GPR156 Activators represent a unique class of chemical compounds engineered to selectively enhance the activity of GPR156, a member of the G protein-coupled receptor (GPCR) family. GPCRs are integral membrane proteins that play vital roles in cellular signaling, transducing extracellular signals into intracellular responses. The exact function and ligand specificity of GPR156 remain areas of active research, making the development of GPR156 Activators an intriguing endeavor in elucidating the receptor's biological roles. These activators are synthesized through sophisticated chemical processes, with the aim of producing molecules that can specifically interact with GPR156, potentially influencing its natural signaling pathways or uncovering its endogenous ligands. Designing effective GPR156 Activators requires a deep understanding of the receptor's structure, including its transmembrane domains and any potential ligand-binding sites that may be targeted for modulation.
The exploration of GPR156 Activators involves a multidisciplinary research approach, integrating techniques from pharmacology, molecular biology, and structural biology to understand how these compounds interact with GPR156. Scientists employ functional assays, including cAMP assays or calcium mobilization assays, to assess the impact of activators on GPR156-mediated signaling and downstream responses. Structural studies, such as homology modeling and molecular docking, are instrumental in predicting the binding sites and potential interactions between GPR156 and activators. These studies guide the rational design and optimization of activators for increased specificity and efficacy. Additionally, cell-based assays and in vitro systems are utilized to further dissect the receptor's function and evaluate the influence of activators on GPR156-mediated cellular processes. Through this comprehensive research framework, the study of GPR156 Activators aims to advance our understanding of GPCR biology, the functional significance of GPR156, and the intricacies of cellular signaling pathways mediated by this receptor, contributing to the broader field of receptor pharmacology and molecular signaling.
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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3,3′-Diindolylmethane | 1968-05-4 | sc-204624 sc-204624A sc-204624B sc-204624C sc-204624D sc-204624E | 100 mg 500 mg 5 g 10 g 50 g 1 g | $36.00 $64.00 $87.00 $413.00 $668.00 $65.00 | 8 | |
DIM, derived from indole-3-carbinol, can influence gene expression through modulation of the aryl hydrocarbon receptor pathway. | ||||||
Kaempferol | 520-18-3 | sc-202679 sc-202679A sc-202679B | 25 mg 100 mg 1 g | $97.00 $212.00 $500.00 | 11 | |
Kaempferol is a flavonoid that can affect gene expression by interacting with various signaling pathways and transcription factors. |