Evidence map›Paper›PMID 35506893›Full record

ArticleOrganic & biomolecular chemistry2022

Synthetic studies on the indane SHIP1 agonist AQX-1125.

Otto M Dungan, Shawn Dormann, Sandra Fernandes, Brian C Duffy, Daniel G Effiong, William G Kerr, John D Chisholm

Open access · greenAbstract read
In one paragraph

Article in Organic & biomolecular chemistry, 2022. 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
0.2field-weighted citation impact, top 53% 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, 2 citations in OpenAlex.

  1. Article
  2. Molecules (Basel, Switzerland) · 2022
    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

7 authors at 2 institutions in 1 country.

Otto M DunganDepartment of Chemistry, Syracuse University, 1-014 Center for Science and Technology, Syracuse, NY 13244, USA. jdchisho@syr.edu.
Shawn DormannDepartment of Chemistry, Syracuse University, 1-014 Center for Science and Technology, Syracuse, NY 13244, USA. jdchisho@syr.edu.
Sandra FernandesDepartment of Microbiology and Immunology, SUNY Upstate Medical University, Syracuse, NY 13210, USA.ORCID 0000-0003-0919-8925
Brian C DuffyDepartment of Chemistry, Syracuse University, 1-014 Center for Science and Technology, Syracuse, NY 13244, USA. jdchisho@syr.edu.
Daniel G EffiongDepartment of Chemistry, Syracuse University, 1-014 Center for Science and Technology, Syracuse, NY 13244, USA. jdchisho@syr.edu.
William G KerrDepartment of Chemistry, Syracuse University, 1-014 Center for Science and Technology, Syracuse, NY 13244, USA. jdchisho@syr.edu.ORCID 0000-0002-4720-7135
John D ChisholmDepartment of Chemistry, Syracuse University, 1-014 Center for Science and Technology, Syracuse, NY 13244, USA. jdchisho@syr.edu.ORCID 0000-0001-9518-2393
Syracuse University · USSUNY Upstate Medical University · US

Funding

Translating SHIP1 Genetics to Generate a Novel Alzheimers Pharmacologic AgentRF1AG059717 · NIA · UNIVERSITY OF KENTUCKY · PI ESTUS, STEVEN, HUMPHREY, MARY BETH · 2018 to 2019
$3.9M
National Science Foundation CHE1659775NIA NIH HHS RF1 AG059717
6 · The paper itself

Abstract

AQX-1125 is an indane based SHIP1 agonist that has been evaluated in the clinic for the treatment of bladder pain syndrome/interstitial cystitis. To support our own studies on SHIP1 agonists as potential treatments for IBD and Crohn's disease, a new synthetic route to the SHIP1 agonist AQX-1125 has been developed. This sequence utilizes a hydroxy-acid intermediate which allows for ready differentiation of the C6 and C7 positions. The role of the C17 alkene in the biological activity of the system is also investigated, and this functional group is not required for SHIP1 agonist activity. While AQX-1125 shows SHIP1 agonist activity in enzyme assays, it does not show activity in cell based assays similar to other SHIP1 agonists, which limits the utility of this molecule.

Indexed as

CyclohexanolsPhosphoric Monoester HydrolasesIndans4-(4-(aminomethyl)-7a-methyl-1-methylideneoctahydro-1H-inden-5-yl)-3-(hydroxymethyl)-4-methylcyclohexan-1-olCyclohexanolsIndansPhosphoric Monoester Hydrolases

Identifiers

PMID35506893
PMCPMC9153081
OpenAlexW4229025975

What Socratic 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 Socratic graph.