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dr Andrzej J. Bojarski

e-mail:
phone: +48-12-6623365
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interest(s):

Affiliation:


Polish Academy of Sciences. Institute of Pharmacology

address: Smętna 12, Kraków, 31-343, Poland
phone: +48-12-6623220
fax: +48-012-6374500
web: http://www.if-pan.krakow.pl

Participant:


V Multidyscyplinarna Konferencja Nauki o Leku

began: 2006-05-15
ended: 2006-05-17
Presented:

V Multidyscyplinarna Konferencja Nauki o Leku

NEW DUAL 5-HT7/5-HT1A LIGANDS WITH ANTIDEPRESSANT AND ANXIOLYTIC-LIKE ACTIVITY

Participant:


VI Multidyscyplinarna Konferencja Nauki o Leku

began: 2008-05-25
ended: 2008-05-29
Presented:

VI Multidyscyplinarna Konferencja Nauki o Leku

Searching for lead molecules as potential new CNS agents in the serotonin 5-HT6 screening assay

Participant:


VII Multidyscyplinarna Konferencja Nauki o Leku

began: 2010-05-09
ended: 2010-05-13
Presented:

Publications:


  1. 2-(1-Arylsulfonylpiperidin-2-yl)ethyl derivatives as 5-HT7 receptor ligands: synthesis and their affinity for 5-HT1A/5-HT2A/5-HT7/D2 receptors
  2. 8-ALKOXY-PURINE-2,6-DIONES WITH 7-PHENYLPIPERAZINYLALKYL AND 7-TETRAHYDRO-ISOQUINOLINYLALKYL MOIETIES AS 5-HT1A, 5-HT2A, 5-HT7 RECEPTOR LIGANDS
  3. Alkyl-nitroquipazine derivatives as serotonin transporter and 5-HT1A receptor ligands
  4. CHO cell line with stable expression of the HTRA1 gene as a tool for studying functional activity of 5-HT1A receptor ligands
  5. Crystal structure of β-adrenergic receptor as a new template in homology modeling of GPCR. Application to serotonin 5-HT1A and 5-HT7 receptors
  6. DESIGN AND SYNTHESIS OF NEW 7-PHENYLPIPERAZINYLALKYL AND 7-TETRAHYDROISOQUINOLINYLALKYL DERIVATIVES OF PURINE-2,6,8-TRIONE AS POTENTIAL SEROTONIN RECEPTOR AGENTS
  7. Examination of 5-HT6 receptor affinity in the group of arylsulfonamide derivatives
  8. Homology modeling of G-protein coupled receptors
  9. Identification of Novel 5-HT7R Ligands via Multistep Virtual Screening of Commercially Available Compounds Databases
  10. Interaction fingerprints patterns. Binding mode analysis of mGlu2 receptor model based on docking studies
  11. Ligand-directed receptor trafficking
  12. Mannich bases, 5-arylimidazolidine-2,4-dione derivatives with arylpiperazine moiety, as 5-HT1A receptor ligands with serotonin transporter affinity
  13. Molecular modeling explains differences in binding affinity of new potent and selective 5-HT1A ligands: arylpiperazinylalkylthiobenzoxazole derivatives
  14. NEW DUAL 5-HT7/5-HT1A LIGANDS WITH ANTIDEPRESSANT AND ANXIOLYTIC-LIKE ACTIVITY
  15. New serotonin receptors ligands in the group of 8-acylamide derivatives of 1,3-dimethyl-7-[(4-phenyl- piperazin-1-yl)-alkyl]-1H-purine-2,6-(3H,7H)-dione
  16. Quinolinesulfonamides as potential 5-HT7 and 5-HT1A receptor ligands
  17. Rational design and synthesis of new 5-HT6R ligands with the use of bioisosteric strategies. Crystal structures, biological evaluation and molecular modeling studies.
  18. SAR studies of novel 5-HT7R ligands with different spacers between aryl and amine moieties
  19. Searching for lead molecules as potential new CNS agents in the serotonin 5-HT6 screening assay
  20. Serotonin transporter inhibitors inducing hypothermia at mice
  21. Solid-phase synthesis and preliminary biological investigation of arylpiperazine library as 5-HT1A and 5-HT2A receptor ligands
  22. Synthesis and serotonin receptors activity of new purine-2,6-dione derivatives with arylpiperazinylalkoxy moieties
  23. Synthesis, anticonvulsant activity and 5-HT1A/5-HT7 receptors affinity of new 1-[(4-substituted-  piperazin-1-yl)-alkyl]- 3-methyl- 3-(2-methylpropyl)-pyrrolidine- 2,5-diones
  24. Synthesis of long-chain arylpiperazine theophylline derivatives as potential 5-HT7 and 5-HT6 receptors ligands
  25. Synthesis of novel pyrido[1,2-c]pyrimidine derivatives as selective ligands for 5-HT1A receptors
  26. THE BIOLOGICAL TARGET DERIVED PHARMACOPHORIC MODEL FOR 5-HT7 SEROTONIN RECEPTOR ANTAGONISM
  27. The ligand binding to the serotonin transporter
  28. The multiobjective based design, synthesis and evaluation of the arylsulfonamide/amide derivatives of arylxyethyl- and arylthioethyl- piperidines and pyrrolidines as a novel class of potent 5-HT7 receptor antagonists



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