Evidence map›Paper›PMID 37259423›Full record

ArticlePharmaceuticals (Basel, Switzerland)2023

In Silico and In Vitro Screening of Serine Racemase Agonist and In Vivo Efficacy on Alzheimer's Disease

Chih-Hao Lu, Hao-Teng Chang, Lee-Fen Hsu, Ming-Hsueh Lee, Jack Cheng, Dong Chuan Wu, Wei-Yong Lin

Open access · goldAbstract read
In one paragraph

Article in Pharmaceuticals (Basel, Switzerland), 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
0.9field-weighted citation impact, top 27% 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

5 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. 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 4 institutions in 1 country.

Chih-Hao LuInstitute of Bioinformatics and Systems Biology, National Yang Ming Chiao Tung University, Hsinchu 300093, Taiwan.ORCID 0000-0002-8363-6244
Hao-Teng ChangGraduate Institute of Biomedical Sciences, China Medical University, Taichung 40402, Taiwan.
Lee-Fen HsuDepartment of Respiratory Care, Chang Gung University of Science and Technology, Puzi City 613, Chiayi County, Taiwan.
Ming-Hsueh LeeDivision of Neurosurgery, Department of Surgery, Chang Gung Memorial Hospital, Puzi City 613, Chiayi County, Taiwan.
Jack ChengGraduate Institute of Integrated Medicine, China Medical University, Taichung 40402, Taiwan.
Dong Chuan WuGraduate Institute of Biomedical Sciences, China Medical University, Taichung 40402, Taiwan.
Wei-Yong LinGraduate Institute of Integrated Medicine, China Medical University, Taichung 40402, Taiwan.ORCID 0000-0002-8443-6180
China Medical University · TWChang Gung University of Science and Technology · TWChiayi Chang Gung Memorial Hospital · TWNational Yang Ming Chiao Tung University · TW

Funding

Chang Gung Memorial Hospital CMRPF6H0091Chang Gung Memorial Hospital CMRPF6L0011Chang Gung Memorial Hospital ZRRPF6L0011China Medical University CMU108-MF-61China Medical University CMU109-MF-110China Medical University CMU110-MF-92China Medical University CMU110-MF-96China Medical University CMU111-MF-65China Medical University Hospital DMR-111-147China Medical University Hospital DMR-112-125National Science and Technology Council, Taiwan MOST 108-2320-B-039-031-MY3National Science and Technology Council, Taiwan MOST 111-2314-B-039-017-MY3National Science and Technology Council, Taiwan MOST 111-2320-B-039-032
6 · The paper itself

Abstract

The NMDA receptor hypofunction has been implicated in schizophrenia, memory impairment, and Alzheimer's disease. Modulating the abundance of D-serine, a co-agonist of the NMDA receptor, is a strategy to treat symptoms of the NMDA receptor hypofunction. In contrast to D-amino acid oxidase (DAAO) inhibitors, which aim at decreasing the loss of D-serine, this study tried to identify serine racemase (SRR) agonists, which boost the conversion of L-serine to D-serine. We used holo and apo structures of human SRR for the molecular docking against the National Cancer Institute (NCI) and ZINC compound databases and validated their efficacy by in vitro SRR activity assay. We identified NSC294149 (2-amino-3-(3-nitroimidazo[1,2-a]pyridin-2-yl)sulfanylpropanoic acid) as a potential SRR agonist and confirmed its amelioration of the hazard ratio of survival of the AD model of fruit fly (

Indexed as

drug developmentD-serineNMDA receptor hypofunctionserine racemase

Identifiers

PMID37259423
PMCPMC9962741
OpenAlexW4320729135

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.