SEE ALSO...
Items 1 to 10 of 21 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
α-Amyloid Precursor Protein Modulator | 497259-23-1 | sc-204424 | 1 mg | $322.00 | 2 | |
α-Amyloid Precursor Protein Modulator functions as an enzyme that plays a critical role in cellular signaling pathways. It interacts specifically with metal ions, influencing its conformation and activity. This modulation affects the cleavage of amyloid precursor proteins, impacting the kinetics of enzymatic reactions. Its unique structural features allow for selective binding, which can alter downstream signaling cascades, thereby influencing cellular homeostasis and response mechanisms. | ||||||
PS 48 | 1180676-32-7 | sc-361297 sc-361297A | 10 mg 25 mg | $140.00 $443.00 | 2 | |
PS 48 acts as an enzyme that facilitates specific biochemical reactions through its unique catalytic mechanism. It exhibits a high affinity for substrate binding, which enhances its reaction kinetics. The enzyme's active site is finely tuned to stabilize transition states, promoting efficient conversion of substrates. Additionally, PS 48 demonstrates distinct allosteric regulation, allowing it to modulate its activity in response to varying concentrations of cofactors, thereby influencing metabolic pathways. | ||||||
Lactosyl Ceramide | 4682-48-8 | sc-204051 | 1 mg | $238.00 | ||
Lactosyl Ceramide functions as an enzyme by participating in glycosylation processes, where it catalyzes the transfer of sugar moieties to lipid molecules. Its structure allows for specific interactions with lipid bilayers, enhancing membrane fluidity and stability. The enzyme exhibits unique substrate specificity, favoring certain glycosidic linkages, and its kinetic properties are influenced by environmental factors, which can alter its catalytic efficiency and reaction pathways. | ||||||
Sp-Adenosine 3′,5′-cyclic monophosphorothioate triethylammonium salt | 93602-66-5 | sc-258176 | 1 mg | $143.00 | ||
Sp-Adenosine 3',5'-cyclic monophosphorothioate triethylammonium salt acts as an enzyme by modulating intracellular signaling pathways through its role as a second messenger. Its unique phosphorothioate modification enhances resistance to enzymatic degradation, allowing for prolonged activity. The compound interacts specifically with protein kinases, influencing phosphorylation events and cellular responses. Its kinetic behavior is characterized by rapid activation and a distinct affinity for target proteins, shaping various biochemical pathways. | ||||||
Lipoprotein Lipase Activator | 133208-93-2 | sc-204059 | 5 mg | $141.00 | ||
Lipoprotein Lipase Activator functions as an enzyme that enhances the hydrolysis of triglycerides in lipoproteins, facilitating lipid metabolism. It exhibits unique substrate specificity, interacting with various lipoprotein particles to promote efficient fat breakdown. The activator influences reaction kinetics by increasing the enzyme's catalytic efficiency, leading to accelerated lipid mobilization. Its role in lipid transport and energy homeostasis is critical, as it modulates the availability of fatty acids for cellular uptake. | ||||||
Guanosine-3′,5′-cyclic Monophosphate, 8-(2-Aminophenylthio)-Sodium Salt | 144509-87-5 | sc-203335 | 5 µmol | $260.00 | ||
Guanosine-3′,5′-cyclic Monophosphate, 8-(2-Aminophenylthio)-Sodium Salt acts as a potent enzyme modulator, influencing intracellular signaling pathways. It uniquely interacts with specific protein kinases, enhancing phosphorylation processes that regulate various cellular functions. This compound exhibits distinct reaction kinetics, promoting rapid signal transduction and amplifying responses to external stimuli. Its ability to stabilize enzyme conformations further optimizes catalytic activity, making it a key player in cellular communication. | ||||||
NOR-3 | 163180-49-2 | sc-202738 sc-202738A | 5 mg 10 mg | $130.00 $289.00 | ||
NOR-3 functions as a specialized enzyme that facilitates unique molecular interactions within metabolic pathways. It exhibits a distinctive affinity for substrate binding, leading to enhanced reaction rates and specificity. The compound's structural features allow for effective stabilization of transition states, optimizing catalytic efficiency. Additionally, NOR-3 influences allosteric regulation, modulating enzyme activity in response to cellular conditions, thereby fine-tuning metabolic flux. | ||||||
GSK1016790A | 942206-85-1 | sc-255193 | 10 mg | $260.00 | 6 | |
GSK1016790A functions as a specialized enzyme, exhibiting unique catalytic properties that facilitate specific biochemical reactions. Its distinct molecular architecture allows for precise interactions with substrates, leading to enhanced reaction specificity. The compound's ability to modulate enzyme activity through allosteric mechanisms contributes to its role in metabolic pathways. Additionally, its stability under varying conditions supports consistent performance in diverse biochemical environments, making it a noteworthy player in enzymatic processes. | ||||||
N6-Methyladenosine 5′-monophosphate sodium salt | 81921-35-9 | sc-215524A sc-215524B sc-215524 sc-215524D sc-215524C | 5 mg 10 mg 25 mg 100 mg 50 mg | $166.00 $249.00 $409.00 $979.00 $699.00 | 8 | |
N6-Methyladenosine 5'-monophosphate sodium salt acts as a pivotal enzyme, engaging in critical molecular interactions that drive cellular processes. Its unique structural conformation enables selective binding to target molecules, promoting efficient catalysis. The compound plays a significant role in regulating gene expression by influencing RNA modifications, thereby impacting various signaling pathways. Its kinetic properties allow for rapid turnover rates, enhancing metabolic adaptability in response to environmental changes. | ||||||
D-Glucosamine 6-sulfate | 91674-26-9 | sc-214810 | 25 mg | $140.00 | ||
D-Glucosamine 6-sulfate acts as a pivotal enzyme, characterized by its ability to engage in selective glycosylation reactions. Its unique sulfate group enhances binding affinity to specific substrates, promoting efficient catalysis. The compound's structural conformation allows for optimal transition state stabilization, influencing reaction kinetics. Furthermore, it plays a crucial role in modulating cellular signaling pathways, contributing to the regulation of various metabolic processes. | ||||||