Evidence map›Paper›PMID 37312852›Full record

ArticleACS medicinal chemistry letters2023

Design, Synthesis, and Structure-Activity Relationships of Biaryl Anilines as Subtype-Selective PPAR-alpha Agonists.

Julia J Lee, Ziwei Hu, Yuhong Anna Wang, Dinesh Nath, Wentao Liang, Yi Cui, Jian-Xing Ma, Adam S Duerfeldt

Abstract read
In one paragraph

Article in ACS medicinal chemistry letters, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

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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.

Julia J LeeDepartment of Medicinal Chemistry, College of Pharmacy, University of Minnesota, Minneapolis, Minnesota 55455, United States.
Ziwei HuDepartment of Medicinal Chemistry, College of Pharmacy, University of Minnesota, Minneapolis, Minnesota 55455, United States.
Yuhong Anna WangDepartment of Physiology, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma 73104, United States.
Dinesh NathDepartment of Chemistry and Biochemistry, University of Oklahoma, Norman, Oklahoma 73019, United States.
Wentao LiangDepartment of Biochemistry, Wake Forest School of Medicine, Winston-Salem, North Carolina 27101, United States.ORCID https://orcid.org/0000-0002-0609-6280
Yi CuiDepartment of Biochemistry, Wake Forest School of Medicine, Winston-Salem, North Carolina 27101, United States.
Jian-Xing MaDepartment of Biochemistry, Wake Forest School of Medicine, Winston-Salem, North Carolina 27101, United States.
Adam S DuerfeldtDepartment of Medicinal Chemistry, College of Pharmacy, University of Minnesota, Minneapolis, Minnesota 55455, United States.ORCID https://orcid.org/0000-0002-3130-9890

Funding

A Novel Pathogenic Pathway for Diabetic KeratopathyR01EY028949 · NEI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI Dimitrios Karamichos, Jian-Xing Jay Ma · 2018 to 2026
$2.2M
Small Molecule PPAR-alpha Agonism as a Novel Approach to Treat Eye Vascular DiseasesR01EY030472 · NEI · UNIVERSITY OF OKLAHOMA · PI DUERFELDT, ADAM SCOTT · 2020 to 2024
$2.1M
cGAS-STING signaling in diabetic retinopathyR01EY033330 · NEI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI Jian-Xing Jay Ma, Yusuke Takahashi · 2022 to 2026
$1.9M
NEI NIH HHS R01 EY028949NEI NIH HHS R01 EY030472NEI NIH HHS R01 EY033330
6 · The paper itself

Abstract

The role of peroxisome proliferator-activated receptor alpha (PPARα) in retinal biology is clarifying, and evidence demonstrates that novel PPARα agonists hold promising therapeutic utility for diseases like diabetic retinopathy and age-related macular degeneration. Herein, we disclose the design and initial structure-activity relationships for a new biaryl aniline PPARα agonistic chemotype. Notably, this series exhibits subtype selectivity for PPARα over other isoforms, a phenomenon postulated to be due to the unique benzoic acid headgroup. This biphenyl aniline series is sensitive to B-ring functionalization but allows isosteric replacement, and provides an opportunity for C-ring extension. From this series,

Identifiers

PMID37312852
PMCPMC10258832

What OpenQuestion holds

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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.