Design, Synthesis, and Antifungal Evaluation of Novel Cuminic Acid Derivatives as Potential Laccase Inhibitors DOI
Zihui Yang,

Yigui Qiu,

Daojun Jin

и другие.

Journal of Agricultural and Food Chemistry, Год журнала: 2024, Номер unknown

Опубликована: Ноя. 27, 2024

In search of novel natural product-based fungicides, 49 cuminic acid derivatives were designed, synthesized, and screened for their in vitro antifungal effects toward seven phytopathogenic fungi oomycetes. Consequently, several exhibited strong activities

Язык: Английский

Design and synthesis of bis(indolyl)-hydrazide-hydrazone derivatives and their antifungal activities against plant pathogen fungi DOI
Haowei Huang,

Jinrui Tang,

Kunrong Dang

и другие.

Natural Product Research, Год журнала: 2024, Номер unknown, С. 1 - 6

Опубликована: Июнь 28, 2024

A series of bis(indolyl)-hydrazide-hydrazone derivatives were synthesised, and their structures characterised using

Язык: Английский

Процитировано

1

Pinonic Acid Derivatives Containing Thiourea Motif: Promising Antifungal Lead Compound Targeting Cellular Barrier of Colletotrichum fructicola DOI
Jiulong Wang,

Xinying Duan,

Jing Li

и другие.

Journal of Agricultural and Food Chemistry, Год журнала: 2024, Номер unknown

Опубликована: Окт. 2, 2024

In order to explore novel antifungal lead compounds from plant essential oil, thirty-two pinonic acid derivatives containing thiourea groups were designed and synthesized using α-pinene as a raw material. One of these compound

Язык: Английский

Процитировано

1

l-Isoleucine-Derived Amide-hydrazide Compounds Evaluated as a Novel Potential Agricultural Fungicide DOI
Jing Chang,

Yufei Gong,

Wenfei Zhang

и другие.

Journal of Agricultural and Food Chemistry, Год журнала: 2024, Номер unknown

Опубликована: Ноя. 18, 2024

Building upon previous structure–activity relationships about the fungicidal amide and hydrazide lead structures, 24 novel amide-hydrazide compounds were designed synthesized with L-isoleucine as initial skeleton to explore impact of substituents in bridge on activity. Among these compounds, A5 exhibited excellent broad spectrum inhibitory activity, along satisfactory vivo protective efficiency against R. solani at concentrations 200 50 μg·mL–1. Scanning electron microscopy (SEM) transmission (TEM) observations revealed that compound induced significant morphological changes mycelium coupled vacuole rupture cytoplasmic inhomogeneity cellular structures. Transcriptomic metabolomic analyses indicated that, following treatment, differentially expressed genes metabolites significantly enriched carbohydrate metabolism-related pathways well lipid metabolism-associated pathways, including glycerophospholipid metabolism, steroid biosynthesis, arachidonic acid sphingolipid metabolism. Additionally, demonstrated low toxicity zebrafish, survival rates 100% 60% 1 10 μg·mL–1, respectively, over a period 7 days. The above results provide theoretical guidance for development green candidates.

Язык: Английский

Процитировано

1

Design, Synthesis, and Antifungal Evaluation of Novel Cuminic Acid Derivatives as Potential Laccase Inhibitors DOI
Zihui Yang,

Yigui Qiu,

Daojun Jin

и другие.

Journal of Agricultural and Food Chemistry, Год журнала: 2024, Номер unknown

Опубликована: Ноя. 27, 2024

In search of novel natural product-based fungicides, 49 cuminic acid derivatives were designed, synthesized, and screened for their in vitro antifungal effects toward seven phytopathogenic fungi oomycetes. Consequently, several exhibited strong activities

Язык: Английский

Процитировано

0