# Characterization of the Active Ingredients and Prediction of the Potential Anticolitis Mechanism of the Feng-Liao-Chang-Wei-Kang Capsule via Mass Spectrometry and Network Pharmacology

**Authors:** Tingting Liu, Zhijiang He, Witiao Lv, Liyun Deng, Xizhe Sun, Yanfei Chen

PMC · DOI: 10.1155/jamc/2948965 · Journal of Analytical Methods in Chemistry · 2025-05-05

## TL;DR

This study identifies active ingredients in the FLCWK capsule and predicts how they may help treat colitis through specific biological pathways.

## Contribution

The study combines mass spectrometry and network pharmacology to characterize active anticolitis ingredients in a traditional Chinese medicine capsule.

## Key findings

- 115 components were identified in the FLCWK capsule using UPLC-Q-Exactive Orbitrap MS.
- 46 compounds with good bioavailability were selected as active ingredients, including 4′,5-dihydroxyflavone and apigenin.
- Active ingredients may target 352 proteins, modulating pathways like MAPK and PI3K-Akt to reduce inflammation in colitis.

## Abstract

The Feng-Liao-Chang-Wei-Kang (FLCWK) capsule is a nationally protected Chinese patent medicine for the treatment of colitis. However, the potential active components and the pharmacological mechanism underlying the anticolitis effect of the FLCWK capsule remain unclear. This study aimed to reveal the active ingredients and possible anticolitis mechanism of the FLCWK capsule using an integrated approach combining mass spectrometry and network pharmacology analysis. Ultra-performance liquid chromatography plus Q-Exactive Orbitrap tandem mass spectrometry (UPLC-Q-Exactive Orbitrap MS) was applied to identify the components of the FLCWK capsule. A network pharmacology study, including target gene prediction and functional enrichment, was applied to screen the active ingredients of the FLCWK capsule and explore its potential mechanism for the treatment of colitis. A total of 115 components were identified in the FLCWK capsule. Network pharmacology results showed that 46 of these compounds with good bioavailability and drug-likeness, such as 4′,5-dihydroxyflavone, pinostrobin, naringenin chalcone, apigenin, and morin, were selected as active ingredients. The active ingredients may act on 352 core protein targets, including EGFR, AKT1, PIK3R1, PIK3CB, and MAPK1, thereby modulating relevant pathways, such as MAPK and PI3K-Akt signaling pathways, and thus alleviating inflammation and intestinal damage in colitis. This study provided a useful approach to identify active components and the anticolitis mechanism of the FLCWK capsule and built up a reliable foundation for its clinical treatment.

## Linked entities

- **Genes:** EGFR (epidermal growth factor receptor) [NCBI Gene 1956], AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207], PIK3R1 (phosphoinositide-3-kinase regulatory subunit 1) [NCBI Gene 5295], PIK3CB (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta) [NCBI Gene 5291], MAPK1 (mitogen-activated protein kinase 1) [NCBI Gene 5594]
- **Chemicals:** 4′,5-dihydroxyflavone (PubChem CID 165521), pinostrobin (PubChem CID 73201), naringenin chalcone (PubChem CID 5280960), apigenin (PubChem CID 5280443)
- **Diseases:** colitis (MONDO:0005292)

## Full-text entities

- **Genes:** AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207] {aka AKT, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA}, PIK3CB (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta) [NCBI Gene 5291] {aka P110BETA, PI3K, PI3KBETA, PIK3C1}, MAPK1 (mitogen-activated protein kinase 1) [NCBI Gene 5594] {aka ERK, ERK-2, ERK2, ERT1, MAPK2, NS13}, PIK3R1 (phosphoinositide-3-kinase regulatory subunit 1) [NCBI Gene 5295] {aka AGM7, GRB1, IMD36, p85, p85-ALPHA, p85alpha}, EGFR (epidermal growth factor receptor) [NCBI Gene 1956] {aka ERBB, ERBB1, ERRP, HER1, NISBD2, NNCIS}
- **Diseases:** damage (MESH:D020263), inflammation (MESH:D007249), colitis (MESH:D003092)
- **Chemicals:** morin (MESH:C008548), 4',5-dihydroxyflavone (-), pinostrobin (MESH:C411294), apigenin (MESH:D047310), naringenin chalcone (MESH:C027329)

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12069849/full.md

## References

37 references — full list in the complete paper: https://tomesphere.com/paper/PMC12069849/full.md

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Source: https://tomesphere.com/paper/PMC12069849