fusarium oxysporum

5-Heneicosylresorcinol shows inhibitory effects on the release of β-hexosaminidase from RBL-2H3 cells, it also prevents triglyceride accumulation in 3T3-L1 cells. 5-Heneicosylresorcinol has nematicidal activity against nematodes Panagrellus redivivus, Cae

3-Hydroxyacetophenone is a naturally occurring phenolic ketone exhibiting antifungal activity against Fusarium oxysporum f. sp. dianthi.

Coenzyme Q10 (CoQ10) is a naturally occurring lipid-soluble quinone compound derived from Fusarium oxysporum. Coenzyme Q10 functions as an electron carrier in the mitochondrial respiratory chain, sustaining mitochondrial energy metabolism. Coenzyme Q10 is applicable in research on mitochondrial dysfunction, oxidative stress damage, cardiovascular diseases, and neurodegenerative disorders.

DL-Pantolactone is a racemic form of pantolactone and serves as a biosynthetic precursor, an organic synthesis intermediate, and an additive in food and pharmaceuticals. DL-Pantolactone can be hydrolyzed by the lactolase of Fusarium oxysporum to form pantothenic acid. D-Pantolactone is the naturally active configuration and is an essential precursor for the biosynthesis of pantothenic acid in living organisms.

Fumonisin B1 (Fumonisin-B1) is a mycotoxin produced by Fusarium oxysporum that is widely present in crops, contaminating them and posing a significant food safety hazard.Fumonisin B1 is structurally a sphingosine and sphingomyelin analog, and inhibits the biosynthesis of complex sphingolipids through the inhibition of ceramidic synthases.

Antifungal agent 20 demonstrates significant antifungal efficacy against a range of fungal pathogens including Colletotrichum gloeosprioides, Rhizoctonia solani, Phytophthora nicotianae var. nicotianae, Diplodia pinea, Colletotrichum acutatum, and Fusarium oxysporum f. sp. niveum.

Compound 5c (Antifungal agent 64) exhibits potent fungicidal activity against Fusarium oxysporum f.sp. cucumerinum and is applicable for research in antiviral and fungicidal domains [1].

Compound 5d (Antifungal Agent 65) exhibits potent fungicidal activity against Fusarium oxysporum f.sp. cucumerinum and is utilized in antiviral and fungicidal research [1].

Compound 3i (Antifungal agent 63) is a fungicidal agent displaying potent activity against Fusarium oxysporum f.sp. cucumerinum and has applications in antiviral and fungicidal research [1].

Compound 3a (Antifungal agent 62) exhibits potent fungicidal properties, particularly against Fusarium oxysporum f.sp. cucumerinum, and is utilized in antiviral and fungicidal research [1].

32-Desmethylrapamycin, a rapamycin derivative, is an antifungal agent effective against Candida albicans, Saccharomyces cerevisiae, and Fusarium oxysporum [1].

Prolylrapamycin (21-Norrapamycin), a derivative of Rapamycin, exhibits antifungal activity. It effectively inhibits Candida albicans, Saccharomyces cerevisiae, and Fusarium oxysporum with MIC values ranging from 0.125 to 2 μg/mL.

Neoaspergillic acid (NSC 356436) (Compound 2) is a secondary metabolite produced by microorganisms. It is isolated from the endophytic fungus Aspergillus sp. SPH2 and exhibits potent antifungal activity against Alternaria alternata, Botrytis cinerea, and Fusarium oxysporum. This compound appears during the exponential growth phase of fungi and also shows antitumor and antibacterial properties.

2-(2-Heptenyl)-3-methyl-4(1H)-quinolone is a quinoline alkaloid identified in Burkholderia sp. VY81. This compound shows potential for research into bacterial diseases affecting rice (such as soft rot), as well as other plant pathogens like Pythium ultimum and Fusarium oxysporum.

Mulberrofuran H exhibits potent antifungal activity against phytopathogenic fungi Colletotrichum orbiculare, Phytophthora capsici, Corynespora cassiicola and Fusarium oxysporum.

Pisatin is an isoflavone-type plant antitoxin derived from peas (Pisum sativum) that exhibits antifungal activity. Pisatin demonstrates significant inhibitory activity against various plant pathogenic fungi, including Fusarium oxysporum, Botrytis cinerea, and Sclerotinia sclerotiorum, with IC₅₀ values ranging from 1 to 10 μM.

Thalifoline shows antifungal activity, with 100 ug against Fusarium oxysporum f. sp. lycopersici.