Evidence map›Paper›PMID 31952965›Full record

ArticleBioorganic & medicinal chemistry letters2020

Synthesis and biological evaluation of FICZ analogues as agonists of aryl hydrocarbon receptor.

Hao Wu, Binkai Liu, Ka Yang, Gabrielle N Winston-McPherson, Eric D Leisten, Chad M Vezina, William A Ricke, Richard E Peterson, Weiping Tang

Open access · greenAbstract read
In one paragraph

Article in Bioorganic & medicinal chemistry letters, 2020. 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
0.4field-weighted citation impact, top 40% 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, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. 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 1 institution in 1 country.

Hao WuSchool of Pharmacy, University of Wisconsin-Madison, 777 Highland Avenue, Madison, WI 53705, USA.
Binkai LiuSchool of Pharmacy, University of Wisconsin-Madison, 777 Highland Avenue, Madison, WI 53705, USA.
Ka YangSchool of Pharmacy, University of Wisconsin-Madison, 777 Highland Avenue, Madison, WI 53705, USA.
Gabrielle N Winston-McPhersonSchool of Pharmacy, University of Wisconsin-Madison, 777 Highland Avenue, Madison, WI 53705, USA.
Eric D LeistenSchool of Pharmacy, University of Wisconsin-Madison, 777 Highland Avenue, Madison, WI 53705, USA.
Chad M VezinaDepartment of Comparative Biosciences, University of Wisconsin-Madison, School of Veterinary Medicine, Madison, WI 53706, USA; University of Wisconsin-Madison, O'Brien Urology Research Center, Madison, WI, USA.
William A RickeUniversity of Wisconsin-Madison, O'Brien Urology Research Center, Madison, WI, USA; Department of Urology and Carbone Cancer Center, University of Wisconsin-Madison, School of Medicine and Public Health, Madison, WI 53705, USA.
Richard E PetersonSchool of Pharmacy, University of Wisconsin-Madison, 777 Highland Avenue, Madison, WI 53705, USA.
Weiping TangSchool of Pharmacy, University of Wisconsin-Madison, 777 Highland Avenue, Madison, WI 53705, USA; Department of Chemistry, University of Wisconsin-Madison, 1101 University Avenue, Madison, WI 53706, USA. Electronic address: weiping.tang@wisc.edu.
University of Wisconsin–Madison · US

Funding

Role of Beta-Catenin in Urinary DysfunctionU54DK104310 · NIDDK · UNIVERSITY OF WISCONSIN-MADISON · PI BJORLING, DALE EDMOND · 2014 to 2023
$12.8M
REPRODUCTIVE AND DEVELOPMENTAL TOXICITY OF DIOXINR01ES001332 · NIEHS · UNIVERSITY OF WISCONSIN-MADISON · PI PETERSON, RICHARD EUGENE, VEZINA, CHAD M. · 1985 to 2021
$5.3M
NIDDK NIH HHS U54 DK104310NIEHS NIH HHS R01 ES001332
6 · The paper itself

Abstract

The aryl hydrocarbon receptor (AhR) is a ligand activated transcription factor involved in multiple biological processes including immune cell differentiation, intestinal function and inflammation. Based on the scaffold of naturally occurring AhR ligand 6-formylindolo (3,2-b) carbazole (FICZ, 2), a series of analogues has been designed, synthesized and evaluated by cell-based assays. The structure-activity relationships study has successfully led to the discovery of compound 11e with extremely potent activity.

Indexed as

CarbazolesCytochrome P-450 CYP1A1Dose-Response Relationship, DrugHep G2 CellsHumansIndolesMolecular StructureReceptors, Aryl HydrocarbonStructure-Activity RelationshipUp-RegulationCarbazolesCYP1A1 protein, humanCytochrome P-450 CYP1A1IndolesReceptors, Aryl HydrocarbonAhRBenign prostatic hyperplasiaCarbazoleFICZTranscription factor

Identifiers

PMID31952965
PMCPMC7007633
OpenAlexW3000335944

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.