Em 570-590 nm Yellow

Doxorubicin hydrochloride exhibits notable fluorescence in the 570-590 nm range, stemming from its planar aromatic structure that enhances π-π stacking interactions. This compound demonstrates unique binding affinity to DNA, intercalating between base pairs and disrupting replication processes. Its robust photostability and distinct spectral properties make it an intriguing subject for studies on molecular interactions and cellular uptake mechanisms, revealing insights into its dynamic behavior in various environments.

ADHP is characterized by its strong fluorescence in the 570-590 nm range, attributed to its unique electronic structure that facilitates charge transfer interactions. As an acid halide, it engages in rapid acylation reactions, showcasing distinct reactivity with nucleophiles. Its ability to form stable complexes with various substrates highlights its role in catalyzing specific pathways, while its physical properties allow for effective manipulation in diverse chemical environments.

Zinpyr-1 exhibits remarkable fluorescence within the 570-590 nm spectrum, driven by its intricate molecular architecture that promotes efficient energy transfer. As an acid halide, it demonstrates swift reactivity with nucleophiles, enabling selective acylation processes. Its unique ability to form transient intermediates enhances its role in dynamic reaction pathways, while its solubility characteristics facilitate interactions in varied solvent systems, making it a versatile compound in synthetic chemistry.

Phalloidin CruzFluor™ 555 Conjugate is a highly specialized fluorescent probe that emits light in the 570-590 nm range, showcasing exceptional stability and specificity in binding to filamentous actin (F-actin). Its unique structure allows for strong non-covalent interactions, enhancing visualization in cellular studies. The conjugate's robust fluorescence intensity and photostability make it ideal for detailed imaging applications, providing clear insights into cytoskeletal dynamics.

7-Ethoxyresorufin is a fluorescent compound that exhibits emission in the 570-590 nm range, characterized by its unique ability to undergo specific molecular interactions with cytochrome P450 enzymes. This compound is notable for its rapid reaction kinetics, allowing for real-time monitoring of enzymatic activity. Its distinct electronic properties contribute to a high quantum yield, making it an effective tool for studying metabolic pathways and enzyme kinetics in various biological systems.

R-Phycoerythrin is a vibrant pigment that emits light in the 570-590 nm range, primarily due to its unique chromophore structure. This protein exhibits strong light-harvesting capabilities, facilitating energy transfer through resonance energy transfer mechanisms. Its stability under varying conditions allows for consistent fluorescence, while its interactions with other biomolecules can influence photophysical properties, enhancing its role in bioluminescent studies and environmental monitoring.

Phalloidin-tetramethylrhodamine conjugate is a fluorescent probe that emits light in the 570-590 nm range, characterized by its ability to bind specifically to F-actin filaments. This selective interaction stabilizes the actin cytoskeleton, allowing for detailed visualization of cellular structures. The conjugate's robust fluorescence intensity and photostability make it ideal for imaging applications, while its unique molecular design enhances signal clarity in complex biological environments.

Resorufin benzyl ether is a fluorescent compound that exhibits strong emission in the 570-590 nm range, attributed to its unique electron-rich structure. This compound undergoes rapid de-esterification in aqueous environments, leading to the formation of resorufin, which enhances its fluorescent properties. Its distinct photophysical behavior, including high quantum yield and sensitivity to pH changes, allows for dynamic monitoring of environmental conditions, making it a versatile tool in various analytical applications.

DAR-4M AM is a fluorescent dye characterized by its vibrant emission in the 570-590 nm range, stemming from its unique conjugated system that facilitates efficient energy transfer. This compound exhibits notable stability under various conditions, allowing for prolonged observation. Its reactivity as an acid halide enables selective interactions with nucleophiles, influencing reaction kinetics and pathways. The compound's distinct solubility properties further enhance its utility in diverse experimental setups.

Sulforhodamine B sodium salt is a fluorescent dye known for its striking emission in the 570-590 nm range, attributed to its robust conjugated structure that promotes effective light absorption and emission. This compound demonstrates exceptional photostability, making it suitable for extended imaging applications. Its ionic nature enhances solubility in aqueous environments, facilitating interactions with various biomolecules. Additionally, it exhibits unique binding affinities, influencing its behavior in complex biological systems.