Evidence map›Paper›PMID 31363349›Full record

ArticleJournal of undergraduate chemistry research2018

DESIGN AND SYNTHESIS OF DIBENZYLFURAN BASED ETHER AND ESTER DERIVATIVES AS POTENTIAL P450 INHIBITORS.

Navneet Goyal, Kyla Bongay-Williams, Camilla Do, Timothy Perry, Eleanor Kantrow, Miriam Hill-Odom, Jayalakshmi Sridhar, Maryam Foroozesh

Open access · greenAbstract read
In one paragraph

Article in Journal of undergraduate chemistry research, 2018. 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, top 74% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

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

8 authors at 1 institution in 1 country.

Navneet GoyalDepartment of Chemistry, Xavier University of Louisiana, New Orleans, Louisiana 70125.
Kyla Bongay-WilliamsDepartment of Chemistry, Xavier University of Louisiana, New Orleans, Louisiana 70125.
Camilla DoDepartment of Chemistry, Xavier University of Louisiana, New Orleans, Louisiana 70125.
Timothy PerryDepartment of Chemistry, Xavier University of Louisiana, New Orleans, Louisiana 70125.
Eleanor KantrowDepartment of Chemistry, Xavier University of Louisiana, New Orleans, Louisiana 70125.
Miriam Hill-OdomDepartment of Chemistry, Xavier University of Louisiana, New Orleans, Louisiana 70125.
Jayalakshmi SridharDepartment of Chemistry, Xavier University of Louisiana, New Orleans, Louisiana 70125.
Maryam ForoozeshDepartment of Chemistry, Xavier University of Louisiana, New Orleans, Louisiana 70125.
Xavier University of Louisiana · US

Funding

Xavier's RCMI Cancer Research ProgramG12MD007595 · NIMHD · XAVIER UNIVERSITY OF LOUISIANA · PI D'AMOUR, GENE, WANG, GUANGDI · 2012 to 2018
$15.7M
PROJECT PATHWAYS: STUDENT TRAINING CORETL4GM118968 · NIGMS · XAVIER UNIVERSITY OF LOUISIANA · PI FOROOZESH, MARYAM, GIGUETTE, MARGUERITE · 2015 to 2023
$9.2M
Project Pathways: Research Enrichment CoreRL5GM118966 · NIGMS · XAVIER UNIVERSITY OF LOUISIANA · PI FOROOZESH, MARYAM, GIGUETTE, MARGUERITE · 2015 to 2023
$6.6M
RISE Option II at Xavier University of LouisianaR25GM060926 · NIGMS · XAVIER UNIVERSITY OF LOUISIANA · PI FOROOZESH, MARYAM · 2002 to 2016
$3.0M
NIGMS NIH HHS R25 GM060926NIGMS NIH HHS RL5 GM118966NIGMS NIH HHS TL4 GM118968NIMHD NIH HHS G12 MD007595
6 · The paper itself

Abstract

Cytochrome P450 enzymes are a superfamily of hemoproteins involved in the metabolism and detoxification of endogenous and exogenous compounds. P450s are involved in the bioactivation of certain procarcinogens leading to the production of carcinogenic species. This has resulted in P450s' popularity as targets in cancer research. Developing selective and potent mechanism-based inhibitors for these enzymes is expected to be the key to understanding their mechanisms of action, as well as, developing potential anticancer agents. Our group has shown that certain aryl and aryl-alkyl acetylenes act as inhibitors of these enzymes. In an attempt to increase the number of selective P450 inhibitors available for enzymatic studies, five novel dibenzofuran ethers and esters have been designed and synthesized successfully.

Indexed as

AcetylenesCytochrome P450 EnzymesEnzyme InhibitorsMetabolismOrganic SynthesisPropargyl Pyridinyl EthersSuicide Inhibitors

Identifiers

PMID31363349
PMCPMC6667160
OpenAlexW3025749632

What OpenQuestion holds

Textmetadata
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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.