Evidence map›Paper›PMID 35694688›Full record

ReviewRSC medicinal chemistry2022

Covalent cannabinoid receptor ligands - structural insight and selectivity challenges.

Ian Liddle, Michelle Glass, Joel D A Tyndall, Andrea J Vernall

Abstract readReview
In one paragraph

Review in RSC medicinal chemistry, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Ian LiddleDepartment of Chemistry, University of Otago Dunedin New Zealand andrea.vernall@otago.ac.nz +64 3 479 5214.ORCID https://orcid.org/0000-0003-1196-2419
Michelle GlassDepartment of Pharmacology and Toxicology, University of Otago Dunedin New Zealand.ORCID https://orcid.org/0000-0002-5997-6898
Joel D A TyndallSchool of Pharmacy, University of Otago Dunedin New Zealand.ORCID https://orcid.org/0000-0003-0783-1635
Andrea J VernallDepartment of Chemistry, University of Otago Dunedin New Zealand andrea.vernall@otago.ac.nz +64 3 479 5214.ORCID https://orcid.org/0000-0001-8056-0726

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

X-ray crystallography and cryogenic electronic microscopy have provided significant advancement in the knowledge of GPCR structure and have allowed the rational design of GPCR ligands. The class A GPCRs cannabinoid receptor type 1 and type 2 are implicated in many pathophysiological processes and thus rational design of drug and tool compounds is of great interest. Recent structural insight into cannabinoid receptors has already led to a greater understanding of ligand binding sites and receptor residues that likely contribute to ligand selectivity. Herein, classes of heterocyclic covalent cannabinoid receptor ligands are reviewed in light of the recent advances in structural knowledge of cannabinoid receptors, with particular discussion regarding covalent ligand selectivity and rationale design.

Identifiers

PMID35694688
PMCPMC9132230

What OpenQuestion holds

Textmetadata
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.