Department of Medicinal Chemistry
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Department of Medicinal Chemistry

Scientific profile
- Employees
Pracownicy zakładu
Ryszard Bugno, dr
Rafał Kurczab, dr hab.
Sabina Podlewska, dr hab.
Grzegorz Satała, dr
Katarzyna Szczepańska, dr
Adam Hogendorf, dr
Katarzyna Kaczorowska, dr
Janusz Malarz, dr
Wojciech Pietruś, dr
Dawid Warszycki, dr
Aneta Kozioł
Krystyna Nędza
Achievements
- Publications
- Grants
Grant
Development of protocol for in silico design of compounds inhibit Ebola virus infection
Dawid Warszycki, PhD
8-[4-[2-(1,2,3,4-tetrahydroisoquinolinyl)]butyl]-8-azaspiro[4,5]decane-7,9-dione: A new 5-HT1A receptor ligand with the same activity profile as buspirone
Mokrosz, JL, DerenWesolek, A, Tatarczynska, E, Duszynska, B, Bojarski, AJ, Mokrosz, MJ, ChojnackaWojcik, E
DOI: 10.1021/JM950662C
8-[4-[2-(1,2,3,4-tetrahydroisoquinolinyl)]butyl]-8-azaspiro[4.5]decane-7,9- dione: A new 5-HT<inf>1A</inf> receptor ligand with the same activity profile as buspirone
Mokrosz, J.L., Dereń-Wesołek, A., Tatarczyńska, E., Duszyńska, B., Bojarski, A.J., Mokrosz, M.J., Chojnacka-Wójcik, E.
DOI:
Structure-activity relationship studies of CNS agents. Part 29. N-Methylpiperazino-substituted derivatives of quinazoline, phthalazine and quinoline as novel α<inf>1</inf>, 5-HT(1A) and 5-HT(2A) receptor ligands
Mokrosz, J.L., Duszyńska, B., Charakchieva-Minol, S., Bojarski, A.J., Mokrosz, M.J., Wydra, R.L., Janda, L., Strekowski, L.
DOI: 10.1016/S0223-5234(97)86176-4
Conformational analysis of 4-(2'-furyl)-2-(methylamino)pyrimidine
Mokrosz, J.L., Bojarski, A.J., Harden, D.B., Strekowski, L.
DOI: 10.1002/jhet.5570330434
RESTRICTED ROTATION IN 3-(1-NAPHTHYL)-2-THIOHYDANTOIN
RYCZEK, J, BOJARSKI, AJ, SZNELER, E, MOKROSZ, JL
DOI:
IONIZATION-CONSTANTS OF THE MODEL N-ALKYL SUBSTITUTED CYCLIC AMINES
BOJARSKI, AJ, MOKROSZ, MJ, PALUCHOWSKA, MH
DOI:
Ionization constants of the model N-alkyl substituted cyclic amines
Bojarski, A.J., Mokrosz, M.J., Paluchowska, M.H.
DOI:
Structure‐Activity Relationship Studies of CNS Agents, XXI: Two Derivatives of 1‐(o‐Methoxyphenyl)piperazine with an Opposite Function at 5‐HT<inf>1A</inf> Receptors,Struktur‐Wirkung‐Beziehungen ZNS‐aktiver Substanzen, 21. Mitt.<sup>1)</sup>: Zwei Derivate von 1‐(o‐Methoxyphenyl)piperazin mit entgegengesetzter Wirkung auf 5‐HT<inf>1A</inf> Rezeptoren
Mokrosz, J.L., Klodzinska, A., Boksa, J., Bojarski, A.J., Duszynska, B., Chojnacka‐Wójcik, E.
DOI: 10.1002/ardp.19953280417
Structure‐Activity Relationship Studies of CNS Agents, Part 23<sup>[1])</sup>: N‐(3‐Phenylpropyl)‐ and N‐[3(E)‐Cinnamyl]‐1,2,3,4‐tetrahydroisoquinoline Mimic 1‐Phenylpiperazine at 5‐HT<inf>1A</inf> Receptors
Mokrosz, J.L., Bojarski, A.J., Charakchieva‐Minol, S., Duszynska, B., Mokrosz, M.J., Paluchowska, M.H.
DOI: 10.1002/ardp.19953280707
Structure-activity relationship studies of CNS agents-XVII. Spiro[piperidine-4′,1-(1,2,3,4-tetrahydro-β-carboline)] as a probe defining the extended topographic model of 5-HT<inf>1A</inf>receptors
Mokrosz, M.J., Duszynska, B., Bojarski, A.J., Mokrosz, J.L.
DOI: 10.1016/0968-0896(95)00039-J