Evidence map›Paper›PMID 39417235›Full record

ArticleJournal of medicinal chemistry2024

Metal-Free CO Prodrugs Activated by Molecular Oxygen Protect against Doxorubicin-Induced Cardiomyopathy in Mice.

Xiaoxiao Yang, Wen Lu, Rodrigo W Alves de Souza, Qiyue Mao, Dipak Baram, Ravi Tripathi, Gangli Wang, Leo E Otterbein, Binghe Wang

Abstract read
In one paragraph

Article in Journal of medicinal chemistry, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Heme Metabolism-Derived Carbon Monoxide Regulates Skeletal Muscle Function.Journal of cachexia, sarcopenia and muscle · 2026
    Article
  2. Review
  3. Article
  4. Review
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.

Xiaoxiao YangChemistry Department, Center for Diagnostics and Therapeutics, Georgia State University, Atlanta, Georgia 30303, United States.ORCID 0000-0001-9895-9559
Wen LuChemistry Department, Center for Diagnostics and Therapeutics, Georgia State University, Atlanta, Georgia 30303, United States.
Rodrigo W Alves de SouzaDepartment of Surgery, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts 02215, United States.
Qiyue MaoChemistry Department, Center for Diagnostics and Therapeutics, Georgia State University, Atlanta, Georgia 30303, United States.
Dipak BaramChemistry Department, Center for Diagnostics and Therapeutics, Georgia State University, Atlanta, Georgia 30303, United States.
Ravi TripathiChemistry Department, Center for Diagnostics and Therapeutics, Georgia State University, Atlanta, Georgia 30303, United States.
Gangli WangChemistry Department, Center for Diagnostics and Therapeutics, Georgia State University, Atlanta, Georgia 30303, United States.ORCID 0000-0001-9204-7807
Leo E OtterbeinDepartment of Surgery, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts 02215, United States.
Binghe WangChemistry Department, Center for Diagnostics and Therapeutics, Georgia State University, Atlanta, Georgia 30303, United States.ORCID 0000-0002-2200-5270

Funding

Examining Carbon Monoxide to Treat Inflammatory Conditions using Experimental Colitis ModelsR01DK119202 · NIDDK · GEORGIA STATE UNIVERSITY · PI OTTERBEIN, LEO E, TAN, CHALET · 2019 to 2023
$3.6M
Early-Stage Preclinical Validation of Carbon Monoxide Prodrugs for Acute Kidney InjuryR01DK128823 · NIDDK · GEORGIA STATE UNIVERSITY · PI LEO E OTTERBEIN, Binghe Wang · 2022 to 2026
$3.5M
A Single Entity Method for Controlled Nucleation and Crystal GrowthR01GM151275 · NIGMS · GEORGIA STATE UNIVERSITY · PI Gangli Wang · 2023 to 2026
$1.3M
A Xevo G2-XS Mass Spectrometer Equipped with an Acquity UPLC as a Workhorse Instrument to Replace a 15-year old Waters Q-TOF MicroS10OD026764 · OD · GEORGIA STATE UNIVERSITY · PI WANG, SIMING · 2020 to 2020
$428k
NIDDK NIH HHS R01 DK119202NIDDK NIH HHS R01 DK128823NIGMS NIH HHS R01 GM151275NIH HHS S10 OD026764
6 · The paper itself

Abstract

Carbon monoxide has been extensively studied for its various therapeutic activities in cell cultures and animal models. Great efforts have been made to develop noninhalational approaches for easy and controlled CO delivery. Herein, we introduce a novel metal-free CO prodrug approach that releases CO under near-physiological conditions. CO from the quinone-derived CO prodrugs is initiated by general acid/base-catalyzed tautomerization followed by oxidation by molecular oxygen to form the key norbornadienone intermediate, leading to cheletropic CO release only in an aerobic environment. Representative CO prodrug analog

Indexed as

Carbon MonoxideCardiomyopathiesDoxorubicinOxygenProdrugsAnimalsHeme Oxygenase-1MaleMiceMice, Inbred C57BLMyocytes, CardiacRAW 264.7 CellsCarbon MonoxideDoxorubicinHeme Oxygenase-1OxygenProdrugs

Identifiers

PMID39417235
PMCPMC11571113

What OpenQuestion holds

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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.