Evidence map›Paper›PMID 26510670›Full record

ArticleBioorganic & medicinal chemistry letters2015

Ethynylphenyl carbonates and carbamates as dual-action acetylcholinesterase inhibitors and anti-inflammatory agents.

Jaya Saxena, David Meloni, Mou-Tuan Huang, Diane E Heck, Jeffrey D Laskin, Ned D Heindel, Sherri C Young

Open access · greenAbstract 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 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.1field-weighted citation impact, top 21% 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

2 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. 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

7 authors at 5 institutions in 1 country.

Jaya SaxenaDepartment of Chemistry, Lehigh University, Bethlehem, PA 18015, United States.
David MeloniDepartment of Chemistry, Lehigh University, Bethlehem, PA 18015, United States; Incyte Corporation, Wilmington, DE 19803, United States.
Mou-Tuan HuangDepartment of Chemical Biology, Rutgers University, Piscataway, NJ 08854, United States.
Diane E HeckDepartment of Environmental Health Science, New York Medical College, Valhalla, NY 10595, United States.
Jeffrey D LaskinDepartment of Environmental and Occupational Medicine, Rutgers University, Piscataway, NJ 08854, United States.
Ned D HeindelDepartment of Chemistry, Lehigh University, Bethlehem, PA 18015, United States.
Sherri C YoungDepartment of Chemistry, Lehigh University, Bethlehem, PA 18015, United States; Department of Chemistry, Muhlenberg College, Allentown, PA 18104, United States. Electronic address: young@muhlenberg.edu.
Lehigh University · USRutgers, The State University of New Jersey · USIncyte (United States) · USMuhlenberg College · USNew York Medical College · US

Funding

UMDNJ/Rutgers University CounterACT Research Center of ExcellenceU54AR055073 · NIAMS · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI HECK, DIANE E · 2006 to 2024
$71.4M
NIAMS NIH HHS U54 AR055073NIAMS NIH HHS U54AR055073
6 · The paper itself

Abstract

Novel ethynylphenyl carbonates and carbamates containing carbon- and silicon-based choline mimics were synthesized from their respective phenol and aniline precursors and screened for anticholinesterase and anti-inflammatory activities. All molecules were micromolar inhibitors of acetylcholinesterase (AChE), with IC50s of 28-86 μM; the carbamates were two-fold more potent than the carbonates. Two of the most potent AChE inhibitors suppressed 12-O-tetradecanoylphorbol-13-acetate (TPA)-induced inflammation by 40%. Furthermore, these molecules have physicochemical properties in the range of other CNS drugs. These molecules have the potential to treat inflammation; they could also dually target Alzheimer's disease through restoration of cholinergic balance and inflammation suppression.

Indexed as

AcetylcholinesteraseAnti-Inflammatory AgentsCarbamatesCarbonatesCholinesterase InhibitorsHumansInhibitory Concentration 50Molecular StructureAcetylcholinesteraseAnti-Inflammatory AgentsCarbamatesCarbonatesCholinesterase InhibitorsAcetylcholinesterase inhibitorsAlzheimer’s diseaseAnti-inflammatory drugsCarbamatesCarbonates

Identifiers

PMID26510670
PMCPMC4700827
OpenAlexW1859652568

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.