrosz jl. Pharmazie. 1992 Apr;47(4):254-7. Pharmazie. 1992. PMID: 1518881

6

Structure-activity relationship studies of CNS agents. Part 1: The Free-Wilson analysis of acute toxicity and sedative effect of some 1,2,3,4-tetrahydro-beta-carbolines.

Mokrosz JL, Dukat M, Misztal S, Chojnacka-Wójcik E, Tatarczyńska E. Mokrosz JL, et al. Pharmazie. 1990 Oct;45(10):765-7. Pharmazie. 1990. PMID: 2089388

7

Structure-activity relationship studies of CNS agents, Part 23: N-(3-phenylpropyl)- and N-[(E)-cinnamyl]-1,2,3,4-tetrahydroisoquinoline mimic 1-phenylpiperazine at 5-HT1A receptors.

Mokrosz JL, Bojarski AJ, Charakchieva-Minol S, Duszynska B, Mokrosz MJ, Paluchowska MH. Mokrosz JL, et al. Arch Pharm (Weinheim). 1995 Jul-Aug;328(7-8):604-8. doi: 10.1002/ardp.19953280707. Arch Pharm (Weinheim). 1995. PMID: 7492265

8

Structure-activity relationship studies of CNS agents, Part 22. A search for new trazodone-like antidepressants: synthesis and preliminary receptor binding studies.

Mokrosz JL, Duszynska B, Paluchowska MH, Charakchieva-Minol S, Mokrosz MJ. Mokrosz JL, et al. Arch Pharm (Weinheim). 1995 Jul-Aug;328(7-8):623-5. doi: 10.1002/ardp.19953280711. Arch Pharm (Weinheim). 1995. PMID: 7492269

9

Structure-activity relationship studies of CNS agents. XII. 1-[4-(4-aryl-1-piperazinyl)butyl]-3,4-dihydro-2(1H)-quinolinones: new 5-HT1A, 5-HT2 and D2 ligands with a potential antipsychotic activity.

Mokrosz JL, Chojnacka-Wójcik E, Dereń-Wesołek A, Kłodzińska A, Maćkowiak M, Bielecka Z, Paluchowska MH. Mokrosz JL, et al. Drug Des Discov. 1994 Apr;11(3):197-203. Drug Des Discov. 1994. PMID: 7548635

10

Structure-activity relationship studies of CNS agents, XXI: Two derivatives of 1-(o-methoxyphenyl)piperazine with an opposite function at 5-HT1A receptors.

Mokrosz JL, Klodzinska A, Boksa J, Bojarski AJ, Duszynska B, Chojnacka-Wójcik E. Mokrosz JL, et al. Arch Pharm (Weinheim). 1995 Apr;328(4):381-3. doi: 10.1002/ardp.19953280417. Arch Pharm (Weinheim). 1995. PMID: 7611833 No abstract available.

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