Evidence map›Paper›PMID 36770761›Full record

ArticleMolecules (Basel, Switzerland)2023

Impact of the Substitution Pattern at the Basic Center and Geometry of the Amine Fragment on 5-HT

Katarzyna Grychowska, Wojciech Pietruś, Ludmiła Kulawik, Ophélie Bento, Grzegorz Satała, Xavier Bantreil, Frédéric Lamaty, Andrzej J Bojarski, Joanna Gołębiowska, Agnieszka Nikiforuk and 4 more

Abstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
  2. Intepirdine Derivatives Possessing Dual 5HT6 Antagonism / HDAC6 Inhibitory Activity.Chemistry (Weinheim an der Bergstrasse, Germany) · 2025
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Katarzyna GrychowskaFaculty of Pharmacy, Jagiellonian University Medical College, 9 Medyczna Str., 30-688 Kraków, Poland.
Wojciech PietruśMaj Institute of Pharmacology, Polish Academy of Sciences, 12 Smętna Str., 31-324 Kraków, Poland.ORCID 0000-0002-8563-7929
Ludmiła KulawikFaculty of Pharmacy, Jagiellonian University Medical College, 9 Medyczna Str., 30-688 Kraków, Poland.
Ophélie BentoInstitut de Génomique Fonctionelle, Université de Montpellier, CNRS INSERM, 34094 Montpellier, France.
Grzegorz SatałaMaj Institute of Pharmacology, Polish Academy of Sciences, 12 Smętna Str., 31-324 Kraków, Poland.
Xavier BantreilIBMM, Université de Montpellier, CNRS, ENSCM, 34094 Montpellier, France.ORCID 0000-0002-2676-6851
Frédéric LamatyIBMM, Université de Montpellier, CNRS, ENSCM, 34094 Montpellier, France.
Andrzej J BojarskiMaj Institute of Pharmacology, Polish Academy of Sciences, 12 Smętna Str., 31-324 Kraków, Poland.ORCID 0000-0003-1417-6333
Joanna GołębiowskaMaj Institute of Pharmacology, Polish Academy of Sciences, 12 Smętna Str., 31-324 Kraków, Poland.ORCID 0000-0003-2250-2995
Agnieszka NikiforukMaj Institute of Pharmacology, Polish Academy of Sciences, 12 Smętna Str., 31-324 Kraków, Poland.ORCID 0000-0002-2424-8348
Philippe MarinInstitut de Génomique Fonctionelle, Université de Montpellier, CNRS INSERM, 34094 Montpellier, France.ORCID 0000-0002-5977-7274
Séverine Chaumont-DubelInstitut de Génomique Fonctionelle, Université de Montpellier, CNRS INSERM, 34094 Montpellier, France.ORCID 0000-0001-6860-6891
Rafał KurczabMaj Institute of Pharmacology, Polish Academy of Sciences, 12 Smętna Str., 31-324 Kraków, Poland.ORCID 0000-0002-9555-3905
Paweł ZajdelFaculty of Pharmacy, Jagiellonian University Medical College, 9 Medyczna Str., 30-688 Kraków, Poland.ORCID 0000-0002-6192-8721

Funding

National Science Center DEC-2019/03/X/NZ7/01894Priority Research Area qLife "Excellence Initiative Research University" at the Jagiellonian University in Krakow
6 · The paper itself

Abstract

Salt bridge (SB, double-charge-assisted hydrogen bonds) formation is one of the strongest molecular non-covalent interactions in biological systems, including ligand-receptor complexes. In the case of G-protein-coupled receptors, such an interaction is formed by the conserved aspartic acid (D3.32) residue and the basic moiety of the aminergic ligand. This study aims to determine the influence of the substitution pattern at the basic nitrogen atom and the geometry of the amine moiety at position 4 of 1

Indexed as

QuinolinesSerotoninAminesLigandsReceptors, Dopamine D3Receptors, SerotoninSerotonin AntagonistsStructure-Activity RelationshipAminesLigandsQuinolinesReceptors, Dopamine D3Receptors, SerotoninSerotoninSerotonin Antagonists5-HT6R antagonistsD3R ligandsdual-acting compoundsmolecular dynamicssalt bridge formation

Identifiers

PMID36770761
PMCPMC9920808

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.