Evidence map›Paper›PMID 31244110›Full record

ArticleJournal of medicinal chemistry2019

Structure-Based Discovery of M-89 as a Highly Potent Inhibitor of the Menin-Mixed Lineage Leukemia (Menin-MLL) Protein-Protein Interaction.

Angelo Aguilar, Ke Zheng, Tianfeng Xu, Shilin Xu, Liyue Huang, Ester Fernandez-Salas, Liu Liu, Denzil Bernard, Kaitlin P Harvey, Caroline Foster and 6 more

Abstract read
In one paragraph

Article in Journal of medicinal chemistry, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Review
  2. Review
  3. Distinct Responses to Menin Inhibition and Synergy with DOT1L Inhibition inInternational journal of molecular sciences · 2024
    Article
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  6. Article
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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

16 authors.

Angelo Aguilar
Ke Zheng
Tianfeng Xu
Shilin Xu
Liyue Huang
Ester Fernandez-Salas
Liu Liu
Denzil Bernard
Kaitlin P Harvey
Caroline Foster
Donna McEachern
Jeanne Stuckey
Krishnapriya Chinnaswamy
James Delproposto
Jeff W Kampf

Funding

XenograftP30CA046592 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI THEODORE S LAWRENCE · 1988 to 2026
$178.2M
Targeting the menin-MLL1 complex for new therapeuticsR01CA208267 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI WANG, SHAOMENG · 2018 to 2022
$3.2M
NCI NIH HHS P30 CA046592NCI NIH HHS R01 CA208267
6 · The paper itself

Abstract

Inhibition of the menin-mixed lineage leukemia (MLL) protein-protein interaction is a promising new therapeutic strategy for the treatment of acute leukemia carrying MLL fusion (MLL leukemia). We describe herein our structure-based design, synthesis, and evaluation of a new class of small-molecule inhibitors of the menin-MLL interaction (hereafter called menin inhibitors). Our efforts have resulted in the discovery of highly potent menin inhibitors, as exemplified by compound

Indexed as

Acute DiseaseCell Line, TumorCell ProliferationCrystallography, X-RayDrug DiscoveryHL-60 CellsHumansLeukemia, MyeloidModels, ChemicalMolecular StructureMyeloid-Lymphoid Leukemia ProteinProtein BindingProto-Oncogene ProteinsSmall Molecule LibrariesStructure-Activity RelationshipMEN1 protein, humanMyeloid-Lymphoid Leukemia ProteinProto-Oncogene ProteinsSmall Molecule Libraries

Identifiers

PMID31244110
PMCPMC7057177

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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.