Evidence map›Paper›PMID 33255197›Full record

ReviewMolecules (Basel, Switzerland)2020

Small Molecule Soluble Epoxide Hydrolase Inhibitors in Multitarget and Combination Therapies for Inflammation and Cancer.

Amarjyoti Das Mahapatra, Rinku Choubey, Bhaskar Datta

Open access · goldAbstract readReview
In one paragraph

Review in Molecules (Basel, Switzerland), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

26 citing papers in PubMed, 50 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Essential Oils ofFoods (Basel, Switzerland) · 2024
    Article
  13. Article
  14. Article
  15. Enhancing cancer immunotherapy via inhibition of soluble epoxide hydrolase.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  16. Article
  17. How Robust Is the Ligand Binding Transition State?Journal of the American Chemical Society · 2023
    Article
  18. Inhibitory Activity of NaturalPlants (Basel, Switzerland) · 2023
    Article
  19. Article
  20. 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

3 authors at 1 institution in 1 country.

Amarjyoti Das MahapatraDepartment of Chemistry, Indian Institute of Technology Gandhinagar, Palaj, Gandhinagar 382355, India.ORCID 0000-0002-4411-6844
Rinku ChoubeyDepartment of Chemistry, Indian Institute of Technology Gandhinagar, Palaj, Gandhinagar 382355, India.
Bhaskar DattaDepartment of Chemistry, Indian Institute of Technology Gandhinagar, Palaj, Gandhinagar 382355, India.
Indian Institute of Technology Gandhinagar · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The enzyme soluble epoxide hydrolase (sEH) plays a central role in metabolism of bioactive lipid signaling molecules. The substrate-specific hydrolase activity of sEH converts epoxyeicosatrienoic acids (EETs) to less bioactive dihydroxyeicosatrienoic acids. EETs exhibit anti-inflammatory, analgesic, antihypertensive, cardio-protective and organ-protective properties. Accordingly, sEH inhibition is a promising therapeutic strategy for addressing a variety of diseases. In this review, we describe small molecule architectures that have been commonly deployed as sEH inhibitors with respect to angiogenesis, inflammation and cancer. We juxtapose commonly used synthetic scaffolds and natural products within the paradigm of a multitarget approach for addressing inflammation and inflammation induced carcinogenesis. Structural insights from the inhibitor complexes and novel strategies for development of sEH-based multitarget inhibitors are also presented. While sEH inhibition is likely to suppress inflammation-induced carcinogenesis, it can also lead to enhanced angiogenesis via increased EET concentrations. In this regard, sEH inhibitors in combination chemotherapy are described. Urea and amide-based architectures feature prominently across multitarget inhibition and combination chemotherapy applications of sEH inhibitors.

Indexed as

AnimalsAnti-Inflammatory AgentsAntineoplastic AgentsAntineoplastic Combined Chemotherapy ProtocolsBiomarkersCatalysisCell Transformation, NeoplasticDrug Therapy, CombinationEnzyme InhibitorsEpoxide HydrolasesHumansInflammationMolecular Targeted TherapyNeoplasmsNeovascularization, PathologicSolubilityAnti-Inflammatory AgentsAntineoplastic AgentsBiomarkersEnzyme InhibitorsEpoxide Hydrolasescombination chemotherapyinflammationmultitarget therapysoluble epoxide hydrolase (sEH) inhibitorsurea derivatives

Identifiers

PMID33255197
PMCPMC7727688
OpenAlexW3106851243

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.