Items 1 to 10 of 171 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
4-Methylumbelliferyl α-L-Idopyranosiduronic acid, Sodium Salt | 89157-94-8 | sc-216951 | 5 mg | $336.00 | ||
4-Methylumbelliferyl α-L-Idopyranosiduronic acid, Sodium Salt, showcases intriguing fluorescence properties, making it a valuable tool for studying enzymatic activities. Its unique structure allows for specific interactions with biomolecules, enhancing its role in glycosidase assays. The compound's solubility in aqueous environments facilitates its use in various biochemical contexts, while its distinct chromophoric characteristics enable sensitive detection methods, revealing insights into molecular dynamics. | ||||||
4-Methylumbelliferyl 2-Sulfamino-2-deoxy-α-D-glucopyranoside Sodium Salt | 460085-45-4 | sc-206911A sc-206911 sc-206911B sc-206911C sc-206911D | 2 mg 5 mg 10 mg 25 mg 50 mg | $224.00 $336.00 $576.00 $1224.00 $2236.00 | ||
4-Methylumbelliferyl 2-Sulfamino-2-deoxy-α-D-glucopyranoside Sodium Salt exhibits remarkable fluorescence characteristics, which are pivotal for probing enzymatic mechanisms. Its structural design promotes selective binding to glycosidases, influencing reaction kinetics and specificity. The compound's high solubility in water enhances its compatibility in diverse biochemical assays, while its unique chromophore allows for precise monitoring of molecular interactions, shedding light on dynamic biological processes. | ||||||
MeOSuc-AAPV-AMC | 72252-90-5 | sc-201163 | 5 mg | $153.00 | 19 | |
MeOSuc-AAPV-AMC is a coumarin derivative known for its distinctive photophysical properties, which facilitate real-time monitoring of enzymatic activity. Its unique structure enables efficient substrate recognition, leading to enhanced reaction rates in specific enzymatic pathways. The compound's hydrophobic characteristics contribute to its partitioning behavior in various environments, allowing for tailored interactions with biomolecules. This versatility makes it a valuable tool for studying complex biochemical systems. | ||||||
Coumarin 6 | 38215-36-0 | sc-217955 sc-217955A sc-217955B sc-217955C | 1 g 5 g 10 g 25 g | $90.00 $244.00 $362.00 $764.00 | 3 | |
Coumarin 6 is a notable coumarin derivative characterized by its strong fluorescence and unique solvatochromic behavior, which allows it to exhibit varying emission spectra in different solvents. Its molecular structure promotes specific π-π stacking interactions, enhancing its stability and reactivity in photochemical processes. Additionally, Coumarin 6's ability to form hydrogen bonds can influence its solubility and interaction with various substrates, making it an intriguing subject for studies in molecular dynamics and photophysics. | ||||||
Coumarin 153 | 53518-18-6 | sc-214766 sc-214766A sc-214766B | 100 mg 1 g 5 g | $45.00 $615.00 $2553.00 | ||
Coumarin 153 is distinguished by its exceptional photophysical properties, particularly its high quantum yield and pronounced fluorescence in the visible spectrum. This compound exhibits unique aggregation behavior, leading to distinct emission characteristics in concentrated solutions. Its molecular architecture facilitates strong dipole-dipole interactions, which can significantly affect its reactivity in photochemical reactions. Additionally, Coumarin 153's ability to engage in non-covalent interactions enhances its role in studies of energy transfer and molecular recognition. | ||||||
Ac-YVAD-AFC | 219137-85-6 | sc-311282 sc-311282A | 5 mg 10 mg | $163.00 $316.00 | 3 | |
Ac-YVAD-AFC is a synthetic peptide that exhibits unique interactions with caspases, particularly in the context of apoptosis. Its structure allows for selective binding, facilitating the study of proteolytic activity in cellular processes. The compound's fluorescence properties enable real-time monitoring of enzymatic reactions, providing insights into reaction kinetics. Additionally, Ac-YVAD-AFC's stability under various conditions makes it a reliable tool for investigating molecular pathways in biochemical research. | ||||||
Ac-VAD-AFC | sc-300156 sc-300156A | 5 mg 10 mg | $166.00 $324.00 | 1 | ||
Ac-VAD-AFC is a synthetic compound characterized by its ability to interact with specific proteases, particularly in the context of cellular signaling. Its unique structure enhances substrate specificity, allowing for precise monitoring of enzymatic activity. The compound exhibits notable fluorescence, which aids in visualizing reaction dynamics and kinetics. Furthermore, Ac-VAD-AFC's robust stability across diverse experimental conditions makes it an effective probe for dissecting complex biochemical pathways. | ||||||
Mito Red | 1021902-10-2 | sc-301164 | 8 x 50 µg | $404.00 | 5 | |
Mito Red is a coumarin derivative known for its distinctive photophysical properties, particularly its strong fluorescence and high quantum yield. This compound exhibits unique interactions with mitochondrial membranes, facilitating selective localization within cellular structures. Its reactivity profile allows for efficient energy transfer processes, making it a valuable tool for studying mitochondrial dynamics. Additionally, Mito Red's stability under varying pH conditions enhances its utility in diverse experimental setups. | ||||||
Phalloidin, Coumarin Labeled | sc-301532 | 1 mg | $262.00 | 1 | ||
Phalloidin, Coumarin Labeled is a specialized coumarin derivative characterized by its unique binding affinity to actin filaments, which allows for precise visualization of cytoskeletal structures. This compound exhibits remarkable photostability and a high degree of fluorescence, enabling detailed imaging in complex biological systems. Its distinct molecular interactions facilitate the study of cellular architecture and dynamics, providing insights into actin polymerization and cellular motility. | ||||||
Proteasome Substrate I | sc-301619 sc-301619A | 1 mg 5 mg | $38.00 $110.00 | |||
Proteasome Substrate I, a coumarin derivative, is notable for its selective interaction with proteasomal pathways, influencing protein degradation processes. This compound exhibits unique fluorescence properties, allowing for real-time monitoring of proteasome activity in cellular environments. Its structural features enable specific binding to ubiquitinated substrates, enhancing the understanding of protein turnover and cellular homeostasis. The compound's kinetic behavior reveals insights into the dynamics of proteolytic pathways. | ||||||