Cited by 76Redox biology and oxidative stressNitric Oxide and Endothelin EffectsNeutrophil, Myeloperoxidase and Oxidative Mechanisms

Off-target thiol alkylation by the NADPH oxidase inhibitor 3-benzyl-7-(2-benzoxazolyl)thio-1,2,3-triazolo[4,5-d]pyrimidine (VAS2870)

Open access
Sun, Qi-An, Hess, Douglas T., Wang, Benlian, Miyagi, Masaru, Stamler, Jonathan S.·2012·Free Radical Biology and Medicine

Abstract

Specific inhibitors of the production of reactive oxygen species (ROS) by the NADPH oxidases (Nox's) are potentially important therapeutic agents in the wide range of human diseases that are characterized by excessive ROS production. It has been proposed that VAS2870 (3-benzyl-7-(2-benzoxazolyl)thio-1,2,3- triazolo[4,5-d]pyrimidine), identified as an inhibitor of Nox2 by small-molecule screening, may serve as an example of such an agent. Here we show that VAS2870 inhibits ROS production in the sarcoplasmic reticulum (SR) of mammalian skeletal muscle, previously identified with Nox4, and thereby abrogates O(2)-coupled redox regulation of the ryanodine receptor-Ca(2+) channel (RyR1). However, we also find that VAS2870 modifies directly identified cysteine thiols within RyR1. Mass spectrometric analysis of RyR1 exposed in situ to VAS2870 and of VAS2870-treated glutathione indicated that thiol modification is through alkylation by the benzyltriazolopyrimidine moiety of VAS2870. Thus, VAS2870 exerts significant off-target effects, and thiol alkylation by VAS2870 (and closely related Nox inhibitors) may in fact replicate some of the effects of ROS on cellular thiol redox status. In addition, we show that SR-localized Nox4 is inhibited by other thiol-alkylating agents, consistent with a causal role for cysteine modification in the inhibition of ROS production by VAS2870.

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1016/j.freeradbiomed.2012.02.046

Cites

26 of 26 references verified0 citation errors · 0 not checkable

Statistics

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

  • eNOS deletion has limited effects on mouse blood pressure and vasodilation, as adaptive processes increase production of nNOS and prostaglandins.

    “eNOS deletion has some limited effects on mouse blood pressure and vasodilation, as adaptive processes increase the production of nNOS and prostaglandins”

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Cites

Flagged first, then by citations

Cited by

Sorted by citations

Authors
Sun, Q.-A., Hess, D. T., Wang, B., Miyagi, M., & Stamler, J. S.
Affiliations
  • Case Western Reserve University (US)
  • University Hospitals of Cleveland (US)
Corresponding author
Stamler, Jonathan S.
Venue
Free Radical Biology and Medicine
Publisher
Elsevier BV
Published
2012-05
Volume
52
Issue
9
Pages
1897-1902
ISSN
0891-5849 (ISSN-L)
OpenAlex
W2091077982
Cited by
76
References
26
Citations by year
2026: 4 · 2025: 2 · 2024: 2 · 2023: 4 · 2022: 4 · 2021: 4 · 2020: 9 · 2019: 6 · 2018: 3 · 2017: 8 · 2016: 7 · 2015: 5 · 2014: 8 · 2013: 5 · 2012: 5
FWCI
2.96
Type
journal article
Language
en
Open access
Locations
  • Free Radical Biology and Medicine (publishedVersion)
  • PubMed (publishedVersion)
  • Europe PMC (PubMed Central) (acceptedVersion)
  • PubMed Central (acceptedVersion)
Funders
National Heart, Lung, and Blood Institute (R01 HL0591130, R01HL059130)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Redox biology and oxidative stress
  • Health Sciences › Medicine › Physiology › Nitric Oxide and Endothelin Effects
  • Life Sciences › Immunology and Microbiology › Immunology › Neutrophil, Myeloperoxidase and Oxidative Mechanisms
Keywords
VAS2870, NADPH oxidase inhibitors, off-target effects, thiol alkylation, cysteine modification, reactive oxygen species, NOX4, sarcoplasmic reticulum, skeletal muscle, RyR1, glutathione, redox regulation
MeSH terms
Alkylation, Benzoxazoles, Enzyme Inhibitors, Sulfhydryl Compounds, Triazoles, NADPH Oxidases

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review