Evidence map›Paper›PMID 30344916›Full record

ArticleACS medicinal chemistry letters2018

Development of Hybrid Phospholipid Mimics as Effective Agonists for Liver Receptor Homologue-1.

Autumn R Flynn, Suzanne G Mays, Eric A Ortlund, Nathan T Jui

Abstract read
In one paragraph

Article in ACS medicinal chemistry letters, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Article
  2. Review
  3. Fragment-Based Discovery of Drug-like LRH-1 Agonists.ACS medicinal chemistry letters · 2025
    Article
  4. Fatty Acid Mimetic Fragments as Liver Receptor Homologue-1 Modulators.ACS pharmacology & translational science · 2025
    Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. 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

4 authors.

Autumn R FlynnDepartment of Chemistry, Department of Biochemistry, and Winship Cancer Institute, Emory University, Atlanta, Georgia 30322, United States.
Suzanne G MaysDepartment of Chemistry, Department of Biochemistry, and Winship Cancer Institute, Emory University, Atlanta, Georgia 30322, United States.
Eric A OrtlundDepartment of Chemistry, Department of Biochemistry, and Winship Cancer Institute, Emory University, Atlanta, Georgia 30322, United States.
Nathan T JuiDepartment of Chemistry, Department of Biochemistry, and Winship Cancer Institute, Emory University, Atlanta, Georgia 30322, United States.

Funding

Graduate Training in the Pharmacological StudiesT32GM008602 · NIGMS · EMORY UNIVERSITY · PI HALL, RANDY A. · 1996 to 2021
$5.1M
Targeting the orphan nuclear receptor LRH-1 with small moleculesR01DK115213 · NIDDK · EMORY UNIVERSITY · PI John Winter Calvert, Eric A Ortlund · 2017 to 2026
$4.6M
Targeting LRH-1 - Phospholipid Signaling in Metabolic PathwaysR01DK095750 · NIDDK · EMORY UNIVERSITY · PI ORTLUND, ERIC A · 2012 to 2016
$1.7M
A pilot study to target out-of-dialysis-unit versus dialysis-unit blood pressureR21DK114213 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BANSAL, NISHA, HSU, CHI-YUAN · 2017 to 2018
$456k
Regulation of LRH-1 by small moleculesF31DK111171 · NIDDK · EMORY UNIVERSITY · PI MAYS, SUZANNE GILCHRIST · 2016 to 2018
$116k
NIDDK NIH HHS F31 DK111171NIDDK NIH HHS R01 DK095750NIDDK NIH HHS R01 DK115213NIDDK NIH HHS R21 DK114213NIGMS NIH HHS T32 GM008602
6 · The paper itself

Abstract

The orphan nuclear receptor Liver Receptor Homologue-1 (LRH-1) is an emerging drug target for metabolic disorders. The most effective known LRH-1 modulators are phospholipids or synthetic hexahydropentalene compounds. While both classes have micromolar efficacy, they target different portions of the ligand binding pocket and activate LRH-1 through different mechanisms. Guided by crystallographic data, we combined aspects of both ligand classes into a single scaffold, resulting in the most potent and efficacious LRH-1 agonists to date.

Identifiers

PMID30344916
PMCPMC6187417

What OpenQuestion holds

Textmetadata
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Registered trials

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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.