Evidence map›Paper›PMID 35281260›Full record

ArticleFrontiers in molecular biosciences2022

Targeting CB2 and TRPV1: Computational Approaches for the Identification of Dual Modulators.

Paula Morales, Chanté Muller, Nadine Jagerovic, Patricia H Reggio

Open access · goldAbstract read
In one paragraph

Article in Frontiers in molecular biosciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
2.3field-weighted citation impact, top 14% 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

4 citing papers in PubMed, 14 citations in OpenAlex.

  1. Review
  2. Review
  3. Frontiers in neuroinformatics · 2024
    Article
  4. 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

4 authors at 1 institution in 1 country.

Paula MoralesMedicinal Chemistry Institute, Spanish National Research Council, Madrid, Spain.
Chanté MullerDepartment of Chemistry and Biochemistry, University of North Carolina at Greensboro, Greensboro, NC, United States.
Nadine JagerovicMedicinal Chemistry Institute, Spanish National Research Council, Madrid, Spain.
Patricia H ReggioDepartment of Chemistry and Biochemistry, University of North Carolina at Greensboro, Greensboro, NC, United States.
University of North Carolina at Greensboro · US

Funding

The Ionotropic Cannabinoid Receptor TRPV1F31DA053022 · NIDA · UNIVERSITY OF NORTH CAROLINA GREENSBORO · PI MULLER, CHANTÉ · 2021 to 2022
$44k
NIDA NIH HHS F31 DA053022
6 · The paper itself

Abstract

Both metabotropic (CBRs) and ionotropic cannabinoid receptors (ICRs) have implications in a range of neurological disorders. The metabotropic canonical CBRs CB1 and CB2 are highly implicated in these pathological events. However, selective targeting at CB2 versus CB1 offers optimized pharmacology due to the absence of psychoactive outcomes. The ICR transient receptor potential vanilloid type 1 (TRPV1) has also been reported to play a role in CNS disorders. Thus, activation of both targets, CB2 and TRPV1, offers a promising polypharmacological strategy for the treatment of neurological events including analgesia and neuroprotection. This brief research report aims to identify chemotypes with a potential dual CB2/TRPV1 profile. For this purpose, we have rationalized key structural features for activation and performed virtual screening at both targets using curated chemical libraries.

Indexed as

cannabinoidsCB2dual ligandsionotropic receptorsmultitargetingTRPV1

Identifiers

PMID35281260
PMCPMC8914543
OpenAlexW4214515744

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.