Items 1 to 10 of 23 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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FTY720 Phosphate | 402615-91-2 | sc-205332 sc-205332A | 1 mg 5 mg | $177.00 $809.00 | 6 | |
FTY720 Phosphate is a notable fungal metabolite that exhibits unique interactions within cellular signaling pathways. Its structure facilitates specific binding to sphingosine-1-phosphate receptors, influencing cellular responses and migration. The compound's phosphonate group enhances its stability and reactivity, allowing for efficient modulation of lipid metabolism. Furthermore, its role in regulating immune responses highlights its intricate involvement in cellular communication and homeostasis. | ||||||
Ergosterol | 57-87-4 | sc-205313 sc-205313A | 5 g 10 g | $128.00 $209.00 | ||
Ergosterol is a key fungal metabolite that plays a crucial role in maintaining cell membrane integrity and fluidity. Its unique sterol structure allows for specific interactions with membrane proteins, influencing permeability and signaling pathways. Ergosterol is involved in the biosynthesis of other vital compounds, acting as a precursor in the synthesis of steroid-like molecules. Additionally, its presence can modulate the activity of membrane-bound enzymes, impacting various metabolic processes within fungal cells. | ||||||
beta-Sitosterol acetate | 915-05-9 | sc-291985 sc-291985A | 1 g 5 g | $148.00 $413.00 | 1 | |
Beta-Sitosterol acetate, a notable fungal metabolite, exhibits unique interactions within cellular membranes, enhancing structural stability and fluidity. Its acetate group facilitates specific hydrogen bonding and hydrophobic interactions, influencing membrane dynamics. This compound is involved in lipid metabolism pathways, potentially affecting the synthesis of other sterols and fatty acids. Furthermore, beta-Sitosterol acetate can modulate the activity of membrane-associated proteins, thereby impacting cellular signaling and metabolic regulation in fungi. | ||||||
2-Methylisoborneol solution | 2371-42-8 | sc-251786 | 1 ml | $320.00 | ||
2-Methylisoborneol solution, a distinctive fungal metabolite, is characterized by its strong hydrophobic nature, which allows it to interact effectively with lipid bilayers. This compound can influence the permeability of membranes, potentially altering the transport of ions and small molecules. Its unique structure enables specific binding to receptors, impacting signaling pathways. Additionally, 2-Methylisoborneol may play a role in the regulation of secondary metabolite production, showcasing its importance in fungal ecology. | ||||||
Triticonazole | 131983-72-7 | sc-204929 sc-204929A | 5 g 10 g | $138.00 $199.00 | ||
Triticonazole, a notable fungal metabolite, exhibits unique interactions with fungal cell membranes, disrupting ergosterol biosynthesis. This compound's specific affinity for cytochrome P450 enzymes alters metabolic pathways, leading to the inhibition of fungal growth. Its lipophilic characteristics enhance its penetration into fungal cells, facilitating rapid action. Triticonazole's distinct reaction kinetics contribute to its effectiveness in modulating fungal resistance mechanisms, highlighting its role in fungal biology. | ||||||
Aflatoxicol | 29611-03-8 | sc-391389 | 1 mg | $1200.00 | ||
Aflatoxicol, a significant fungal metabolite, is characterized by its ability to bind to cellular macromolecules, particularly nucleic acids, leading to mutagenic effects. This compound undergoes metabolic activation, resulting in reactive intermediates that can form adducts with proteins and DNA, disrupting normal cellular functions. Its hydrophobic nature allows for efficient membrane permeability, influencing its bioavailability and interaction with various biological systems. Aflatoxicol's unique pathways of biotransformation further underscore its complex role in fungal ecology. | ||||||
Citromycetin | 478-60-4 | sc-202104 | 1 mg | $373.00 | ||
Citromycetin, a notable fungal metabolite, exhibits unique interactions with cellular components, particularly through its capacity to inhibit specific enzymatic pathways. This compound is known for its role in modulating metabolic processes within fungi, influencing secondary metabolite production. Its structural features facilitate strong binding to target enzymes, altering reaction kinetics and leading to significant shifts in metabolic flux. Additionally, Citromycetin's solubility characteristics enhance its distribution within fungal cells, impacting ecological dynamics. | ||||||
Asterric acid | 577-64-0 | sc-202474 | 1 mg | $192.00 | ||
Asterric acid, a distinctive fungal metabolite, showcases remarkable interactions with cellular membranes, influencing permeability and transport mechanisms. Its unique structural configuration allows for selective binding to membrane proteins, which can modulate signal transduction pathways. This compound also participates in complex biosynthetic routes, affecting the synthesis of other metabolites. Furthermore, Asterric acid's hydrophobic properties contribute to its role in cellular compartmentalization, impacting fungal growth and adaptation. | ||||||
Terphenyllin | 52452-60-5 | sc-202358 | 1 mg | $205.00 | ||
Terphenyllin, a notable fungal metabolite, exhibits intriguing interactions with enzymatic systems, particularly influencing the activity of key metabolic enzymes. Its unique polycyclic structure facilitates specific binding to active sites, altering reaction kinetics and substrate availability. Additionally, Terphenyllin is involved in intricate biosynthetic pathways, contributing to the regulation of secondary metabolite production. Its amphiphilic nature enhances its role in membrane dynamics, affecting cellular signaling and adaptation processes. | ||||||
Thielavin A | 71950-66-8 | sc-202361 | 500 µg | $790.00 | 1 | |
Thielavin A, a distinctive fungal metabolite, showcases remarkable interactions with cellular components, particularly in modulating signal transduction pathways. Its unique structural features enable it to engage with specific receptors, influencing gene expression and metabolic regulation. Thielavin A also participates in complex biosynthetic networks, playing a crucial role in the synthesis of other metabolites. Its hydrophobic characteristics contribute to membrane fluidity, impacting cellular communication and environmental responses. |