Evidence map›Paper›PMID 30209076›Full record

ArticleJournal of lipid research2018

Enzymatic synthesis and chemical inversion provide both enantiomers of bioactive epoxydocosapentaenoic acids.

Maris A Cinelli, Jun Yang, Amy Scharmen, Joey Woodman, Lalitha M Karchalla, Kin Sing Stephen Lee

Abstract read
In one paragraph

Article in Journal of lipid research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

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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.

Maris A CinelliDepartment of Pharmacology and Toxicology, Michigan State University, East Lansing, MI 48824.ORCID 0000-0002-5887-7038
Jun YangDepartment of Entomology and Nematology University of California at Davis, Davis, CA 95616.
Amy ScharmenDepartment of Pharmacology and Toxicology, Michigan State University, East Lansing, MI 48824.
Joey WoodmanDepartment of Pharmacology and Toxicology, Michigan State University, East Lansing, MI 48824.
Lalitha M KarchallaDepartment of Pharmacology and Toxicology, Michigan State University, East Lansing, MI 48824.
Kin Sing Stephen LeeDepartment of Pharmacology and Toxicology, Michigan State University, East Lansing, MI 48824 sing@msu.edu.ORCID 0000-0003-4541-3063

Funding

Workshop on Environmental Technology Transfer and EntrepreneurshipP42ES004699 · NIEHS · UNIVERSITY OF CALIFORNIA DAVIS · PI HAMMOCK, BRUCE D · 1987 to 2021
$50.1M
Identifying the receptors of environmentally sensitive epoxy-eicosanoids with AMSR00ES024806 · NIEHS · MICHIGAN STATE UNIVERSITY · PI LEE, KIN SING STEPHEN · 2017 to 2019
$727k
NIEHS NIH HHS P42 ES004699NIEHS NIH HHS R00 ES024806
6 · The paper itself

Abstract

Epoxy PUFAs are endogenous cytochrome P450 (P450) metabolites of dietary PUFAs. Although these metabolites exert numerous biological effects, attempts to study their complex biology have been hampered by difficulty in obtaining the epoxides as pure regioisomers and enantiomers. To remedy this, we synthesized 19,20- and 16,17-epoxydocosapentaenoic acids (EDPs) (the two most abundant EDPs in vivo) by epoxidation of DHA with WT and the mutant (F87V) P450 enzyme BM3 from

Indexed as

Cytochrome P-450 Enzyme SystemDocosahexaenoic AcidsEicosapentaenoic AcidFatty Acids, UnsaturatedOxidation-ReductionStereoisomerismCytochrome P-450 Enzyme SystemDocosahexaenoic AcidsEicosapentaenoic Acideicosapentaenoic acid ethyl esterFatty Acids, Unsaturatedchemoenzymatic synthesiscytochrome P450docosahexaenoic acidepoxide inversionepoxy fatty acidslipids/chemistrypolyunsaturated fatty acids

Identifiers

PMID30209076
PMCPMC6210906

What OpenQuestion holds

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Registered trials

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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.