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OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

Pyrroloquinoline scaffold-based 5-HT6R ligands: Synthesis, quantum chemical and molecular dynamic studies, and influence of nitrogen atom position in the scaffold on affinity
Katarzyna Grychowska, Rafał Kurczab, Paweł Śliwa, et al.
Bioorganic & Medicinal Chemistry (2018) Vol. 26, Iss. 12, pp. 3588-3595
Closed Access | Times Cited: 16

Showing 16 citing articles:

Biological properties of pyrroloquinoline and pyrroloisoquinoline derivatives
Petra Králová, Miroslav Soural
European Journal of Medicinal Chemistry (2024) Vol. 269, pp. 116287-116287
Closed Access | Times Cited: 4
Dual 5-HT6 and D3 Receptor Antagonists in a Group of 1H-Pyrrolo[3,2-c]quinolines with Neuroprotective and Procognitive Activity
Katarzyna Grychowska, Séverine Chaumont‐Dubel, Rafał Kurczab, et al.
ACS Chemical Neuroscience (2019) Vol. 10, Iss. 7, pp. 3183-3196
Open Access | Times Cited: 29
A dual-acting 5-HT6 receptor inverse agonist/MAO-B inhibitor displays glioprotective and pro-cognitive properties
Vittorio Canale, Katarzyna Grychowska, Rafał Kurczab, et al.
European Journal of Medicinal Chemistry (2020) Vol. 208, pp. 112765-112765
Open Access | Times Cited: 22
Imidazopyridine-Based 5-HT6 Receptor Neutral Antagonists: Impact of N1-Benzyl and N1-Phenylsulfonyl Fragments on Different Receptor Conformational States
David Vanda, Vittorio Canale, Séverine Chaumont‐Dubel, et al.
Journal of Medicinal Chemistry (2021) Vol. 64, Iss. 2, pp. 1180-1196
Closed Access | Times Cited: 20
Computer-Aided Studies for Novel Arylhydantoin 1,3,5-Triazine Derivatives as 5-HT6 Serotonin Receptor Ligands with Antidepressive-Like, Anxiolytic and Antiobesity Action In Vivo
Rafał Kurczab, Wesam Ali, Dorota Łażewska, et al.
Molecules (2018) Vol. 23, Iss. 10, pp. 2529-2529
Open Access | Times Cited: 23
Chlorine substituents and linker topology as factors of 5-HT6R activity for novel highly active 1,3,5-triazine derivatives with procognitive properties in vivo
Sylwia Sudoł, Katarzyna Kucwaj‐Brysz, Rafał Kurczab, et al.
European Journal of Medicinal Chemistry (2020) Vol. 203, pp. 112529-112529
Open Access | Times Cited: 19
Introduction of Carbon Substituents into Nitroarenes via Nucleophilic Substitution of Hydrogen: New Developments
Rafał Loska, Mieczysław Mąkosza
Synthesis (2020) Vol. 52, Iss. 21, pp. 3095-3110
Closed Access | Times Cited: 16
An Approach to Pharmacological Targets of Pyrrole Family From Medicinal Chemistry Viewpoint
Mohsen Amini, Ebrahim Saeedian Moghadam, Katayoon Mireskandari, et al.
Mini-Reviews in Medicinal Chemistry (2022) Vol. 22, Iss. 19, pp. 2486-2561
Closed Access | Times Cited: 9
Design, synthesis and molecular modelling of new bulky Fananserin derivatives with altered pharmacological profile as potential antidepressants
Przemysław Zaręba, Jolanta Jaśkowska, Izabela Czekaj, et al.
Bioorganic & Medicinal Chemistry (2019) Vol. 27, Iss. 15, pp. 3396-3407
Closed Access | Times Cited: 15
Water-acetic acid mediated an efficient one-pot eco-friendly synthesis of novel bis-isoxazolopyrroloquinoline derivatives
Sri Venkateswarlu Rayudu, Dipankar Karmakar, Pramod Kumar
Tetrahedron Letters (2019) Vol. 60, Iss. 36, pp. 151025-151025
Closed Access | Times Cited: 15
Chemical puzzles in the search for new, flexible derivatives of lurasidone as antipsychotic drugs
Przemysław Zaręba, Anna K. Drabczyk, Jolanta Jaśkowska, et al.
Bioorganic & Medicinal Chemistry (2020) Vol. 28, Iss. 10, pp. 115459-115459
Open Access | Times Cited: 13
2-Phenyl-1H-pyrrole-3-carboxamide as a New Scaffold for Developing 5-HT6 Receptor Inverse Agonists with Cognition-Enhancing Activity
Marcin Drop, Vittorio Canale, Séverine Chaumont‐Dubel, et al.
ACS Chemical Neuroscience (2021) Vol. 12, Iss. 7, pp. 1228-1240
Open Access | Times Cited: 12
Rh(III)-Catalyzed C(7)–H Alkylation of Quinolines in the Synthesis of Angular π-Extended Pyrroloquinolines for Single-Component White-Light Emission
Nandkishor Prakash Khot, Paritosh Mahato, T. K. Sajeev, et al.
Organic Letters (2022) Vol. 24, Iss. 11, pp. 2186-2191
Closed Access | Times Cited: 7
Impact of the Substitution Pattern at the Basic Center and Geometry of the Amine Fragment on 5-HT6 and D3R Affinity in the 1H-Pyrrolo[3,2-c]quinoline Series
Katarzyna Grychowska, Wojciech Pietruś, Ludmiła Kulawik, et al.
Molecules (2023) Vol. 28, Iss. 3, pp. 1096-1096
Open Access | Times Cited: 1
The use of machine learning-based sequential virtual screening in the search of new ligands of 5-HT6 receptor
Michał Sapa, Alicja Gawalska, Marcin Kołaczkowski, et al.
Farmacja Polska (2023) Vol. 78, Iss. 11, pp. 607-614
Open Access
Tricyclic Systems: Central Carbocyclic Ring With Fused Five- and Six-Membered Rings
Stephen P. Wren
Elsevier eBooks (2020), pp. 1003-1019
Closed Access
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