Evidence map›Paper›PMID 27424662›Full record

ArticleJournal of enzyme inhibition and medicinal chemistry2016

Comparison of the ligand binding site of CYP2C8 with CYP26A1 and CYP26B1: a structural basis for the identification of new inhibitors of the retinoic acid hydroxylases.

Robert S Foti, Philippe Diaz, Dominique Douguet

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Journal of enzyme inhibition and medicinal chemistry, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.7field-weighted citation impact, top 26% 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

8 citing papers in PubMed, 12 citations in OpenAlex.

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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

3 authors at 3 institutions in 2 countries.

Robert S Fotia Amgen Pharmacokinetics and Drug Metabolism , Cambridge , MA , USA.
Philippe Diazb Department of Biomedical and Pharmaceutical Sciences , Core Laboratory for Neuromolecular Production, University of Montana , Missoula , MT , USA.
Dominique Douguetd CNRS, Institut de Pharmacologie Moléculaire et Cellulaire, Université Nice Sophia Antipolis , Valbonne , France.
Amgen (United States) · USInstitut de Pharmacologie Moléculaire et Cellulaire · FRUniversity of Montana · US

Funding

Inhibition of retinoic acid metabolism for reversal of cognitive deficits in ADR41AG046987 · NIA · DERMAXON, LLC · PI ASTRUC DIAZ, FANNY · 2013 to 2013
$225k
Selective inhibition of CYP26A1 in the skin for the treatment of ichthyosisR41AR069416 · NIAMS · DERMAXON, LLC · PI ASTRUC DIAZ, FANNY · 2016 to 2016
$216k
NIAMS NIH HHS R41 AR069416NIA NIH HHS R41 AG046987
6 · The paper itself

Abstract

The CYP26s are responsible for metabolizing retinoic acid and play an important role in maintaining homeostatic levels of retinoic acid. Given the ability of CYP2C8 to metabolize retinoic acid, we evaluated the potential for CYP2C8 inhibitors to also inhibit CYP26. In vitro assays were used to evaluate the inhibition potencies of CYP2C8 inhibitors against CYP26A1 and CYP26B1. Using tazarotenic acid as a substrate for CYP26, IC

Indexed as

Binding SitesCytochrome P-450 Enzyme InhibitorsCytochrome P-450 Enzyme SystemDose-Response Relationship, DrugHumansLigandsMolecular StructureRetinoic Acid 4-HydroxylaseStructure-Activity RelationshipTretinoinCytochrome P-450 Enzyme InhibitorsCytochrome P-450 Enzyme SystemLigandsRetinoic Acid 4-HydroxylaseTretinoinCYP26CYP2C8homology modelretinoic acidtazarotenic acid

Identifiers

PMID27424662
PMCPMC6628712
OpenAlexW2495918360

What OpenQuestion holds

Textmetadata
LicenceTDM
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.