# Phenolic Compounds Isolated from Salix cinerea L. with Emphasis on the Pharmaceutical Relevance of Flavan-3-ols

**Authors:** Thomas Olaf Gruber, Katrin Kuck, Dejan Orčić, Jörg Heilmann, Gregor Aas, Guido Jürgenliemk

PMC · DOI: 10.3390/molecules31040702 · Molecules · 2026-02-18

## TL;DR

This study identifies new phenolic compounds in willow bark and shows how they may have medicinal benefits, especially in reducing inflammation.

## Contribution

The discovery of HCH-catechin and its anti-inflammatory effect, along with insights into seasonal changes in willow bark composition.

## Key findings

- HCH-catechin significantly reduced ICAM-1 expression in human endothelial cells.
- Seasonal variations in willow bark showed increased polymerization of proanthocyanidins during the growing season.
- Mass spectrometry identified HCH adducts in the PA fraction, suggesting a unique fragmentation pattern.

## Abstract

During this phytochemical study, 13 compounds from the bark of Salix cinerea L. were isolated and their structures elucidated. These included two salicylic alcohol derivatives, one flavonol, two phenylpropanoids, two flavan-3-ols, two dimeric procyanidins, two dimeric prodelphinidins, and a unique ester of catechin (3-O-(1-hydroxy-6-oxo-2-cyclohexen-1-carboxylic acid), HCH-catechin). Furthermore, seasonal variations in the composition of Salix cortex regarding proanthocyanidins (PA) and the degree of polymerization were examined using NMR spectroscopy, revealing an increase in polymerization throughout the growing season 2020 associated with a consistent hydroxylation pattern in the B-ring. The isolated HCH-catechin was tested in vitro for its inhibitory effect on TNF-α-induced ICAM-1 expression in human microvascular endothelial cells (HMEC-1). A 24 h treatment with a 25 µM solution of HCH-catechin significantly reduced ICAM-1 expression (83.7 ± 3.2%) compared to unsubstituted catechin (97.9 ± 4.4%). Additionally, during a mass-spectrometric screening, numerous HCH adducts within the PA fraction could be identified, allowing for the proposition of a characteristic fragmentation pattern. This study establishes a foundation for a comprehensive assessment of the phenolic, PA-rich fraction in willow bark, particularly the occurrence of HCH adducts, which may contribute to the medicinal properties of Salicis cortex. Findings on seasonal variations and mass spectrometric profiling offer new insights into the quality standards for Salicis cortex as a medicinal remedy.

## Linked entities

- **Proteins:** TNF (tumor necrosis factor), ICAM1 (intercellular adhesion molecule 1)
- **Chemicals:** proanthocyanidins (PubChem CID 107876), catechin (PubChem CID 1203)
- **Species:** Homo sapiens (taxon 9606), Salix cinerea (taxon 470278)

## Full-text entities

- **Genes:** TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, ICAM1 (intercellular adhesion molecule 1) [NCBI Gene 3383] {aka BB2, CD54, P3.58}
- **Diseases:** back pain (MESH:D001416), cytotoxicity (MESH:D064420), muscle and joint aches (MESH:D063806), pain (MESH:D010146), inflammatory (MESH:D007249), injury to (MESH:D014947), fever (MESH:D005334)
- **Chemicals:** benzoate (MESH:D001565), proanthocyanidin (MESH:C013221), sodium (MESH:D012964), potassium (MESH:D011188), ampelopsin (MESH:C106407), Silica (MESH:D012822), Sephadex (MESH:C025614), ethyl acetate (MESH:C007650), 1,3A (-), acetone (MESH:D000096), tannin (MESH:D013634), MTT (MESH:C070243), PA (MESH:D044945), amphotericin B (MESH:D000666), Salicortin (MESH:C113068), Procyanidin B3 (MESH:C479581), C-2' (MESH:C023714), CO2 (MESH:D002245), FA (MESH:D005492), C-1' (MESH:C400149), H2SO4 (MESH:C033158), DMSO (MESH:D004121), flavonoid (MESH:D005419), parthenolide (MESH:C002669), formalin (MESH:D005557), H (MESH:D006859), CD (MESH:D002104), (+)-gallocatechin (MESH:C057580), flavones (MESH:D047309), formazan (MESH:D005562), salicylic acid (MESH:D020156), formic acid (MESH:C030544), PAs (MESH:D011478), methanol (MESH:D000432), Flavan-3-ols (MESH:C404987), chalcones (MESH:D047188), flavonols (MESH:D044948), C (MESH:D002244), acetonitrile (MESH:C032159), ester (MESH:D004952), N (MESH:D009584), C-4' (MESH:C058899), EDTA (MESH:D004492), benzoic acid (MESH:D019817), ammonium (MESH:D064751), PL1 (MESH:D000077543), C-6' (MESH:C117224), anisaldehyde (MESH:C024896), (+)-catechin (MESH:D002392), d4 (MESH:C024064), Tremulacin (MESH:C095421), Catechol (MESH:C034221), vanillin (MESH:C100058), Salicin (MESH:C005696), water (MESH:D014867), (+) dihydromyricetin (MESH:C472036), Aspirin (MESH:D001241), picein (MESH:C050880), 13C (MESH:C000615229), Procyanidin B1 (MESH:C479579)
- **Species:** Salix (willows, genus) [taxon 40685], Salix cinerea (species) [taxon 470278], Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090], Mycoplasma (genus) [taxon 2093]
- **Mutations:** C-2 to C
- **Cell lines:** HMEC-1 — Homo sapiens (Human), Transformed cell line (CVCL_0307), SdIII5 — Mus musculus (Mouse), Transformed cell line (CVCL_5U93)

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12943300/full.md

## References

67 references — full list in the complete paper: https://tomesphere.com/paper/PMC12943300/full.md

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Source: https://tomesphere.com/paper/PMC12943300