Resorufins
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
7-Ethoxyresorufin | 5725-91-7 | sc-200606 sc-200606A | 2 mg 10 mg | $135.00 $265.00 | 6 | |
7-Ethoxyresorufin, a resorufin derivative, showcases distinctive photophysical properties, particularly in its fluorescence emission, which is influenced by its ethoxy substituent. This modification enhances its solubility and alters its interaction dynamics with biological membranes. The compound participates in specific enzymatic pathways, acting as a substrate for cytochrome P450 enzymes, which can lead to varied metabolic outcomes. Its unique structural features facilitate selective binding and reactivity, making it a significant compound in biochemical research. | ||||||
Resorufin | 635-78-9 | sc-206039 sc-206039B | 1 g 5 g | $252.00 $807.00 | 2 | |
Resorufin is a highly fluorescent compound known for its unique redox properties, which enable it to participate in electron transfer reactions. Its structure allows for strong interactions with various biomolecules, influencing reaction kinetics and pathways. The compound exhibits notable stability under physiological conditions, making it an effective probe for studying oxidative stress and cellular processes. Its distinct spectral characteristics further enhance its utility in analytical applications, providing insights into molecular interactions. | ||||||
Resorufin benzyl ether | 87687-02-3 | sc-208301 sc-208301A | 5 mg 10 mg | $98.00 $166.00 | 1 | |
Resorufin benzyl ether is a derivative that showcases enhanced lipophilicity, facilitating its penetration through biological membranes. This compound exhibits unique photophysical properties, including a pronounced fluorescence quantum yield, which is sensitive to its microenvironment. Its ether linkage influences solubility and reactivity, allowing for selective interactions with specific targets. Additionally, the compound's stability under varying pH conditions contributes to its versatility in diverse chemical environments, making it a valuable tool for probing molecular dynamics. | ||||||
Resorufin β-D-galactopyranoside | 95079-19-9 | sc-222246 sc-222246B sc-222246C sc-222246A | 10 mg 25 mg 50 mg 100 mg | $120.00 $240.00 $500.00 $750.00 | 5 | |
Resorufin β-D-galactopyranoside is a glycoside that exhibits remarkable specificity in enzymatic hydrolysis, primarily by β-galactosidases. This compound's structure allows for distinct molecular interactions, leading to a significant fluorescence response upon cleavage. Its unique carbohydrate moiety enhances solubility in aqueous environments, while the resorufin moiety provides a sensitive readout for monitoring enzymatic activity. The compound's kinetic behavior is influenced by substrate concentration and enzyme affinity, making it a useful model for studying glycosidase mechanisms. | ||||||
Resorufin pentyl ether | 87687-03-4 | sc-208304 sc-208304A | 1 mg 5 mg | $200.00 $620.00 | 2 | |
Resorufin pentyl ether is a lipophilic derivative that showcases unique photophysical properties, particularly in its fluorescence characteristics. The pentyl ether group enhances membrane permeability, facilitating interactions with lipid bilayers. This compound undergoes rapid de-esterification, leading to the release of resorufin, which exhibits a pronounced fluorescence increase. Its reaction kinetics are influenced by solvent polarity and temperature, making it an intriguing subject for studies on molecular dynamics and environmental behavior. | ||||||
Resorufin methyl ether | 5725-89-3 | sc-208303 sc-208303A | 1 mg 5 mg | $61.00 $209.00 | 1 | |
Resorufin methyl ether is a hydrophobic compound that exhibits remarkable fluorescence properties, making it a subject of interest in various chemical studies. The methyl ether moiety enhances its solubility in organic solvents, promoting interactions with hydrophobic environments. This compound undergoes selective hydrolysis, resulting in the formation of resorufin, which is characterized by a significant increase in fluorescence intensity. Its reactivity is influenced by pH and ionic strength, providing insights into its behavior in diverse chemical contexts. | ||||||
Resorufin sodium salt | 34994-50-8 | sc-206019 sc-206019A sc-206019B | 500 mg 1 g 5 g | $245.00 $367.00 $1403.00 | 5 | |
Resorufin sodium salt is a highly soluble, anionic dye known for its intense fluorescence, which arises from its unique conjugated structure. This compound participates in electron transfer reactions, making it a valuable probe for studying redox processes. Its interactions with metal ions can lead to quenching or enhancement of fluorescence, depending on the environment. Additionally, the salt form facilitates its stability in aqueous solutions, allowing for diverse applications in biochemical assays. | ||||||
ADHP | 119171-73-2 | sc-291898 | 25 mg | $497.00 | 1 | |
ADHP, a derivative of resorufin, exhibits unique electron transfer properties due to its conjugated system, facilitating rapid redox reactions. Its structure allows for efficient resonance stabilization, enhancing its fluorescence characteristics. The compound's ability to form stable complexes with metal ions can influence reaction kinetics, while its hydrophilic nature promotes interactions with various biomolecules. These features make ADHP a key player in studies of electron transport and energy transfer mechanisms. | ||||||