Evidence map›Paper›PMID 27320659›Full record

ArticleBioorganic & medicinal chemistry2016

Computer-aided drug design guided by hydrogen/deuterium exchange mass spectrometry: A powerful combination for the development of potent and selective inhibitors of Group VIA calcium-independent phospholipase A

Varnavas D Mouchlis, Christophe Morisseau, Bruce D Hammock, Sheng Li, J Andrew McCammon, Edward A Dennis

Abstract read
In one paragraph

Article in Bioorganic & medicinal chemistry, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

  1. Specificity mechanism of Group VIA calcium-independent phospholipase ABiochimica et biophysica acta. Molecular and cell biology of lipids · 2025
    Article
  2. Article
  3. Article
  4. Review
  5. Each phospholipase ABiochimica et biophysica acta. Molecular and cell biology of lipids · 2022
    Article
  6. Article
  7. Article
  8. Small-molecule inhibitors as potential therapeutics and as tools to understand the role of phospholipases ABiochimica et biophysica acta. Molecular and cell biology of lipids · 2019
    Review
  9. Phospholipase ABiochimica et biophysica acta. Molecular and cell biology of lipids · 2019
    Review
  10. iPLABiochimica et biophysica acta. Molecular and cell biology of lipids · 2019
    Review
  11. Article
  12. Article
  13. Article
  14. Review of four major distinct types of human phospholipase AAdvances in biological regulation · 2018
    Review
  15. Article
  16. 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

6 authors.

Varnavas D MouchlisDepartment of Pharmacology and Department of Chemistry and Biochemistry, School of Medicine, University of California, San Diego, La Jolla, CA 92093-0601, USA. Electronic address: vmouchlis@gmail.com.
Christophe MorisseauDepartment of Entomology and Nematology and UC Davis Comprehensive Cancer Research Center, University of California, Davis, CA 95616, USA.
Bruce D HammockDepartment of Entomology and Nematology and UC Davis Comprehensive Cancer Research Center, University of California, Davis, CA 95616, USA.
Sheng LiDepartment of Medicine, University of California, San Diego, La Jolla, CA 92093-0601, USA.
J Andrew McCammonDepartment of Pharmacology and Department of Chemistry and Biochemistry, School of Medicine, University of California, San Diego, La Jolla, CA 92093-0601, USA. Electronic address: jmccammon@ucsd.edu.
Edward A DennisDepartment of Pharmacology and Department of Chemistry and Biochemistry, School of Medicine, University of California, San Diego, La Jolla, CA 92093-0601, USA. Electronic address: edennis@ucsd.edu.

Funding

Workshop on Environmental Technology Transfer and EntrepreneurshipP42ES004699 · NIEHS · UNIVERSITY OF CALIFORNIA DAVIS · PI YANG, JUN · 1987 to 2021
$50.1M
National Biomedical Computation Resource - Competitive Revision SupplementP41GM103426 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI AMARO, ROMMIE E · 2012 to 2019
$14.0M
ACTION OF LIPOLYTIC ENZYMESR01GM020501 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI DENNIS, EDWARD A · 1985 to 2020
$7.3M
HYDROLYTIC ENZYMES IN THE METABOLISM OF TOXINSR01ES002710 · NIEHS · UNIVERSITY OF CALIFORNIA DAVIS · PI HAMMOCK, BRUCE D · 1985 to 2018
$4.0M
DESIGN OF AMPHIPHILIC PEPTOID ASSEMBLIESF32GM020501 · NIGMS · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI BURKOTH, TIMOTHY S · 2000 to 2002
$75k
NIEHS NIH HHS P42 ES004699NIEHS NIH HHS R01 ES002710NIGMS NIH HHS F32 GM020501NIGMS NIH HHS P41 GM103426NIGMS NIH HHS R01 GM020501
6 · The paper itself

Abstract

Potent and selective inhibitors for phospholipases A

Indexed as

Computer-Aided DesignDeuterium Exchange MeasurementDrug DesignDose-Response Relationship, DrugHumansMass SpectrometryMolecular StructurePhospholipase A2 InhibitorsPhospholipases A2Structure-Activity RelationshipPhospholipase A2 InhibitorsPhospholipases A2DockingDXMSMD simulationsPhospholipase A(2)Structure–activity relationshipThioetherTrifluoromethylketones

Identifiers

PMID27320659
PMCPMC5053890

What OpenQuestion holds

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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.