Fungal Metabolites
Items 11 to 20 of 23 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Thielavin B | 71950-67-9 | sc-202362 | 500 µg | $307.00 | ||
Thielavin B, a notable fungal metabolite, exhibits intriguing properties through its ability to disrupt cellular homeostasis. It interacts with various biomolecules, influencing enzymatic activities and metabolic flux. This compound is involved in intricate biosynthetic pathways, contributing to the production of secondary metabolites. Its amphiphilic nature enhances its solubility in diverse environments, facilitating its role in intercellular signaling and ecological interactions among fungi. | ||||||
Penigequinolone A | 180045-91-4 | sc-202277 | 500 µg | $242.00 | ||
Penigequinolone A is a fascinating fungal metabolite characterized by its unique structural features that enable specific interactions with cellular components. It plays a role in modulating metabolic pathways, particularly through its influence on enzyme regulation and substrate availability. The compound's hydrophobic characteristics allow it to integrate into lipid membranes, potentially altering membrane dynamics and fluidity. This interaction may affect cellular signaling processes, highlighting its ecological significance in fungal communities. | ||||||
UCN-02 | 121569-61-7 | sc-202377 sc-202377A sc-202377B | 500 µg 1 mg 5 mg | $220.00 $400.00 $1600.00 | 1 | |
UCN-02 is an intriguing fungal metabolite known for its distinctive ability to interact with various biomolecules, influencing cellular processes. Its unique structural configuration facilitates binding to specific receptors, potentially altering signal transduction pathways. The compound exhibits notable stability under varying environmental conditions, which may enhance its persistence in fungal ecosystems. Additionally, UCN-02's capacity to modulate gene expression underscores its role in fungal adaptation and survival strategies. | ||||||
Aspinonene | 157676-96-5 | sc-202068 sc-202068A | 1 mg 5 mg | $175.00 $693.00 | ||
Aspinonene is a fascinating fungal metabolite characterized by its complex molecular interactions that influence metabolic pathways within fungi. Its unique stereochemistry allows for selective binding to enzymes, potentially modulating their activity and affecting metabolic flux. The compound's hydrophobic nature enhances its membrane permeability, facilitating transport across cellular barriers. Furthermore, Aspinonene's role in secondary metabolite production highlights its significance in fungal ecological dynamics and competition. | ||||||
Aspergillin PZ | 483305-08-4 | sc-396535 | 1 mg | $124.00 | ||
Aspergillin PZ is a notable fungal metabolite distinguished by its intricate structural features that enable specific interactions with cellular receptors. This compound participates in unique biosynthetic pathways, influencing the synthesis of other metabolites. Its amphiphilic characteristics contribute to its ability to form micelles, impacting solubility and bioavailability. Additionally, Aspergillin PZ exhibits distinct reaction kinetics, which can alter the dynamics of metabolic processes within fungal systems. | ||||||
Moniliformin | 31876-38-7 | sc-359847 | 1 mg | $575.00 | ||
Moniliformin is a fascinating fungal metabolite characterized by its ability to disrupt cellular processes through specific molecular interactions. It is known to interfere with energy metabolism by inhibiting key enzymes, thereby affecting ATP production. This compound also exhibits unique solubility properties, allowing it to traverse biological membranes efficiently. Its presence can influence the metabolic pathways of fungi, leading to altered growth patterns and competitive dynamics within microbial communities. | ||||||
Cyclosporin A | 59865-13-3 | sc-3503 sc-3503-CW sc-3503A sc-3503B sc-3503C sc-3503D | 100 mg 100 mg 500 mg 10 g 25 g 100 g | $62.00 $90.00 $299.00 $475.00 $1015.00 $2099.00 | 69 | |
Cyclosporin A is a notable fungal metabolite recognized for its unique ability to modulate immune responses through selective binding to cyclophilins. This interaction alters protein folding and cellular signaling pathways, impacting various biological processes. Its lipophilic nature enhances membrane permeability, facilitating its distribution within cellular environments. Additionally, Cyclosporin A exhibits distinct reaction kinetics, influencing the dynamics of protein-protein interactions and cellular homeostasis. | ||||||
Wortmannin | 19545-26-7 | sc-3505 sc-3505A sc-3505B | 1 mg 5 mg 20 mg | $66.00 $219.00 $417.00 | 97 | |
Wortmannin is a potent fungal metabolite known for its selective inhibition of phosphoinositide 3-kinases (PI3Ks), crucial in various cellular signaling pathways. This compound interacts with the ATP-binding site of PI3Ks, leading to altered lipid signaling and cellular responses. Its unique structure allows for specific binding, influencing downstream effects on cell growth and survival. Wortmannin's stability and reactivity in biological systems further enhance its role in modulating cellular functions. | ||||||
4-Hydroxyalternariol | 959417-21-1 | sc-397293 sc-397293A | 1 mg 5 mg | $225.00 $793.00 | ||
4-Hydroxyalternariol is a notable fungal metabolite characterized by its ability to disrupt cellular processes through the inhibition of protein synthesis. This compound interacts with ribosomal RNA, leading to altered translation dynamics and affecting protein production. Its unique structural features facilitate specific binding to ribosomal sites, influencing the overall metabolic activity of fungi. Additionally, 4-Hydroxyalternariol exhibits distinct solubility properties, enhancing its bioavailability in various environments. | ||||||
Mevinolinic acid, monoammonium salt | 77550-67-5 | sc-221939 | 100 mg | $1980.00 | ||
Mevinolinic acid, monoammonium salt, is a distinctive fungal metabolite known for its role in modulating metabolic pathways within fungi. It exhibits unique interactions with key enzymes involved in lipid biosynthesis, effectively altering the synthesis of secondary metabolites. The compound's structural attributes enable it to form stable complexes with enzyme active sites, influencing reaction kinetics and metabolic flux. Its solubility characteristics further enhance its distribution in fungal systems, impacting overall fungal growth and development. | ||||||