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International Journal of Molecular Sciences|January 26, 2021
Low Basicity as a Characteristic for Atypical Ligands of Serotonin Receptor 5-HT2Sabina Podlewska, Ryszard Bugno, Enza Lacivita, et al.Polish Journal of Pharmacology|July 18, 2003
Novel N-[omega-[4-(2-methoxyphenyl)piperazin-1-yl]-ethyl]pyrid-2(1H)-ones with diversified 5-HT1A receptor activityMaria H Paluchowska, Ryszard Bugno, Sijka Charakchieva-Minol, et al.Journal of Chemical Information and Modeling|May 11, 2026
Decoding Prolonged Residence Time of 5-HT2A Receptor Antagonists: Insights from Ritanserin DerivativesSzymon K Kordylewski, Kinga Kurowska, Krystyna Nędza, et al.Journal of Psychopharmacology (Oxford, England)|August 28, 2019
Serotonin type 5A receptor antagonists inhibit D-lysergic acid diethylamide discriminatory cue in ratsPiotr Popik, Martyna Krawczyk, Agata Kuziak, et al.Bioorganic & Medicinal Chemistry|February 9, 2010
SAR studies on new bis-aryls 5-HT7 ligands: Synthesis and molecular modelingEduard Badarau, Ryszard Bugno, Franck Suzenet, et al.The Journal of Pharmacy and Pharmacology|February 18, 2017
Inhibition of PDE5A1 guanosine cyclic monophosphate (cGMP) hydrolysing activity by sildenafil analogues that inhibit cellular cGMP effluxAnna Subbotina, Aina W Ravna, Roy A Lysaa, et al.Pharmaceutics|January 21, 2022
Comparison of an Addictive Potential of μ-Opioid Receptor Agonists with G Protein Bias: Behavioral and Molecular Modeling StudiesLucja Kudla, Ryszard Bugno, Sabina Podlewska, et al.Archiv Der Pharmazie|August 31, 2006
Conformational restriction in novel NAN-190 and MP3022 analogs and their 5-HT(1A) receptor activityMaria H Paluchowska, Ryszard Bugno, Sijka Charakchieva-Minol, et al.Bioorganic & Medicinal Chemistry|September 11, 2007
The influence of modifications in imide fragment structure on 5-HT(1A) and 5-HT(7) receptor affinity and in vivo pharmacological properties of some new 1-(m-trifluoromethylphenyl)piperazinesMaria H Paluchowska, Ryszard Bugno, Beata Duszyńska, et al.Bioorganic & Medicinal Chemistry|November 4, 2005
Structure-intrinsic activity relationship studies in the group of 1-imido/amido substituted 4-(4-arylpiperazin-1-yl)cyclohexane derivatives; new, potent 5-HT1A receptor agents with anxiolytic- like activityAndrzej J Bojarski, Maria H Paluchowska, Beata Duszyńska, et al.Pageof 4