Evidence map›Paper›PMID 42103229›Full record

ArticleThe Journal of biological chemistry2026

A comprehensive discovery platform for ELOVL1 small-molecule inhibitors targeting very long-chain fatty acid synthesis in adrenoleukodystrophy.

Stephanie Holley, Gary Asmussen, Becky Lam, Zhonglin Zhao, Brian Freed, Lilu Guo, Zuzana Dostalova, Buyun Tang, Michael Kothe, Paul Lang and 6 more

Abstract read
In one paragraph

Article in The Journal of biological chemistry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

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

16 authors.

Stephanie HolleyResearch and Development, Sanofi, Cambridge, Massachusetts, USA. Electronic address: Stephanie.Holley@sanofi.com.
Gary AsmussenResearch and Development, Sanofi, Cambridge, Massachusetts, USA.
Becky LamResearch and Development, Sanofi, Cambridge, Massachusetts, USA.
Zhonglin ZhaoResearch and Development, Sanofi, Cambridge, Massachusetts, USA.
Brian FreedResearch and Development, Sanofi, Cambridge, Massachusetts, USA.
Lilu GuoResearch and Development, Sanofi, Cambridge, Massachusetts, USA.
Zuzana DostalovaResearch and Development, Sanofi, Cambridge, Massachusetts, USA.
Buyun TangResearch and Development, Sanofi, Cambridge, Massachusetts, USA.
Michael KotheResearch and Development, Sanofi, Cambridge, Massachusetts, USA.
Paul LangResearch and Development, Sanofi, Cambridge, Massachusetts, USA.
Donghui WangResearch and Development, Sanofi, Cambridge, Massachusetts, USA.
Martin HanusResearch and Development, Sanofi, Cambridge, Massachusetts, USA.
Alexei BelenkyResearch and Development, Sanofi, Cambridge, Massachusetts, USA.
Mandy CromwellResearch and Development, Sanofi, Cambridge, Massachusetts, USA.
Alla KlossResearch and Development, Sanofi, Cambridge, Massachusetts, USA.
Tatiana GladyshevaResearch and Development, Sanofi, Cambridge, Massachusetts, USA. Electronic address: Tatiana.Gladysheva@sanofi.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Adrenoleukodystrophy (ALD or X-ALD) is a rare devastating neurological disease caused by mutations in the ATP binding cassette D1 (ABCD1) gene, the product of which is involved in the transport of very long-chain fatty acids (VLCFAs) into peroxisomes for degradation by β-oxidation. Deficiency in ABCD1 results in VLCFAs accumulation in many tissues, including the brain and spinal cord. Elevated VLCFA levels, specifically C26:0, are consistent biochemical markers of ALD and are implicated in the ALD pathogenesis. ALD disease is manifested by multiple phenotypes: the most severe cerebral disease (cerebral ALD, cALD), adrenomyeloneuropathy (AMN) and adrenal insufficiency (Addison disease). VLCFA accumulation is a hallmark of all ALD phenotypes, and reduction/normalization of VLCFA levels is an attractive approach for the treatment of all ALD manifestations. VLCFAs synthesis involves enzymes from elongase of very long-chain fatty acids (ELOVL) enzyme family with ELOVL1 being a rate-limiting enzyme in C26:0 synthesis, making ELOVL1 an attractive target for medical intervention in ALD via Substrate Reduction Therapy (SRT). In this paper, we describe the in vitro assays established to support medicinal chemistry efforts to develop small-molecule ELOVL1 inhibitors for ALD. Notably, we developed novel, breakthrough in vitro methods to monitor enzymatic and cellular ELOVL1 activity, enabling high-throughput screening (HTS) of Sanofi library collections. We successfully identified CNS-active, small-molecule ELOVL1 inhibitors shown to be efficacious in the reduction of C26:0 VLCFA levels in cells and multiple tissues, including brain and spinal cord, in animal models.

Indexed as

AdrenoleukodystrophyEnzyme InhibitorsFatty Acid ElongasesFatty AcidsSmall Molecule LibrariesCells, CulturedCell SeparationChildDrug DiscoveryHumansLipid MetabolismLipidomicsMaleMicrosomesSubstrate SpecificityELOVL1 protein, humanEnzyme InhibitorsFatty Acid ElongasesFatty AcidsSmall Molecule LibrariesABCD1AMNCCALDELOVL1Fatty AcidsHTSsmall molecule inhibitorX-ALD

Identifiers

PMID42103229
PMCPMC13254579

What Socratic holds

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LicenceCC BY-NC-ND
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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 Socratic graph.