Evidence map›Paper›PMID 37985681›Full record

ArticleScientific reports2023

Synthesis and biochemical evaluation of 17-N-beta-aminoalkyl-4,5α-epoxynormorphinans.

Ferenc Ötvös, Edina Szűcs, Ákos Urai, István Köteles, Pál T Szabó, Zsuzsanna Katalin Varga, Dávid Gombos, Sándor Hosztafi, Sándor Benyhe

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.7field-weighted citation impact, top 28% of its field
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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. Directions for analgesic development.Journal of anesthesia and translational medicine · 2024
    Review
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

9 authors at 4 institutions in 2 countries.

Ferenc Ötvös *Institute of Biochemistry, HUN-REN Biological Research Centre, Temesvári Krt. 62, 6726, Szeged, Hungary. otvos@brc.hu.ORCID 0000-0001-7630-5466
Edina Szűcs *Institute of Biochemistry, HUN-REN Biological Research Centre, Temesvári Krt. 62, 6726, Szeged, Hungary.
Ákos Urai *Institute of Pharmaceutical Chemistry, Semmelweis Medical University, Hőgyes Endre Utca 9, 1092, Budapest, Hungary.
István KötelesInstitute of Pharmaceutical Chemistry, Semmelweis Medical University, Hőgyes Endre Utca 9, 1092, Budapest, Hungary.
Pál T SzabóResearch Centre for Natural Sciences, MS Metabolomics Research Laboratory, Magyar Tudósok Krt. 2, 1117, Budapest, Hungary.
Zsuzsanna Katalin VargaInstitute of Biochemistry, HUN-REN Biological Research Centre, Temesvári Krt. 62, 6726, Szeged, Hungary.
Dávid GombosInstitute of Biochemistry, HUN-REN Biological Research Centre, Temesvári Krt. 62, 6726, Szeged, Hungary.
Sándor HosztafiInstitute of Pharmaceutical Chemistry, Semmelweis Medical University, Hőgyes Endre Utca 9, 1092, Budapest, Hungary.
Sándor BenyheInstitute of Biochemistry, HUN-REN Biological Research Centre, Temesvári Krt. 62, 6726, Szeged, Hungary. benyhe@brc.hu.
HUN-REN Szegedi Biológiai Kutatóközpont · HUSemmelweis University · HUUniversity of Szeged · HUHUN-REN Research Centre for Natural Sciences · HU

Funding

Országos Tudományos Kutatási Alapprogramok (Hungarian Scientific Research Fund) OTKA-108518
6 · The paper itself

Abstract

Opiate alkaloids and their synthetic derivatives are still widely used in pain management, drug addiction, and abuse. To avoid serious side effects, compounds with properly designed pharmacological profiles at the opioid receptor subtypes are long needed. Here a series of 17-N-substituted derivatives of normorphine and noroxymorphone analogues with five- and six-membered ring substituents have been synthesized for structure-activity study. Some compounds showed nanomolar affinity to MOR, DOR and KOR in in vitro competition binding experiments with selective agonists [

Indexed as

Receptors, OpioidReceptors, Opioid, muBinding, CompetitiveMolecular Docking SimulationReceptors, Opioid, kappaStructure-Activity RelationshipReceptors, OpioidReceptors, Opioid, kappaReceptors, Opioid, mu

Identifiers

PMID37985681
PMCPMC10660610
OpenAlexW4388818685

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.