mycotoxin

Brevianamide F (Cyclo(L-Pro-L-Trp)), also known as cyclo-(L-Trp-L-Pro), is a naturally occurring 2,5-diketopiperazine with notable breast cancer resistance protein inhibitory activity.

Zearalenone (F2 toxin) is a mycotoxin produced mainly by fungi belonging to the genus Fusarium in foods and feeds. Possess oestrogenic activity in cattle, pigs and sheep, with low acute toxicity. Causes precocious development of mammae and other estrogenic effects in young gilts.

Deoxynivalenol (Vomitoxin) is an orally active mycotoxin belonging to the trichothecenes family, which traverses the intestinal mucosa via the paracellular pathway without being affected by P-gp/MRP, used for research on gastrointestinal inflammation such as diarrhea and vomiting.

Fusarochromanone (FC-101) is a mycotoxin produced by Fusarium marcescens with potent antiangiogenic, anticancer and antimalarial activities. Fusarochromanone induces cell death in COS7 and HEK293 cells through activation of the JNK pathway.

Citrinin is a mycotoxin that causes contamination in the food and is associated with different toxic effects. Citrinin also possesses a broad spectrum of bioactivities, including antifungal, antibacterial, and potential anticancer and neuroprotective effe

Paxilline is an indole alkaloid mycotoxin from *Penicillium paxilli*, acting as a potent BK channel inhibitor via an almost exclusively closed-channel block mechanism. Paxilline possesses significant anticonvulsant activity.

Phomopsin A, a cyclic hexapeptide mycotoxin, is isolated from the fungus Phomopsis leptostomiformis.

Ochratoxin B is produced by a variety of Aspergillus and Penicillium species and is an analog of the mycotoxin Ochratoxin A, which can contaminate agricultural products.

Zearalenone is a nonsteroidal estrogenic mycotoxin produced by Fusarium species that colonizes various grains.

3-Acetyldeoxynivalenol is a mycotoxin discovered in F. graminearum that can penetrate the blood-brain barrier and induce necrosis in mouse duodenal and spleen cells.

Aflatoxin (Aflatoxin R0) is a mutagenic and carcinogenic mycotoxin that is derived from aflatoxin B1 through metabolic processes facilitated by Rhizopus spp.

Aflatoxin G2 is a major naturally occurring mycotoxin produced by the fungi [Aspergillus flavus] and [Aspergillus parasiticus].

Aflatoxin M2 is a major metabolite of Aflatoxin B1 and is a mycotoxin produced by the fungi Aspergillus flavus and Aspergillus parasiticus.

Altertoxin I (Dihydroalterperylenol) is a quinone-type mycotoxin produced by the fungi Alternaria alternata. It exhibits mutagenic and cytotoxic properties and can mildly disrupt metabolic communication.

β-Zearalenol is a non-steroidal estrogenic mycotoxin synthesized by Fusarium species that may influence transcriptional processes and alter gene expression at the translational level. β-Zearalenol is relevant for investigations involving mycotoxin-associated endocrine signaling, reproductive toxicology, epigenetic regulation, and fungal metabolite-induced cellular responses.

Curvularin ((S)-Curvularin) is a quorum-sensing antagonist of Pseudomonas aeruginosa RhlR extractable from Curvularia lunata, a mycotoxin with anti-inflammatory activity, inhibition of cytokine-induced NO synthase, and inhibition of lipopolysaccharide-induced inflammation in antimyelocytes. study inflammation.

Enniatin A, a Fusarium mycotoxin, inhibits acyl-CoA: cholesterol acyltransferase (ACAT) with an IC50 of 22 μM in rat liver microsome enzyme assays.

Enniatins B decreases the activation of ERK (p44/p42). Enniatin B is a Fusarium mycotoxin. Enniatin B inhibits acyl-CoA: cholesterol acyltransferase (ACAT) activity with an IC50 of 113 μM in an enzyme assay using rat liver microsomes.

Enniatin B1, a Fusarium mycotoxin, crosses the blood-brain barrier, decreases the activation of ERK (p44/p42), and inhibits moderately TNF-α-induced NF-κB activation. Furthermore, it inhibits acyl-CoA: cholesterol acyltransferase (ACAT) activity, exhibiting an IC50 of 73 μM in rat liver microsome enzyme assays.

Hydrolyzed Fumonisin B1 is the backbone and the main hydrolysis product of the mycotoxin fumonisin B1 (FB1), can weakly inhibit ceramide synthase.

Moniliformin sodium salt is water-soluble mycotoxin isolate from Fusarium moniliforme.

Penicillic acid, a polyketide mycotoxin, synthesized by various species of Aspergillus and Penicillium, acts as an inhibitor of Fas ligand-induced apoptosis by impeding self-processing of caspase-8. Additionally, in vitro studies have shown that Penicillic acid displays cytotoxic properties in rat alveolar macrophages.

Alternariol is a natural product extracted from Etoac that demonstrates anti-inflammatory activity in vitro and in vivo in murine hepatoma cells and in human serum, with additional effects on toll-like receptor signaling and regulation of pro-apoptotic protein expression. Alternariol has been shown to be inactive against methyl transferase enzymes, a feature relevant to its metabolic inactivation profile.

Beauvericin, a Fusarium mycotoxin, inhibits acyl-CoA:cholesterol acyltransferase (ACAT) in rat liver microsomal enzyme assays with an IC50 value of 3 μM.