Evidence map›Paper›PMID 26187705›Full record

ArticleBioorganic & medicinal chemistry letters2015

Second generation 2-aminoimidazole based advanced glycation end product inhibitors and breakers.

Robert E Furlani, Mike A Richardson, Brendan K Podell, David F Ackart, Jessica D Haugen, Roberta J Melander, Randall J Basaraba, Christian Melander

Abstract read
In one paragraph

Article in Bioorganic & medicinal chemistry letters, 2015. 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
1.3field-weighted citation impact, top 22% 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, 15 citations in OpenAlex.

  1. Article
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  4. Isosamidin fromAntioxidants (Basel, Switzerland) · 2020
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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

8 authors at 2 institutions in 1 country.

Robert E FurlaniDepartment of Chemistry, North Carolina State University, Raleigh, NC 27695, USA.
Mike A RichardsonDepartment of Microbiology, Immunology and Pathology, Mycobacteria Research Laboratories, Colorado State University, Fort Collins, CO 80524, USA.
Brendan K PodellDepartment of Microbiology, Immunology and Pathology, Mycobacteria Research Laboratories, Colorado State University, Fort Collins, CO 80524, USA.
David F AckartDepartment of Microbiology, Immunology and Pathology, Mycobacteria Research Laboratories, Colorado State University, Fort Collins, CO 80524, USA.
Jessica D HaugenDepartment of Microbiology, Immunology and Pathology, Mycobacteria Research Laboratories, Colorado State University, Fort Collins, CO 80524, USA.
Roberta J MelanderDepartment of Chemistry, North Carolina State University, Raleigh, NC 27695, USA.
Randall J BasarabaDepartment of Microbiology, Immunology and Pathology, Mycobacteria Research Laboratories, Colorado State University, Fort Collins, CO 80524, USA.
Christian MelanderDepartment of Chemistry, North Carolina State University, Raleigh, NC 27695, USA.
Colorado State University · USNorth Carolina State University · US

Funding

Disrupting Biofilm Formation to Improve TB Drug TreatmentR01AI106733 · NIAID · COLORADO STATE UNIVERSITY · PI BASARABA, RANDALL J · 2013 to 2017
$2.3M
Mechanisms of Diabetic Susceptibility to TuberculosisK01OD016997 · OD · COLORADO STATE UNIVERSITY · PI PODELL, BRENDAN · 2014 to 2018
$615k
Therapeutic Restoration of Metabolic Homeostasis During Active TBR21AI107254 · NIAID · COLORADO STATE UNIVERSITY · PI BASARABA, RANDALL J · 2014 to 2015
$409k
NIAID NIH HHS 1R01AI106733-01NIAID NIH HHS R01 AI106733NIAID NIH HHS R21 AI107254NIAID NIH HHS R21AI107254-02NIH HHS 1K01OD016997NIH HHS K01 OD016997
6 · The paper itself

Abstract

The formation of advanced glycation end-products (AGE) as a result of the action of reducing sugars on host macromolecules plays a role in increased morbidity of diabetic patients. There are currently no clinically available therapeutics for the prevention or eradication of AGEs. Following our previous identification of 2-aminoimidazole (2-AI) based AGE inhibitors and breakers, we now report the use of a rapid, scalable, two-step procedure to access a second generation of 2-AI based anti-AGE compounds from commercially available amino acids. Several second generation compounds exhibit increased AGE inhibition and breaking activty compared to the first generation compounds and to the known AGE inhibitor aminoguanidine.

Indexed as

Glycation End Products, AdvancedImidazolesMolecular StructureStructure-Activity Relationship2-aminoimidazoleGlycation End Products, AdvancedImidazoles2-AminoimidazoleAdvanced glycation end-product (AGE)AkaboriDiabetes

Identifiers

PMID26187705
PMCPMC4607637
OpenAlexW1830322222

What OpenQuestion holds

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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.