Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
---|---|---|---|---|---|---|
Anacardic Acid | 16611-84-0 | sc-202463 sc-202463A | 5 mg 25 mg | $100.00 $200.00 | 13 | |
Anacardic Acid acts as a potent inhibitor of tyrosinase, engaging in specific interactions that disrupt the enzyme's catalytic activity. Its unique structure allows for competitive binding at the active site, effectively blocking substrate access. The compound's ability to form hydrogen bonds and hydrophobic interactions with key amino acid residues enhances its inhibitory potency. Additionally, Anacardic Acid exhibits a favorable kinetic profile, characterized by a rapid onset of inhibition, making it a compelling candidate for modulating enzymatic reactions. | ||||||
Aloesin | 30861-27-9 | sc-202450 | 1 mg | $262.00 | 1 | |
Aloesin, derived from Aloe vera, can inhibit tyrosinase activity, thus reducing melanin production. | ||||||
L-Mimosine | 500-44-7 | sc-201536A sc-201536B sc-201536 sc-201536C | 25 mg 100 mg 500 mg 1 g | $35.00 $86.00 $216.00 $427.00 | 8 | |
L-Mimosine is a notable tyrosinase inhibitor, characterized by its ability to chelate copper ions essential for the enzyme's activity. This interaction alters the enzyme's conformation, leading to a significant reduction in its catalytic efficiency. The compound's unique side chains facilitate specific non-covalent interactions with the enzyme, enhancing its inhibitory effects. Furthermore, L-Mimosine demonstrates a distinct reaction kinetics profile, exhibiting a delayed onset of inhibition that allows for nuanced modulation of enzymatic pathways. | ||||||
5-Hydroxyindole | 1953-54-4 | sc-254834 sc-254834A | 1 g 5 g | $57.00 $130.00 | ||
5-Hydroxyindole acts as a potent tyrosinase substrate, engaging in specific interactions with the enzyme's active site. Its structural features promote effective binding, facilitating the conversion of L-tyrosine to melanin precursors. The compound exhibits unique reaction kinetics, characterized by a rapid initial phase followed by a slower steady-state, allowing for intricate regulation of melanin synthesis. Additionally, its ability to stabilize enzyme intermediates enhances the overall catalytic process. | ||||||
Arbutin | 497-76-7 | sc-221267 sc-221267A | 10 g 25 g | $118.00 $237.00 | ||
Arbutin is a naturally occurring derivative of hydroquinone and acts by inhibiting tyrosinase, thereby reducing melanin production. | ||||||
Rubrofusarin | 3567-00-8 | sc-364132 | 5 mg | $460.00 | ||
Rubrofusarin serves as a unique tyrosinase substrate, exhibiting distinct molecular interactions that enhance its binding affinity to the enzyme's active site. Its structural conformation allows for effective electron transfer during the oxidation of phenolic compounds, influencing reaction kinetics. The compound's ability to form stable enzyme-substrate complexes leads to a pronounced effect on the rate of melanin production, showcasing its role in modulating enzymatic activity through specific conformational changes. | ||||||
(R)-6-Methoxy-2,5,7,8-tetramethylchromane-2-carboxylic acid | 139658-04-1 | sc-229123 | 50 mg | $123.00 | ||
(R)-6-Methoxy-2,5,7,8-tetramethylchromane-2-carboxylic acid acts as a distinctive tyrosinase inhibitor, characterized by its ability to disrupt the enzyme's catalytic cycle. Its unique steric configuration facilitates competitive inhibition, altering substrate accessibility. The compound's hydrophobic interactions with the enzyme's active site contribute to a significant reduction in reaction velocity, highlighting its potential to modulate enzymatic pathways through structural interference. |