Synthesis, Anti‐Fibrotic Activity, and Density Functional Theory Calculations of Novel Carboxylic Acid Analogs Containing Pyrrole and Imidazole Rings

Idiopathic pulmonary fibrosis (IPF) is a progressive and fatal interstitial lung disease with limited treatment options and poor prognosis. Current therapies, Pirfenidone and Nintedanib, slow disease progression but cannot reverse established fibrosis, underscoring the urgent need for innovative strategies. Oxidative stress and hypoxia-inducible factor-1α (HIF-1α) signaling are central to IPF pathogenesis, where the interplay between reactive oxygen species (ROS), TGF-β1, and stabilized HIF-1α forms a self-perpetuating loop that promotes fibroblast activation and extracellular matrix (ECM) deposition. To interrupt this pathological cycle, we rationally designed and synthesized four small molecules, two imidazole- and two pyrrole-based derivatives, with dual antioxidants and HIF-1α inhibitory potential. Their antioxidant potential was assessed using DPPH and DCFDA assays, while density functional theory (DFT) calculations and ADME profiling confirmed their chemical stability and drug-likeness. In vitro screening identified compound 2a as the lead candidate based on its superior ability to inhibit HIF-1α and suppress fibrotic markers, including collagen III, fibronectin, and vimentin, in TGF-β1-stimulated A549 and MRC-5 cells. In vivo, 2a significantly attenuated collagen and fibronectin accumulation in a bleomycin-induced pulmonary fibrosis model. Mechanistically, 2a inhibited phosphorylation of Smad3 and ERK, implicating modulation of both Smad and non-Smad pathways in its anti-fibrotic effects. These findings position compound 2a as a promising dual-targeted therapeutic candidate for IPF, capable of disrupting the ROS-TGF-β1-HIF-1α axis and addressing key unmet clinical needs.

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Publication Details

Journal
Chemical Biology & Drug Design
Published
2025-08-01
DOI
https://doi.org/10.1111/cbdd.70163
Citations
1
Primary Topic
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
Type
article
Field-Weighted Citation Impact
1.52

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article

Synthesis, Anti‐Fibrotic Activity, and Density Functional Theory Calculations of Novel Carboxylic Acid Analogs Containing Pyrrole and Imidazole Rings

Chulhun Park, Ashok Malla, Sang‐Soep Nahm, Yoongho Lim et al.
1 citations
Chemical Biology & Drug Design
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
1.52
article

Synthesis, Anti‐Fibrotic Activity, and Density Functional Theory Calculations of Novel Carboxylic Acid Analogs Containing Pyrrole and Imidazole Rings

Chulhun Park, Ashok Malla, Sang‐Soep Nahm, Yoongho Lim, Moonjae Cho, Jin‐Hyuk Choi, Hiruni Nilshi Indeevarie Abeysiriwardhana
article en
1 citations

Abstract

Idiopathic pulmonary fibrosis (IPF) is a progressive and fatal interstitial lung disease with limited treatment options and poor prognosis. Current therapies, Pirfenidone and Nintedanib, slow disease progression but cannot reverse established fibrosis, underscoring the urgent need for innovative strategies. Oxidative stress and hypoxia-inducible factor-1α (HIF-1α) signaling are central to IPF pathogenesis, where the interplay between reactive oxygen species (ROS), TGF-β1, and stabilized HIF-1α forms a self-perpetuating loop that promotes fibroblast activation and extracellular matrix (ECM) deposition. To interrupt this pathological cycle, we rationally designed and synthesized four small molecules, two imidazole- and two pyrrole-based derivatives, with dual antioxidants and HIF-1α inhibitory potential. Their antioxidant potential was assessed using DPPH and DCFDA assays, while density functional theory (DFT) calculations and ADME profiling confirmed their chemical stability and drug-likeness. In vitro screening identified compound 2a as the lead candidate based on its superior ability to inhibit HIF-1α and suppress fibrotic markers, including collagen III, fibronectin, and vimentin, in TGF-β1-stimulated A549 and MRC-5 cells. In vivo, 2a significantly attenuated collagen and fibronectin accumulation in a bleomycin-induced pulmonary fibrosis model. Mechanistically, 2a inhibited phosphorylation of Smad3 and ERK, implicating modulation of both Smad and non-Smad pathways in its anti-fibrotic effects. These findings position compound 2a as a promising dual-targeted therapeutic candidate for IPF, capable of disrupting the ROS-TGF-β1-HIF-1α axis and addressing key unmet clinical needs.

Chemical Biology & Drug DesignVol. 106(2)
Konkuk University (KR), Jeju TechnoPark (KR), Jeju National University (KR)
Ministry of Education, National Research Foundation, National Research Foundation of Korea, Ministry of Education, India, Ministry of SMEs and Startups
Good health and well-being
Openalex Percentile: Top 15%
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
1.52
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