Evidence map›Paper›PMID 32113844›Full record

ArticleBioorganic & medicinal chemistry2020

Ligand-based design of GLUT inhibitors as potential antitumor agents.

Suliman Almahmoud, Wei Jin, Liying Geng, Jing Wang, Xiaofang Wang, Jonathan L Vennerstrom, Haizhen A Zhong

Open access · greenAbstract read
In one paragraph

Article in Bioorganic & medicinal chemistry, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.8field-weighted citation impact, top 35% 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

8 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Direct targeting of GLUT1 in cancer: A decade of inhibitor discovery and medicinal chemistry insights.Medicinal chemistry research : an international journal for rapid communications on design and mechanisms of action of biologically active agents · 2026
    Review
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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

7 authors at 3 institutions in 1 country.

Suliman AlmahmoudDepartment of Pharmaceutical Sciences, College of Pharmacy, University of Nebraska Medical Center, Omaha, Nebraska 68198-6125, United States.
Wei JinDepartment of Cancer Biology and Genetics, College of Medicine, The Ohio State University, 460 W 12(th) Ave., Columbus, OH 43210, United States.
Liying GengDepartment of Cancer Biology and Genetics, College of Medicine, The Ohio State University, 460 W 12(th) Ave., Columbus, OH 43210, United States.
Jing WangDepartment of Cancer Biology and Genetics, College of Medicine, The Ohio State University, 460 W 12(th) Ave., Columbus, OH 43210, United States.
Xiaofang WangDepartment of Pharmaceutical Sciences, College of Pharmacy, University of Nebraska Medical Center, Omaha, Nebraska 68198-6125, United States.
Jonathan L VennerstromDepartment of Pharmaceutical Sciences, College of Pharmacy, University of Nebraska Medical Center, Omaha, Nebraska 68198-6125, United States.
Haizhen A ZhongDepartment of Chemistry, University of Nebraska at Omaha, 6001 Dodge Street, Omaha, Nebraska 68182, United States. Electronic address: hzhong@unomaha.edu.
Nebraska Medical Center · USUniversity of Nebraska at Omaha · USUniversity of Nebraska Medical Center · US

Funding

The Functional Role of GRM3 in Colon CancerR01CA215389 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI WANG, JING · 2017 to 2022
$1.8M
NCI NIH HHS R01 CA215389
6 · The paper itself

Abstract

Glucose transporters (GLUTs) regulate glucose uptake and are often overexpressed in several human tumors. To identify new chemotypes targeting GLUT1, we built a pharmacophore model and searched against a NCI compound database. Sixteen hit molecules with good docking scores were screened for GLUT1 inhibition and antiproliferative activities. From these, we identified that compounds 2, 5, 6 and 13 inhibited the cell viability in a dose-dependent manner and that the IC

Indexed as

Drug DesignAntineoplastic AgentsCell ProliferationDatabases, ChemicalGlucose Transporter Type 1HCT116 CellsHumansLigandsMolecular Docking SimulationProtein BindingStructure-Activity RelationshipAntineoplastic AgentsGlucose Transporter Type 1LigandsAnticancerDockingGlucoseGLUT1Pharmacophore

Identifiers

PMID32113844
PMCPMC11491113
OpenAlexW3006707022

What OpenQuestion holds

Textmetadata
LicenceTDM
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.