Alkaline Phosphatase Substrates
SEE ALSO...
Items 1 to 10 of 11 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Naphthol AS phosphate disodium salt | 69815-54-9 | sc-206043 sc-206043A sc-206043B | 500 mg 1 g 5 g | $159.00 $225.00 $762.00 | 1 | |
Naphthol AS phosphate disodium salt serves as a substrate for alkaline phosphatase, undergoing hydrolysis to release naphthol, which can be detected spectrophotometrically. Its unique structure facilitates specific interactions with the enzyme, promoting efficient catalysis. The compound's solubility in alkaline conditions enhances its reactivity, while its kinetic properties indicate a rapid conversion rate, making it a valuable tool for studying enzyme kinetics and activity. | ||||||
Naphthol AS-TR phosphate disodium salt | 4264-93-1 | sc-253179 sc-253179A sc-253179B | 100 mg 1 g 5 g | $72.00 $196.00 $646.00 | ||
Naphthol AS-TR phosphate disodium salt acts as a potent substrate for alkaline phosphatase, engaging in specific molecular interactions that enhance enzymatic activity. Its unique aromatic structure allows for effective binding, leading to a swift hydrolytic reaction that liberates naphthol. The compound's high solubility in alkaline environments not only boosts its reactivity but also supports diverse experimental conditions, making it an essential component in enzymatic studies and kinetic analyses. | ||||||
6-Chloro-3-indoxyl phosphate, p-toluidine salt | 159954-33-3 | sc-239096 sc-239096A | 50 mg 100 mg | $58.00 $105.00 | ||
6-Chloro-3-indoxyl phosphate, p-toluidine salt serves as a selective substrate for alkaline phosphatase, exhibiting unique reactivity due to its indole moiety. The compound undergoes rapid dephosphorylation, resulting in the formation of a colored product that facilitates real-time monitoring of enzymatic activity. Its stability in various pH conditions and ability to participate in electron transfer reactions enhance its utility in biochemical assays, providing insights into enzyme kinetics and mechanisms. | ||||||
3-Indoxyl phosphate, bis(2-amino-2-methyl-1,3-propanediol) salt | 107475-12-7 | sc-281358 sc-281358A | 100 mg 250 mg | $142.00 $250.00 | ||
3-Indoxyl phosphate, bis(2-amino-2-methyl-1,3-propanediol) salt acts as a substrate for alkaline phosphatase, characterized by its distinctive phosphate group that promotes specific enzymatic interactions. The compound exhibits a notable affinity for the enzyme, leading to efficient hydrolysis and the release of indoxyl, which can further participate in oxidation reactions. Its solubility and stability across a range of conditions make it an effective tool for studying enzyme dynamics and reaction pathways. | ||||||
3-Indoxyl phosphate, disodium salt | 3318-43-2 | sc-206651 sc-206651A | 250 mg 1 g | $214.00 $615.00 | ||
3-Indoxyl phosphate, disodium salt serves as a substrate for alkaline phosphatase, featuring a unique indole structure that enhances its interaction with the enzyme's active site. This compound undergoes rapid dephosphorylation, resulting in the generation of indoxyl, which can engage in subsequent biochemical transformations. Its high solubility and stability under various pH conditions facilitate detailed investigations into enzyme kinetics and metabolic pathways, providing insights into phosphatase activity. | ||||||
3-Indoxyl phosphate p-toluidine salt | 31699-61-3 | sc-281357 sc-281357A | 250 mg 500 mg | $162.00 $255.00 | ||
3-Indoxyl phosphate p-toluidine salt acts as a substrate for alkaline phosphatase, characterized by its distinctive p-toluidine moiety that influences enzyme affinity and specificity. The compound exhibits a notable rate of hydrolysis, leading to the release of indoxyl, which can participate in further biochemical reactions. Its solubility in aqueous environments and resistance to degradation under diverse conditions make it an effective tool for studying enzymatic mechanisms and reaction dynamics. | ||||||
Naphthol AS-BI-phosphate disodium salt | 530-79-0 | sc-219334 sc-219334A | 100 mg 500 mg | $65.00 $110.00 | ||
Naphthol AS-BI-phosphate, disodium salt serves as a substrate for alkaline phosphatase, featuring a unique naphthol structure that enhances its interaction with the enzyme. This compound undergoes rapid dephosphorylation, resulting in the release of naphthol, which can engage in subsequent reactions. Its high solubility in water and stability across various pH levels facilitate detailed investigations into enzyme kinetics and the underlying mechanisms of phosphatase activity. | ||||||
Phenolphthalein monophosphate, bis(cyclohexylammonium) salt | 14815-59-9 | sc-208163 sc-208163A | 1 g 5 g | $225.00 $664.00 | ||
Phenolphthalein monophosphate, bis(cyclohexylammonium) salt acts as a substrate for alkaline phosphatase, characterized by its distinctive phenolphthalein moiety that promotes specific enzyme binding. The compound exhibits a notable rate of hydrolysis, leading to the generation of phenolphthalein, which can participate in further chemical transformations. Its amphiphilic nature enhances solubility in diverse environments, making it suitable for studying enzyme-substrate interactions and reaction dynamics. | ||||||
Naphthol AS-BI-phosphate | 1919-91-1 | sc-222042 sc-222042A | 100 mg 1 g | $96.00 $282.00 | 1 | |
Naphthol AS-BI-phosphate serves as a substrate for alkaline phosphatase, distinguished by its naphthol structure that facilitates selective enzyme recognition. The compound undergoes rapid dephosphorylation, resulting in the release of naphthol, which can engage in subsequent reactions. Its unique electronic properties and hydrophobic characteristics influence reaction kinetics, allowing for enhanced interaction with the enzyme's active site and providing insights into enzymatic mechanisms. | ||||||
p-Nitrophenyl Phosphate 50X solution | sc-358718 | 10 ml | $316.00 | |||
p-Nitrophenyl Phosphate 50X solution acts as a substrate for alkaline phosphatase, characterized by its nitrophenyl group that enhances enzyme affinity. Upon enzymatic hydrolysis, it releases p-nitrophenol, which exhibits a distinct color change, facilitating real-time monitoring of enzymatic activity. The compound's electronic structure and steric properties influence its reactivity, promoting efficient substrate turnover and providing valuable insights into enzyme kinetics and specificity. | ||||||