Items 21 to 30 of 79 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Ac-IETD-AFC | 211990-57-7 | sc-311276 sc-311276A | 5 mg 10 mg | $275.00 $444.00 | 1 | |
Ac-IETD-AFC is a fluorogenic substrate that emits fluorescence in the 380-450 nm range, characterized by its ability to undergo specific proteolytic cleavage. This compound features a unique peptide bond that enhances its sensitivity to caspase activity, leading to a significant increase in fluorescence upon enzymatic reaction. Its structural design promotes rapid reaction kinetics, making it an effective tool for studying protease activity and cellular processes. The compound's stability under various conditions further supports its utility in biochemical assays. | ||||||
Z-DEVD-AFC | sc-296746 sc-296746A | 5 mg 50 mg | $148.00 $1331.00 | 1 | ||
Z-DEVD-AFC is a fluorogenic substrate that exhibits fluorescence in the 380-450 nm range, distinguished by its selective cleavage by caspases. The compound's unique peptide sequence facilitates specific interactions with target enzymes, resulting in a pronounced fluorescence increase upon activation. Its design allows for rapid reaction kinetics, enabling real-time monitoring of proteolytic activity. Additionally, Z-DEVD-AFC demonstrates robust stability, making it suitable for diverse experimental conditions. | ||||||
Protoporphyrin-9 | 553-12-8 | sc-200327 sc-200327A sc-200327B sc-200327C | 250 mg 500 mg 1 g 5 g | $90.00 $160.00 $205.00 $1005.00 | 11 | |
Protoporphyrin-9 is a versatile compound that exhibits strong absorption in the 380-450 nm range, facilitating unique photophysical properties. Its structure allows for effective interactions with metal ions, particularly iron, leading to the formation of stable complexes. This coordination can influence electron transfer processes and enhance light-harvesting efficiency. Additionally, Protoporphyrin-9's distinct conjugated system contributes to its remarkable stability and reactivity under various environmental conditions. | ||||||
Chlorophyll, oil soluble | 1406-65-1 | sc-337628 | 100 g | $209.00 | ||
Chlorophyll, oil soluble, is characterized by its ability to absorb light in the 380-450 nm range, which is crucial for its role in photosynthesis. Its unique hydrophobic structure allows for efficient integration into lipid membranes, enhancing its interaction with light and facilitating energy transfer. The presence of a porphyrin ring enables strong π-π stacking interactions, promoting stability and reactivity. This compound also exhibits distinct fluorescence properties, making it a key player in photochemical processes. | ||||||
Ac-VEID-AFC | sc-311280 sc-311280A | 5 mg 10 mg | $256.00 $456.00 | 1 | ||
Ac-VEID-AFC is a fluorescent substrate that exhibits strong absorption in the 380-450 nm range, making it ideal for studying proteolytic activity. Its unique peptide bond structure allows for specific interactions with proteases, leading to distinct cleavage patterns. The compound's design incorporates a fluorophore that enhances signal intensity upon enzymatic hydrolysis, facilitating real-time monitoring of reaction kinetics. Additionally, its stability under various conditions ensures reliable performance in biochemical assays. | ||||||
2-Aminoacridone | 27918-14-5 | sc-213751 sc-213751A | 25 mg 100 mg | $99.00 $267.00 | ||
2-Aminoacridone is a fluorescent compound characterized by its strong absorption in the 380-450 nm range, which enables effective detection in various analytical applications. Its unique acridine structure facilitates intercalation with nucleic acids, promoting distinct photophysical properties. The compound exhibits notable quantum yield and photostability, allowing for prolonged observation in fluorescence studies. Its reactivity with electrophiles also opens pathways for diverse chemical transformations, enhancing its utility in synthetic chemistry. | ||||||
C-6 NBD-dihydro-Ceramide | 114301-95-0 | sc-204662 sc-204662A | 1 mg 5 mg | $250.00 $1020.00 | ||
C-6 NBD-dihydro-Ceramide is a fluorescent lipid derivative that exhibits strong absorption in the 380-450 nm range, making it a valuable tool for studying membrane dynamics. Its unique structure allows for specific interactions with lipid bilayers, influencing membrane fluidity and organization. The compound's photophysical properties, including high quantum yield, enable sensitive detection in imaging applications. Additionally, its ability to participate in lipid signaling pathways highlights its role in cellular processes. | ||||||
7-(Diethylamino)coumarin-3-carbonyl azide | 157673-16-0 | sc-210585 | 25 mg | $148.00 | ||
7-(Diethylamino)coumarin-3-carbonyl azide is a vibrant fluorescent compound that absorbs light in the 380-450 nm range, showcasing remarkable photostability and a high extinction coefficient. Its azide functional group facilitates unique click chemistry reactions, enabling selective labeling and conjugation with various biomolecules. The compound's distinct electronic properties contribute to its efficient energy transfer mechanisms, making it a versatile candidate for probing molecular interactions and dynamics in complex systems. | ||||||
(2-Pyridyl)dithiobimane | 385398-64-1 | sc-216263 | 5 mg | $350.00 | ||
(2-Pyridyl)dithiobimane is a distinctive fluorescent compound that exhibits strong absorption in the 380-450 nm range. Its unique dithiobimane structure allows for effective electron transfer and interaction with thiol groups, enhancing its reactivity in redox processes. The compound's ability to form stable complexes with metal ions further influences its photophysical properties, making it an intriguing subject for studying molecular dynamics and environmental sensing. | ||||||
1-(4-Methoxyphenyl)-6-phenylhexatriene | 3893-10-5 | sc-213268 | 25 mg | $150.00 | ||
1-(4-Methoxyphenyl)-6-phenylhexatriene is a fascinating conjugated system characterized by its extended π-conjugation, which leads to significant light absorption in the 380-450 nm range. This compound exhibits unique photophysical behavior, including high fluorescence quantum yields and distinct solvatochromic effects. Its molecular structure facilitates intramolecular interactions that influence excited-state dynamics, making it a valuable model for exploring energy transfer mechanisms and photostability in organic materials. |