# Isolation, identification, and antimicrobial effect analysis of active components from Humulus scandens against Phytophthora nicotianae

**Authors:** Xiaoyun Wu, Yuxuan Liu, Deqiang Qin, Dongmei Liu, Yongsheng Ren, Jin Tian, Siyue Lan, Xiao Ding, Xiaoping Qin

PMC · DOI: 10.3389/fpls.2026.1753587 · 2026-03-05

## TL;DR

Scientists isolated and tested compounds from Humulus scandens that effectively inhibit a plant pathogen, offering potential for eco-friendly pesticides.

## Contribution

Identification of five active compounds from Humulus scandens with strong antimicrobial effects against Phytophthora nicotianae.

## Key findings

- Five compounds were isolated from Humulus scandens with antimicrobial activity against Phytophthora nicotianae.
- Compounds 1 and 5 showed the strongest inhibitory effects with EC50 values of 51.70 and 31.71 μg/ml.
- Microscopic analysis showed that compounds 1 and 5 caused structural damage to the pathogen's mycelia.

## Abstract

Monomeric compounds from Humulus scandens that effectively inhibit Phytophthora nicotianae were isolated, and their antimicrobial effects were analyzed. Methanol extracts were isolated using a combination of activity tracking and chemical separation methods. Compound structures were identified using NMR and other techniques. Antimicrobial activity against P. nicotianae was assessed via the mycelial growth rate method with mycelial morphology further observed using optical microscopy and scanning electron microscopy. Five compounds were isolated from the ethyl acetate (EtOAc) layer of H. scandens, namely, chromone (compound 1), tectochrysin (compound 2), isorhamnetin (compound 3), hyperoside (compound 4), and Apigenin 7-glucoside (compound 5). All compounds exhibited varying degrees of antimicrobial activity. Compounds 1 and 5 demonstrated superior inhibitory effects, with EC50 values of 51.70 and 31.71 μg/ml and MIC values of 400 and 200 μg/mL, respectively. Microscopic examination revealed that compounds 1 and 5 induced distortion, deformation, shrinkage, collapse, and damage in P. nicotianae mycelia. Additionally, they increased membrane permeability and inhibited mycelial growth by disrupting cellular integrity. This study provides lead compounds for developing green botanical pesticides against tobacco black shank disease and offers data to support green agriculture initiatives.

## Linked entities

- **Chemicals:** chromone (PubChem CID 10286), tectochrysin (PubChem CID 5281954), isorhamnetin (PubChem CID 5281654), hyperoside (PubChem CID 5281643), Apigenin 7-glucoside (PubChem CID 5280704)
- **Species:** Phytophthora nicotianae (taxon 4792), Humulus scandens (taxon 228586)

## Full-text entities

- **Diseases:** black shank disease (MESH:D055008)
- **Chemicals:** chromone (MESH:D002867), isorhamnetin (MESH:C047368), Methanol (MESH:D000432), ethyl acetate (MESH:C007650), Apigenin 7-glucoside (MESH:C057792), tectochrysin (MESH:C402729), hyperoside (MESH:C021304), EtOAc (-)
- **Species:** P. nicotianae [taxon 4790], Humulus scandens (species) [taxon 228586], Nicotiana tabacum (American tobacco, species) [taxon 4097]

## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12999855/full.md

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Source: https://tomesphere.com/paper/PMC12999855