Mokrosz MJ - 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

Novel 4-alkyl-1-arylpiperazines and 1,2,3,4-tetrahydroisoquinolines containing diphenylmethylamino or diphenylmethoxy fragment with differentiated 5-HT1A/5-HT2A/D2 receptor activity.

Paluchowska MH, Mokrosz MJ, Charakchieva-Minol S, Duszyńska B, Kozioł A, Wesołowska A, Stachowicz K, Chojnacka-Wójcik E. Paluchowska MH, et al. Among authors: mokrosz mj. Pol J Pharmacol. 2003 Jul-Aug;55(4):543-52. Pol J Pharmacol. 2003. PMID: 14581712 Free article.

3

Structure-activity relationship studies of CNS agents, Part 25. 4,6-di(heteroaryl)-2-(N-methylpiperazino)pyrimidines as new, potent 5-HT2A receptor ligands: a verification of the topographic model.

Mokrosz MJ, Strekowski L, Kozak WX, Duszyńska B, Bojarski AJ, Kłodzinska A, Czarny A, Cegła MT, Dereń-Wesoøek A, Chojnacka-Wójcik E, et al. Mokrosz MJ, et al. Arch Pharm (Weinheim). 1995 Sep;328(9):659-66. doi: 10.1002/ardp.19953280906. Arch Pharm (Weinheim). 1995. PMID: 7487423

4

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. Among authors: mokrosz mj. Arch Pharm (Weinheim). 1995 Jul-Aug;328(7-8):604-8. doi: 10.1002/ardp.19953280707. Arch Pharm (Weinheim). 1995. PMID: 7492265

5

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. Among authors: mokrosz mj. Arch Pharm (Weinheim). 1995 Jul-Aug;328(7-8):623-5. doi: 10.1002/ardp.19953280711. Arch Pharm (Weinheim). 1995. PMID: 7492269

6

Structure-activity relationship studies of CNS agents--XVII. Spiro[piperidine-4',1-(1,2,3,4-tetrahydro-beta-carboline)] as a probe defining the extended topographic model of 5-HT1A receptors.

Mokrosz MJ, Duszynska B, Bojarski AJ, Mokrosz JL. Mokrosz MJ, et al. Among authors: mokrosz jl. Bioorg Med Chem. 1995 May;3(5):533-8. doi: 10.1016/0968-0896(95)00039-j. Bioorg Med Chem. 1995. PMID: 7648202

7

Structure-activity relationship studies of CNS agents, XIX: Quantitative analysis of the alkyl chain effects on the 5-HT1A and 5-HT2 receptor affinities of 4-alkyl-1-arylpiperazines and their analogs.

Mokrosz JL, Mokrosz MJ, Charakchieva-Minol S, Paluchowska MH, Bojarski AJ, Duszyńska B. Mokrosz JL, et al. Among authors: mokrosz mj. Arch Pharm (Weinheim). 1995 Feb;328(2):143-8. doi: 10.1002/ardp.19953280210. Arch Pharm (Weinheim). 1995. PMID: 7726740

8

Structure-activity relationship studies of CNS agents. Part 16: A lower limit of a distance between crucial pharmacophores of 5-HT1A ligands.

Mokrosz JL, Mokrosz MJ, Bojarski AJ, Charakchieva-Minol S. Mokrosz JL, et al. Among authors: mokrosz mj. Pharmazie. 1994 Oct;49(10):781-2. Pharmazie. 1994. PMID: 7816905 No abstract available.

9

Structure-activity relationship studies of CNS agents. Part 14: Structural requirements for the 5-HT1A and 5-HT2A receptor selectivity of simple 1-(2-pyrimidinyl)piperazine derivatives.

Mokrosz JL, Strekowski L, Duszyńska B, Harden DB, Mokrosz MJ, Bojarski AJ. Mokrosz JL, et al. Among authors: mokrosz mj. Pharmazie. 1994 Nov;49(11):801-6. Pharmazie. 1994. PMID: 7838864

10

Structure-activity relationship studies of central nervous system agents. 13. 4-[3-(Benzotriazol-1-yl)propyl]-1-(2-methoxyphenyl)piperazine, a new putative 5-HT1A receptor antagonist, and its analogs.

Mokrosz JL, Paluchowska MH, Chojnacka-Wójcik E, Filip M, Charakchieva-Minol S, Dereń-Wesołek A, Mokrosz MJ. Mokrosz JL, et al. Among authors: mokrosz mj. J Med Chem. 1994 Aug 19;37(17):2754-60. doi: 10.1021/jm00043a014. J Med Chem. 1994. PMID: 8064802

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

37 results

Search Page

Filters