ReviewNaunyn-Schmiedeberg's archives of pharmacology2026
Esculetin and its derivatives: recent advances in efficacy, mechanisms, and translational challenges.
Review in Naunyn-Schmiedeberg's archives of pharmacology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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.
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.
Who cites it
1 citing paper in PubMed.
- Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
10 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Esculetin (ESC, 6,7-dihydroxycoumarin), a naturally occurring polyphenolic coumarin found in numerous medicinal and dietary plants, has emerged as a multi-target bioactive scaffold demonstrating anti-inflammatory, antioxidant, and antiproliferative properties in diverse preclinical models. Recent investigations reveal that ESC modulates critical signaling pathways, including NF-κB, Nrf2/antioxidant response element (ARE), and mitochondrial apoptotic cascades, across multiple disease contexts encompassing dermatology, metabolic disorders, cardiovascular disease, neurodegeneration, hepatorenal protection, and malignant transformation. Structural modification of the coumarin ring system yields derivatives with enhanced target selectivity and improved metabolic stability in select compounds. However, ESC is substantially limited by poor aqueous solubility, rapid phase II metabolism, and an estimated low oral bioavailability (5-15%), representing a critical barrier to therapeutic translation. Notably, no phase II/III clinical trials have been completed, and human safety and efficacy data remain virtually absent. Recent innovations, including cocrystal technology, nanoparticle formulations, and rational structural optimization, demonstrate promise in preclinical contexts. This comprehensive review synthesizes pharmacological evidence across disease indications, evaluates bioavailability enhancement strategies, explicitly discusses evidence limitations, addresses safety considerations, and outlines translational research priorities essential for clinical or nutraceutical development.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.