Adenylyl Cyclase Inhibitors
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Dermatan Sulfate | 54328-33-5 | sc-203916 sc-203916A | 25 mg 250 mg | $1155.00 $3131.00 | ||
Dermatan Sulfate functions as an adenylyl cyclase by modulating intracellular signaling pathways through its unique glycosaminoglycan structure. Its sulfate groups engage in specific ionic interactions, promoting the activation of G-proteins and influencing cyclic AMP production. The compound's ability to form dynamic complexes with proteins enhances its role in signal transduction, while its structural flexibility allows for diverse molecular interactions, impacting cellular responses and regulatory mechanisms. | ||||||
BPIPP | 325746-94-9 | sc-203852 sc-203852A | 10 mg 50 mg | $189.00 $797.00 | 1 | |
BPIPP acts as an adenylyl cyclase by facilitating the conversion of ATP to cyclic AMP, a crucial second messenger in cellular signaling. Its unique structural features enable specific binding to regulatory proteins, enhancing the enzyme's catalytic efficiency. The compound's hydrophobic regions promote membrane interactions, influencing its localization and activity within lipid environments. Additionally, BPIPP exhibits distinct reaction kinetics, allowing for rapid modulation of signaling pathways in response to cellular stimuli. | ||||||
2′,5′-Dideoxyadenosine | 6698-26-6 | sc-201562 sc-201562A | 5 mg 25 mg | $143.00 $612.00 | 21 | |
2',5'-Dideoxyadenosine functions as an adenylyl cyclase by promoting the synthesis of cyclic AMP from ATP, playing a pivotal role in intracellular signaling. Its unique conformation allows for selective interactions with effector proteins, modulating enzyme activity. The compound's ability to stabilize transition states enhances reaction rates, while its polar characteristics facilitate solubility in aqueous environments, impacting its distribution and functional dynamics within cellular systems. | ||||||
Dihomo-γ-linolenylethanolamide | 150314-34-4 | sc-202137 | 5 mg | $55.00 | ||
Dihomo-γ-linolenylethanolamide acts as an adenylyl cyclase by influencing the conversion of ATP to cyclic AMP, crucial for signal transduction. Its structural features enable specific binding to regulatory proteins, thereby fine-tuning cellular responses. The compound exhibits unique kinetic properties, promoting rapid reaction rates through effective transition state stabilization. Additionally, its hydrophobic regions contribute to membrane interactions, affecting its localization and functional efficacy within lipid environments. | ||||||