# New Quipazine Derivatives Active Against Drug-Resistant Oncogenic Helicobacter pylori Strains with Biofilm

**Authors:** Katarzyna Grychowska, Karolina Klesiewicz, Joanna Pęgiel, Agata Kuziak, Iwona Skiba-Kurek, Vittorio Canale, Gracjana Krzysiek-Mączka, Agata Ptak-Belowska, Kamil Piska, Paulina Koczurkiewicz-Adamczyk, Paweł Krzyżek, Tomasz Brzozowski, Paweł Zajdel, Elżbieta Karczewska

PMC · DOI: 10.3390/ijms26135997 · 2025-06-22

## TL;DR

A new quipazine derivative, compound 9c, shows antibacterial and anti-biofilm activity against drug-resistant Helicobacter pylori strains and may reduce gastric cancer risk.

## Contribution

Compound 9c is a novel quipazine derivative effective against multidrug-resistant H. pylori and exhibits anti-cancer potential.

## Key findings

- Compound 9c has antibacterial activity against drug-resistant H. pylori strains with MIC values of 2–4 µg/mL.
- It prevents biofilm formation and microbial cell auto-aggregation.
- Compound 9c reduces the viability of human gastric cancer cells with an IC50 of 3.28 µg/mL.

## Abstract

Helicobacter pylori (H. pylori) is regarded as a significant risk factor for gastritis, peptic ulcer disease, and gastric cancer. However, the increasing resistance of H. pylori strains has resulted in low eradication rates and ineffective treatments. Herein, we report on identification of a new quipazine derivative—compound 9c (N-(3-chlorobenzyl)-2-(piperazin-1-yl)quinolin-4-amine), which displayed antibacterial properties (MIC range 2–4 µg/mL) against H. pylori CagA-positive reference strains associated with an increased risk of gastric cancer, including metronidazole-resistant ATCC 43504, clarithromycin-resistant ATCC 700684 and susceptible J99 strain, as well as clinical, multidrug-resistant isolate (3CML, resistant to clarithromycin, metronidazole and levofloxacin). Compound 9c showed bacteriostatic activity (MBC/MIC ratio > 4), demonstrated antibiofilm-forming properties and prevented auto-aggregation of microbial cells. It also displayed an additive effect in ½ MIC (2 µg/mL) when administered with clarithromycin and/or metronidazole. Compound 9c had no impact on gut microbiota reference strains of S. aureus, E. coli, E. faecalis and L. paracasei as well as no hemolytic activity against sheep erythrocytes. Finally, by reducing the viability of the SNU-1 human gastric cancer cell line (IC50 = 3.28 μg/mL), compound 9c might offer important implications regarding the oncogenic characteristics of cagA+ H. pylori strains.

## Linked entities

- **Chemicals:** quipazine (PubChem CID 5011), clarithromycin (PubChem CID 84029), metronidazole (PubChem CID 4173), levofloxacin (PubChem CID 149096)
- **Diseases:** gastritis (MONDO:0004966), peptic ulcer disease (MONDO:0004247), gastric cancer (MONDO:0001056)
- **Species:** Helicobacter pylori (taxon 210)

## Full-text entities

- **Genes:** CagA [NCBI Gene 48200769]
- **Diseases:** gastric cancer (MESH:D013274), gastritis (MESH:D005756), peptic ulcer disease (MESH:D010437)
- **Chemicals:** metronidazole (MESH:D008795), Quipazine (MESH:D011814), levofloxacin (MESH:D064704), clarithromycin (MESH:D017291), 9c (-)
- **Species:** Ovis aries (domestic sheep, species) [taxon 9940], Escherichia coli (E. coli, species) [taxon 562], Helicobacter pylori (species) [taxon 210], Homo sapiens (human, species) [taxon 9606], Enterococcus faecalis (species) [taxon 1351], Lacticaseibacillus paracasei (species) [taxon 1597]
- **Cell lines:** ATCC 43504 — Homo sapiens (Human), Lung adenocarcinoma, Cancer cell line (CVCL_0023), J99 — Homo sapiens (Human), Childhood T acute lymphoblastic leukemia, Cancer cell line (CVCL_U323), SNU-1 — Homo sapiens (Human), Gastric adenocarcinoma, Cancer cell line (CVCL_0099)

## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12250555/full.md

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Source: https://tomesphere.com/paper/PMC12250555