Evidence map›Paper›PMID 40709844›Full record

ArticleJournal of medicinal chemistry2025

Design, Synthesis, and Cellular Characterization of a New Class of IPMK Kinase Inhibitors.

Yubai Zhou, Pratima Chapagain, Desmarini Desmarini, Dilipkumar Uredi, Michael A Stashko, Hundaol Huluka, Lucia E Rameh, Julianne T Djordjevic, Raymond D Blind, Xiaodong Wang

Abstract read
In one paragraph

Article in Journal of medicinal chemistry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Structural Rationalization of IPMK Inhibitor Potency.Journal of medicinal chemistry · 2025
    Article
  6. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Yubai ZhouCenter for Integrative Chemical Biology and Drug Discovery, Division of Chemical Biology and Medicinal Chemistry, Eshelman School of Pharmacy, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599, United States.ORCID 0000-0003-3704-283X
Pratima ChapagainDepartment of Medicine, Division of Diabetes, Endocrinology & Metabolism, Vanderbilt University Medical Center, Nashville, Tennessee 37232, United States.
Desmarini DesmariniCentre for Infectious Diseases and Microbiology, The Westmead Institute for Medical Research, Westmead NSW 2145, Australia.
Dilipkumar UrediCenter for Integrative Chemical Biology and Drug Discovery, Division of Chemical Biology and Medicinal Chemistry, Eshelman School of Pharmacy, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599, United States.
Michael A StashkoCenter for Integrative Chemical Biology and Drug Discovery, Division of Chemical Biology and Medicinal Chemistry, Eshelman School of Pharmacy, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599, United States.
Hundaol HulukaDepartment of Medicine, Division of Diabetes, Endocrinology & Metabolism, Vanderbilt University Medical Center, Nashville, Tennessee 37232, United States.
Lucia E RamehDepartment of Medicine, Division of Diabetes, Endocrinology & Metabolism, Vanderbilt University Medical Center, Nashville, Tennessee 37232, United States.
Julianne T DjordjevicCentre for Infectious Diseases and Microbiology, The Westmead Institute for Medical Research, Westmead NSW 2145, Australia.ORCID 0000-0003-4207-4115
Raymond D BlindDepartment of Medicine, Division of Diabetes, Endocrinology & Metabolism, Vanderbilt University Medical Center, Nashville, Tennessee 37232, United States.
Xiaodong WangCenter for Integrative Chemical Biology and Drug Discovery, Division of Chemical Biology and Medicinal Chemistry, Eshelman School of Pharmacy, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599, United States.ORCID 0000-0003-3293-7538

Funding

Structure and function of phospholipids and inositol phosphates in the nucleus.R35GM156389 · NIGMS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Raymond Daniel Blind · 2025 to 2026
$1.4M
Unconventional regulation of mTORC1 signaling by inositol phosphate: implications for nutrient-induced premature agingR21AG071975 · NIA · VANDERBILT UNIVERSITY MEDICAL CENTER · PI BLIND, RAYMOND DANIEL, BURKEWITZ, KRISTOPHER · 2022 to 2023
$483k
NIA NIH HHS R21 AG071975NIGMS NIH HHS R35 GM156389
6 · The paper itself

Abstract

The kinase activity of human inositol phosphate multikinase (IPMK) is required for the synthesis of higher-order inositol phosphate signaling molecules, regulation of gene expression, and control of the cell cycle. Here, we report a novel series of highly potent IPMK inhibitors. The first-generation IPMK inhibitor

Indexed as

Antineoplastic AgentsDrug DesignPhosphotransferases (Alcohol Group Acceptor)Protein Kinase InhibitorsAnimalsCell Line, TumorCell ProliferationHumansInositol PhosphatesStructure-Activity RelationshipAntineoplastic AgentsInositol PhosphatesPhosphotransferases (Alcohol Group Acceptor)Protein Kinase Inhibitors

Identifiers

PMID40709844
PMCPMC12362615

What Socratic 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 Socratic graph.