Paluchowska MH - Search Results

1

New 1,2,4-oxadiazole derivatives with positive mGlu₄ receptor modulation activity and antipsychotic-like properties.

Stankiewicz A, Kaczorowska K, Bugno R, Kozioł A, Paluchowska MH, Burnat G, Chruścicka B, Chorobik P, Brański P, Wierońska JM, Duszyńska B, Pilc A, Bojarski AJ. Stankiewicz A, et al. Among authors: paluchowska mh. J Enzyme Inhib Med Chem. 2022 Dec;37(1):211-225. doi: 10.1080/14756366.2021.1998022. J Enzyme Inhib Med Chem. 2022. PMID: 34894953 Free PMC article.

2

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: paluchowska mh. Arch Pharm (Weinheim). 1995 Jul-Aug;328(7-8):604-8. doi: 10.1002/ardp.19953280707. Arch Pharm (Weinheim). 1995. PMID: 7492265

3

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

4

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: paluchowska mh. Arch Pharm (Weinheim). 1995 Feb;328(2):143-8. doi: 10.1002/ardp.19953280210. Arch Pharm (Weinheim). 1995. PMID: 7726740

5

Structure-activity relationship studies of CNS agents, XV: N-[omega-(4-aryl-1-piperazinyl)alkyl]-2-oxo-1,2,3,4-tetrahydroquinoline s and -4-oxo-1,2,3,4-tetrahydropyrazino[1,2-a]indoles: new, highly potent 5-HT1A ligands.

Mokrosz JL, Duszyńska B, Paluchowska MH. Mokrosz JL, et al. Among authors: paluchowska mh. Arch Pharm (Weinheim). 1994 Aug;327(8):529-31. doi: 10.1002/ardp.19943270811. Arch Pharm (Weinheim). 1994. PMID: 7944908 No abstract available.

6

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: paluchowska mh. J Med Chem. 1994 Aug 19;37(17):2754-60. doi: 10.1021/jm00043a014. J Med Chem. 1994. PMID: 8064802

7

On the bioactive conformation of NAN-190 (1) and MP3022 (2), 5-HT(1A) receptor antagonists.

Paluchowska MH, Mokrosz MJ, Bojarski A, Wesołowska A, Borycz J, Charakchieva-Minol S, Chojnacka-Wójcik E. Paluchowska MH, et al. J Med Chem. 1999 Dec 2;42(24):4952-60. doi: 10.1021/jm991045h. J Med Chem. 1999. PMID: 10585205

8

Influence of the aliphatic spacer length on the 5-HT1A receptor activity of new arylpiperazines with an indazole system.

Paluchowska MH, Duszyńska B, Kłodzińska A, Tatarczyńska E. Paluchowska MH, et al. Pol J Pharmacol. 2000 May-Jun;52(3):209-16. Pol J Pharmacol. 2000. PMID: 11055578

9

Active conformation of some arylpiperazine postsynaptic 5-HT(1A) receptor antagonists.

Paluchowska MH, Bojarski AJ, Charakchieva-Minol S, Wesołowska A. Paluchowska MH, et al. Eur J Med Chem. 2002 Apr;37(4):273-83. doi: 10.1016/s0223-5234(01)01312-5. Eur J Med Chem. 2002. PMID: 11960662

10

Substitution mode of the amide fragment in some new N-[omega-[4-(2-methoxyphenyl)piperazin-1-yl]alkyl]pyrid-2(1H)-ones and their 5-HT1A/5-HT2A activity.

Paluchowska MH, Bugno R, Charakchieva-Minol S, Bojarski AJ, Wesołowska A. Paluchowska MH, et al. Pol J Pharmacol. 2001 Jul-Aug;53(4):369-76. Pol J Pharmacol. 2001. PMID: 11990083 Free article.

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