Evidence map›Paper›PMID 38139366›Full record

ReviewInternational journal of molecular sciences2023

Synephrine and Its Derivative Compound A: Common and Specific Biological Effects.

Svetlana A Dodonova, Ekaterina M Zhidkova, Alexey A Kryukov, Timur T Valiev, Kirill I Kirsanov, Evgeny P Kulikov, Irina V Budunova, Marianna G Yakubovskaya, Ekaterina A Lesovaya

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
3.4field-weighted citation impact, top 8% 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

11 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Synephrine Inhibits Oxidative Stress and HCell biochemistry and biophysics · 2025
    Article
  7. Review
  8. Review
  9. Article
  10. Article
  11. 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

9 authors at 4 institutions in 2 countries.

Svetlana A DodonovaResearch Institute of Experimental Medicine, Department of Pathophysiology, Kursk State Medical University, 305041 Kursk, Russia.ORCID 0000-0001-8491-3082
Ekaterina M ZhidkovaDepartment of Chemical Carcinogenesis, N.N. Blokhin National Medical Research Center of Oncology, 115478 Moscow, Russia.ORCID 0000-0003-3318-9391
Alexey A KryukovResearch Institute of Experimental Medicine, Department of Pathophysiology, Kursk State Medical University, 305041 Kursk, Russia.ORCID 0000-0002-3181-7828
Timur T ValievDepartment of Chemical Carcinogenesis, N.N. Blokhin National Medical Research Center of Oncology, 115478 Moscow, Russia.
Kirill I KirsanovDepartment of Chemical Carcinogenesis, N.N. Blokhin National Medical Research Center of Oncology, 115478 Moscow, Russia.ORCID 0000-0002-8599-6833
Evgeny P KulikovLaboratory of Single Cell Biology, Russian University of People's Friendship (RUDN) University, 117198 Moscow, Russia.
Irina V BudunovaDepartment of Dermatology, Northwestern University, Chicago, IL 60611, USA.ORCID 0000-0001-5880-6822
Marianna G YakubovskayaDepartment of Chemical Carcinogenesis, N.N. Blokhin National Medical Research Center of Oncology, 115478 Moscow, Russia.ORCID 0000-0002-9710-8178
Ekaterina A LesovayaDepartment of Chemical Carcinogenesis, N.N. Blokhin National Medical Research Center of Oncology, 115478 Moscow, Russia.ORCID 0000-0002-1967-9637
Institute of Experimental Medicine · RUPeoples' Friendship University of Russia · RURyazan State Medical University named after Academician I.P. Pavlov · RUNorthwestern University · US

Funding

Russian Science Foundation 23-15-00321
6 · The paper itself

Abstract

This review is focused on synephrine, the principal phytochemical found in bitter orange and other medicinal plants and widely used as a dietary supplement for weight loss/body fat reduction. We examine different aspects of synephrine biology, delving into its established and potential molecular targets, as well as its mechanisms of action. We present an overview of the origin, chemical composition, receptors, and pharmacological properties of synephrine, including its anti-inflammatory and anti-cancer activity in various in vitro and animal models. Additionally, we conduct a comparative analysis of the molecular targets and effects of synephrine with those of its metabolite, selective glucocorticoid receptor agonist (SEGRA) Compound A (CpdA), which shares a similar chemical structure with synephrine. SEGRAs, including CpdA, have been extensively studied as glucocorticoid receptor activators that have a better benefit/risk profile than glucocorticoids due to their reduced adverse effects. We discuss the potential of synephrine usage as a template for the synthesis of new generation of non-steroidal SEGRAs. The review also provides insights into the safe pharmacological profile of synephrine.

Indexed as

CitrusSynephrineAnimalsAnti-Inflammatory AgentsPlant ExtractsReceptors, GlucocorticoidAnti-Inflammatory AgentsPlant ExtractsReceptors, GlucocorticoidSynephrinebeta-adrenergic receptorscancercardiovascular systemCpdAglucocorticoidsinflammationmetabolic disordersselective glucocorticoid receptor activatorsynephrine

Identifiers

PMID38139366
PMCPMC10744207
OpenAlexW4389895146

What Socratic 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 Socratic graph.