The class of compounds termed PCDHGA5 Activators would be designed to selectively upregulate the activity of the protein product of the PCDHGA5 gene, which is part of the protocadherin gamma subfamily A. Protocadherins are a group of molecules that play significant roles in cell-cell adhesion, the formation of cellular assemblies, and the establishment of precise neural connections. PCDHGA5, like other members of its family, is characterized by its cadherin domains, which are implicated in homophilic cell adhesion interactions. Activators of PCDHGA5 would specifically bind to and increase the activity of this protein, potentially affecting the adhesion properties of cells expressing this protocadherin. The development of such activators would require a thorough understanding of the protein's structure to identify domains that are critical for its adhesive functions. Structural analysis through high-resolution techniques such as X-ray crystallography or cryo-electron microscopy could provide the necessary insights into the binding sites and conformational states that are amenable to activation by small molecules.
In the quest for PCDHGA5 Activators, a multidisciplinary approach involving computational chemistry and experimental pharmacology would be essential. The initial phase would involve using computational tools to model interactions between small molecules and the PCDHGA5 protein, leveraging techniques like molecular docking to predict how these compounds might enhance the protein's activity. Subsequent steps would involve the synthesis of promising compounds followed by in vitro testing to assess their ability to activate PCDHGA5. Such tests would likely include assays to measure direct binding affinity, as well as functional assays to determine the effect of the compounds on cellular adhesion processes. Through an iterative process of design, synthesis, and testing, the chemical structures of these activators could be refined to improve their selectivity and potency as PCDHGA5 modulators. The resulting compounds would be valuable tools for probing the function of PCDHGA5 in cellular models, thereby contributing to a greater understanding of the biological roles of protocadherins in cell-cell adhesion and neural network formation.
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Valproic Acid | 99-66-1 | sc-213144 | 10 g | $85.00 | 9 | |
Valproic acid is an HDAC inhibitor that could potentially lead to chromatin remodeling and affect the expression of genes involved in neural development. | ||||||
Lithium | 7439-93-2 | sc-252954 | 50 g | $214.00 | ||
Lithium can impact glycogen synthase kinase 3 (GSK-3) activity, which might influence Wnt signaling and hence PCDHGA5 expression. | ||||||
Retinoic Acid, all trans | 302-79-4 | sc-200898 sc-200898A sc-200898B sc-200898C | 500 mg 5 g 10 g 100 g | $65.00 $319.00 $575.00 $998.00 | 28 | |
Retinoic acid regulates gene transcription and is crucial for neural development, which could include modulation of PCDHGA5 expression. | ||||||
β-Estradiol | 50-28-2 | sc-204431 sc-204431A | 500 mg 5 g | $62.00 $178.00 | 8 | |
Beta-estradiol can influence neurodevelopment and might regulate the expression of PCDHGA5 through estrogen receptor signaling. | ||||||
(−)-Epigallocatechin Gallate | 989-51-5 | sc-200802 sc-200802A sc-200802B sc-200802C sc-200802D sc-200802E | 10 mg 50 mg 100 mg 500 mg 1 g 10 g | $42.00 $72.00 $124.00 $238.00 $520.00 $1234.00 | 11 | |
EGCG, a component of green tea, has been associated with neuroprotective effects and might affect PCDHGA5 expression. | ||||||
Hydroxyurea | 127-07-1 | sc-29061 sc-29061A | 5 g 25 g | $76.00 $255.00 | 18 | |
Hydroxyurea can cause DNA damage and may influence the expression of genes involved in the DNA damage response, including neural genes like PCDHGA5. | ||||||
Folic Acid | 59-30-3 | sc-204758 | 10 g | $72.00 | 2 | |
Folic acid is crucial for methylation processes and DNA synthesis/repair, which could influence gene expression patterns, including PCDHGA5. |