Evidence map›Paper›PMID 29034580›Full record

ArticleChemical biology & drug design2018

Selective inhibition of TRPM2 channel by two novel synthesized ADPR analogues.

Xiao Luo, Meng Li, Kaiyu Zhan, Wei Yang, Lihe Zhang, KeWei Wang, Peilin Yu, Liangren Zhang

Open access · hybridAbstract read
In one paragraph

Article in Chemical biology & drug design, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.6field-weighted citation impact, top 11% 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

25 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Review
  6. [Advances in the development of transient receptor potential melastatin 2 channel inhibitors].Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences · 2025
    Review
  7. Article
  8. Article
  9. TRPM2 Channels: A Potential Therapeutic Target in Melanoma?International journal of molecular sciences · 2023
    Review
  10. Review
  11. Review
  12. Review
  13. The Role of TRPM2 in Endothelial Function and Dysfunction.International journal of molecular sciences · 2021
    Review
  14. Review
  15. Article
  16. Review
  17. Article
  18. Review
  19. Review
  20. 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

8 authors at 3 institutions in 1 country.

Xiao LuoState Key Laboratory of Natural and Biomimetic Drugs, Peking University, Beijing, China.ORCID 0000-0002-4708-1341
Meng LiDepartment of Neurobiology, Neuroscience Research Institute, Peking University Health Science Center, Peking University School of Pharmaceutical Sciences, Beijing, China.
Kaiyu ZhanDepartment of Neurobiology, Zhejiang University School of Medicine, Hangzhou, Zhejiang, China.
Wei YangDepartment of Neurobiology, Zhejiang University School of Medicine, Hangzhou, Zhejiang, China.
Lihe ZhangState Key Laboratory of Natural and Biomimetic Drugs, Peking University, Beijing, China.
KeWei WangDepartment of Neurobiology, Neuroscience Research Institute, Peking University Health Science Center, Peking University School of Pharmaceutical Sciences, Beijing, China.
Peilin YuDepartment of Toxicology, School of Public Health, Zhejiang University, Hangzhou, Zhejiang, China.
Liangren ZhangState Key Laboratory of Natural and Biomimetic Drugs, Peking University, Beijing, China.
Peking University · CNQingdao University · CNZhejiang University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Transient receptor potential melastatin-2 (TRPM2) channel critical for monitoring internal body temperature is implicated in the pathological processes such as neurodegeneration. However, lacking selective and potent TRPM2 inhibitors impedes investigation and validation of the channel as a drug target. To discover novel and selective TRPM2 inhibitors, a series of adenosine 5'-diphosphoribose analogues were synthesized, and their activities and selectivity were evaluated. Whole-cell patch-clamp recordings were employed for screen and evaluation of synthesized compounds. Two compounds, 7i and 8a, were identified as TRPM2 inhibitors with IC

Indexed as

Adenosine Diphosphate RiboseCalciumHEK293 CellsHumansInhibitory Concentration 50Patch-Clamp TechniquesProtein IsoformsStructure-Activity RelationshipTRPM Cation ChannelsAdenosine Diphosphate RiboseCalciumProtein IsoformsTRPM2 protein, humanTRPM Cation ChannelsADPR analoguesinhibitorselectivityTRP channelsTRPM2

Identifiers

PMID29034580
PMCPMC5813235
OpenAlexW2761493792

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.