Evidence map›Paper›PMID 29426628›Full record

ArticleBioorganic & medicinal chemistry2018

Design, synthesis, and biological evaluation of inhibitors of the NADPH oxidase, Nox4.

Qian Xu, Amol A Kulkarni, Ayyiliath M Sajith, Dilbi Hussein, David Brown, Osman F Güner, M Damoder Reddy, E Blake Watkins, Bernard Lassègue, Kathy K Griendling and 1 more

Abstract read
In one paragraph

Article in Bioorganic & medicinal chemistry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Review
  2. Article
  3. Design, synthesis, and screening of sulfonylurea-derived NLRP3 inflammasome inhibitors.Medicinal chemistry research : an international journal for rapid communications on design and mechanisms of action of biologically active agents · 2020
    Article
  4. Article
  5. Article
  6. 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

11 authors.

Qian XuDivision of Cardiology, Department of Medicine, Emory University, Atlanta, GA 30322, USA.
Amol A KulkarniDepartment of Pharmaceutical Sciences, College of Pharmacy, Howard University, Washington, DC 20059, USA. Electronic address: amol.kulkarni@Howard.edu.
Ayyiliath M SajithDepartment of Pharmaceutical Sciences, College of Pharmacy, Howard University, Washington, DC 20059, USA.
Dilbi HusseinDepartment of Pharmaceutical Sciences, College of Pharmacy, Howard University, Washington, DC 20059, USA.
David BrownDivision of Cardiology, Department of Medicine, Emory University, Atlanta, GA 30322, USA.
Osman F GünerDepartment of Pharmaceutical Sciences, College of Pharmacy, Mercer University, Atlanta, GA 30341, USA; Current address: Department of Chemistry and Physics, Santa Rosa Junior College, Santa Rosa, CA 95401, USA.
M Damoder ReddyDepartment of Pharmaceutical Sciences, College of Pharmacy, Union University, Jackson, TN 38305, USA.
E Blake WatkinsDepartment of Pharmaceutical Sciences, College of Pharmacy, Union University, Jackson, TN 38305, USA.
Bernard LassègueDivision of Cardiology, Department of Medicine, Emory University, Atlanta, GA 30322, USA.
Kathy K GriendlingDivision of Cardiology, Department of Medicine, Emory University, Atlanta, GA 30322, USA.
J Phillip BowenDepartment of Pharmaceutical Sciences, College of Pharmacy, Mercer University, Atlanta, GA 30341, USA. Electronic address: bowen_jp@mercer.edu.

Funding

T cell triggering events and hypertensionP01HL095070 · NHLBI · EMORY UNIVERSITY · PI JO, HANJOONG · 2009 to 2019
$20.5M
Purchase of a Thermo Fisher Scientific LTQ Orbitrap XL Mass SpectrometerS10RR028859 · NCRR · UNIVERSITY OF GEORGIA · PI AMSTER, I JONATHAN · 2011 to 2011
$832k
NCRR NIH HHS S10 RR028859NHLBI NIH HHS P01 HL095070
6 · The paper itself

Abstract

NADPH oxidases (Nox enzymes) are critical mediators of both physiologic and pathophysiologic processes. Nox enzymes catalyze NADPH-dependent generation of reactive oxygen species (ROS), including superoxide and hydrogen peroxide. Until recently, Nox4 was proposed to be involved exclusively in normal physiologic functions. Compelling evidence, however, suggests that Nox4 plays a critical role in fibrosis, as well as a host of pathologies and diseases. These considerations led to a search for novel, small molecule inhibitors of this important enzyme. Ultimately, a series of novel tertiary sulfonylureas (23-25) was designed using pharmacophore modeling, synthesized, and evaluated for inhibition of Nox4-dependent signaling.

Indexed as

Drug DesignCell LineCell SurvivalEnzyme InhibitorsHumansNADPH Oxidase 4Reactive Oxygen SpeciesSignal TransductionSulfonylurea CompoundsEnzyme InhibitorsNADPH Oxidase 4Reactive Oxygen SpeciesSulfonylurea CompoundsMolecular modelingNADPH oxidasesNox4Pharmacophore developmentReactive oxygen species (ROS)

Identifiers

PMID29426628
PMCPMC5895456

What OpenQuestion holds

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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.