Evidence map›Paper›PMID 41211553›Full record

ArticleFood science and biotechnology2025

Chemoenzymatic synthesis and identification of medium- and long-chain triacylglycerol congeners.

Jaehyeon Park, Juno Lee, Jihoon Kim, Pahn-Shick Chang

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Food science and biotechnology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

Jaehyeon ParkDepartment of Agricultural Biotechnology, Seoul National University, Seoul, 08826 Republic of Korea.
Juno LeeResearch Institute of Agriculture and Life Sciences, Seoul National University, Seoul, 08826 Republic of Korea.
Jihoon KimDepartment of Agricultural Biotechnology, Seoul National University, Seoul, 08826 Republic of Korea.
Pahn-Shick ChangDepartment of Agricultural Biotechnology, Seoul National University, Seoul, 08826 Republic of Korea.ORCID 0000-0001-9645-7010

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Medium- and long-chain triacylglycerols (MLCTs) offer rapid energy release and essential nutritional benefits, making them valuable in functional foods. In this study, MLCTs containing caprylic acid (C8:0; C) and linoleic acid (C18:2; L) were synthesized via a chemoenzymatic strategy combining lipase-catalyzed reactions and Steglich esterification. Four distinct MLCT congeners-CCL, CLC, LLC, and LCL-were obtained with yields of 52-67% (asymmetrical) and 71-84% (symmetrical), and purified using preparative HPLC (> 98%). The resulting compounds were structurally characterized by HPLC-ESI-MS and

Indexed as

HPLC–ESI–MSImmobilized lipaseMedium- and long-chain triacylglycerolNMR spectroscopyRegioisomerSteglich esterificationStructured lipids

Identifiers

PMID41211553
PMCPMC12589742

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.