Evidence map›Paper›PMID 32435413›Full record

ArticleACS medicinal chemistry letters2020

Structure-Guided Identification of DNMT3B Inhibitors.

Ana S Newton, John C Faver, Goran Micevic, Viswanathan Muthusamy, Shalley N Kudalkar, Nicole Bertoletti, Karen S Anderson, Marcus W Bosenberg, William L Jorgensen

Abstract read
In one paragraph

Article in ACS medicinal chemistry letters, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Inhibitors of DNA Methylation.Advances in experimental medicine and biology · 2022
    Review
  11. Genomic Variants and Multilevel Regulation ofJournal of cardiovascular development and disease · 2021
    Review
  12. 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

9 authors.

Ana S NewtonDepartment of Chemistry, Yale University, New Haven, Connecticut 06520-8107, United States.
John C FaverDepartment of Chemistry, Yale University, New Haven, Connecticut 06520-8107, United States.
Goran MicevicDepartment of Dermatology, Department of Medicine, Department of Pharmacology, Department of Pathology, and Department of Immunobiology, Yale University School of Medicine, New Haven, Connecticut 06520-8066, United States.
Viswanathan MuthusamyDepartment of Dermatology, Department of Medicine, Department of Pharmacology, Department of Pathology, and Department of Immunobiology, Yale University School of Medicine, New Haven, Connecticut 06520-8066, United States.
Shalley N KudalkarDepartment of Dermatology, Department of Medicine, Department of Pharmacology, Department of Pathology, and Department of Immunobiology, Yale University School of Medicine, New Haven, Connecticut 06520-8066, United States.
Nicole BertolettiDepartment of Dermatology, Department of Medicine, Department of Pharmacology, Department of Pathology, and Department of Immunobiology, Yale University School of Medicine, New Haven, Connecticut 06520-8066, United States.
Karen S AndersonDepartment of Dermatology, Department of Medicine, Department of Pharmacology, Department of Pathology, and Department of Immunobiology, Yale University School of Medicine, New Haven, Connecticut 06520-8066, United States.
Marcus W BosenbergDepartment of Dermatology, Department of Medicine, Department of Pharmacology, Department of Pathology, and Department of Immunobiology, Yale University School of Medicine, New Haven, Connecticut 06520-8066, United States.
William L JorgensenDepartment of Chemistry, Yale University, New Haven, Connecticut 06520-8107, United States.

Funding

POTENTIAL FUNCTIONS FOR WATER PROTEIN INTERACTIONSR01GM032136 · NIGMS · YALE UNIVERSITY · PI JORGENSEN, WILLIAM L. · 1985 to 2023
$8.2M
NIGMS NIH HHS R01 GM032136
6 · The paper itself

Abstract

Methyltransferase 3 beta (DNMT3B) inhibitors that interfere with cancer growth are emerging possibilities for treatment of melanoma. Herein we identify small molecule inhibitors of DNMT3B starting from a homology model based on a DNMT3A crystal structure. Virtual screening by docking led to purchase of 15 compounds, among which 5 were found to inhibit the activity of DNMT3B with IC

Identifiers

PMID32435413
PMCPMC7236258

What OpenQuestion holds

Textmetadata
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.