Items 31 to 40 of 157 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
3-Carboxyumbelliferyl b-D-galactopyranoside | 64664-99-9 | sc-283698 sc-283698A | 5 mg 10 mg | $124.00 $339.00 | ||
3-Carboxyumbelliferyl β-D-galactopyranoside is a fluorescent substrate notable for its specific interactions with β-galactosidase enzymes. Upon excitation below 380 nm, it exhibits a distinct fluorescence profile, enabling real-time monitoring of enzymatic activity. The carboxyumbelliferyl moiety enhances its solubility in aqueous environments, facilitating rapid substrate diffusion. Its unique structural features allow for precise kinetic studies of glycosidic bond hydrolysis, providing insights into enzyme mechanisms. | ||||||
N-alpha-CBZ-L-Arginine 7-amido-4-methylcoumarin hydrochloride | 70375-22-3 | sc-212116 | 50 mg | $329.00 | ||
N-alpha-CBZ-L-Arginine 7-amido-4-methylcoumarin hydrochloride is a fluorescent compound characterized by its unique amido and coumarin functionalities. When excited below 380 nm, it displays a strong fluorescence, making it suitable for studying molecular interactions. The presence of the carbobenzoxy group enhances its stability and solubility, while the coumarin moiety contributes to its photophysical properties. This compound's distinct reactivity as an acid halide allows for selective coupling reactions, facilitating the exploration of peptide synthesis and molecular dynamics. | ||||||
L-Alanine 7-amido-4-methylcoumarin, trifluoroacetate salt | 96594-10-4 | sc-207789 sc-207789A sc-207789B sc-207789C sc-207789D sc-207789E | 100 mg 250 mg 1 g 5 g 10 g 25 g | $63.00 $108.00 $203.00 $764.00 $1459.00 $3059.00 | ||
L-Alanine 7-amido-4-methylcoumarin, trifluoroacetate salt, exhibits remarkable fluorescence when excited below 380 nm, attributed to its unique coumarin structure. The trifluoroacetate moiety enhances solubility and stability, promoting efficient molecular interactions. Its behavior as an acid halide enables specific acylation reactions, influencing reaction kinetics and pathways in synthetic chemistry. This compound's distinct photophysical properties make it a valuable tool for probing molecular environments. | ||||||
Dihydroethidium | 104821-25-2 | sc-204724A sc-204724 | 10 mg 25 mg | $125.00 $250.00 | 42 | |
Dihydroethidium is a fluorescent compound that exhibits a striking emission profile when excited by light below 380 nm. Its unique structure allows for selective intercalation into nucleic acids, facilitating the study of reactive oxygen species in biological systems. The compound undergoes a distinct redox reaction, leading to a change in fluorescence intensity, which is sensitive to the local environment. This behavior highlights its role in elucidating cellular processes and oxidative stress dynamics. | ||||||
Proteasome Substrate II | 348086-66-8 | sc-301620 | 5 mg | $348.00 | ||
Proteasome Substrate II is a fluorescent compound that emits light when excited by wavelengths under 380 nm. Its design enables specific binding to proteasomal pathways, influencing protein degradation processes. The compound's fluorescence is modulated by conformational changes upon substrate interaction, providing insights into proteolytic activity. This dynamic behavior allows for the exploration of cellular regulation mechanisms and the intricate balance of protein turnover in various biological contexts. | ||||||
1,6-Diphenyl-1,3,5-hexatriene | 1720-32-7 | sc-213545 sc-213545A | 1 g 5 g | $79.00 $245.00 | ||
1,6-Diphenyl-1,3,5-hexatriene is a highly conjugated organic compound known for its unique photophysical properties. When excited by light below 380 nm, it exhibits strong fluorescence due to its extended π-conjugation, which enhances its light absorption and emission characteristics. The compound's rigid molecular structure facilitates efficient energy transfer, making it a valuable tool for studying molecular interactions and dynamics in various environments, including solvent effects and aggregation behavior. | ||||||
1-Methylpyrene | 2381-21-7 | sc-213366 | 100 mg | $145.00 | ||
1-Methylpyrene is a polycyclic aromatic hydrocarbon characterized by its robust π-electron system, which allows for significant light absorption and emission in the UV range. When excited below 380 nm, it undergoes rapid intersystem crossing, leading to triplet state formation. This compound exhibits notable solvent-dependent fluorescence quenching and aggregation-induced emission, revealing insights into molecular packing and environmental interactions. Its unique electronic properties make it a subject of interest in photophysical studies. | ||||||
8-Aminonaphthalene-1,3,6-trisulfonic acid disodium salt | 5398-34-5 | sc-210667 | 500 mg | $416.00 | ||
8-Aminonaphthalene-1,3,6-trisulfonic acid disodium salt features a complex sulfonic acid structure that enhances its solubility and ionic interactions in aqueous environments. Its unique electronic configuration allows for effective charge transfer processes, particularly under UV excitation below 380 nm. The compound exhibits distinct photostability and can participate in dynamic light scattering phenomena, providing insights into molecular aggregation and environmental responsiveness. | ||||||
4-Methylumbelliferyl sulfate, potassium salt | 15220-11-8 | sc-206917 sc-206917A | 500 mg 1 g | $155.00 $281.00 | ||
4-Methylumbelliferyl sulfate, potassium salt is characterized by its fluorescent properties, particularly when excited below 380 nm. The compound's unique structure facilitates strong interactions with various biomolecules, enhancing its reactivity in enzymatic assays. Its photophysical behavior includes rapid fluorescence emission and a high quantum yield, making it suitable for studying molecular dynamics. Additionally, it exhibits notable stability under light exposure, contributing to its reliability in experimental settings. | ||||||
FURA-2 pentapotassium salt | 113694-64-7 | sc-202163 | 1 mg | $148.00 | ||
FURA-2 pentapotassium salt is a fluorescent calcium indicator that exhibits distinct spectral properties when excited below 380 nm. Its unique chelation with calcium ions leads to a significant shift in fluorescence intensity, enabling precise monitoring of intracellular calcium levels. The compound's rapid kinetics allow for real-time tracking of calcium dynamics, while its high sensitivity and low background fluorescence enhance detection capabilities in complex biological systems. | ||||||