PCDHGB2 inhibitors are a class of chemical compounds that specifically target protocadherin gamma-B2 (PCDHGB2), a member of the protocadherin family, which plays a critical role in cell-cell adhesion, particularly in the nervous system. PCDHGB2 is part of the gamma subfamily of protocadherins, a large group of proteins involved in the regulation of neural development, synaptic formation, and maintenance of neuronal connections. These proteins contribute to the organization and patterning of neural circuits by mediating homophilic interactions between cells, influencing both the architecture of neural tissues and intercellular communication. By inhibiting PCDHGB2, these compounds interfere with its role in maintaining proper cell adhesion, leading to potential changes in how cells, particularly neurons, interact and form networks.
The mechanism of action for PCDHGB2 inhibitors involves binding to the extracellular domains or other functional regions of the protein, blocking its ability to engage in cell-cell adhesion processes. This inhibition disrupts the homophilic binding necessary for the formation of stable cellular connections, which can alter tissue organization and signal transduction pathways. PCDHGB2 inhibitors are valuable research tools for exploring how protocadherins, especially those in the gamma family, contribute to neural patterning and the establishment of complex neural networks. By blocking PCDHGB2 activity, researchers can gain insights into the molecular mechanisms that underlie neural development, synaptic specificity, and the maintenance of cell adhesion in the nervous system. This class of inhibitors helps to elucidate the broader functions of protocadherins in cell signaling and tissue organization, highlighting their essential roles in maintaining proper cellular architecture.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
EGTA | 67-42-5 | sc-3593 sc-3593A sc-3593B sc-3593C sc-3593D | 1 g 10 g 100 g 250 g 1 kg | $20.00 $62.00 $116.00 $246.00 $799.00 | 23 | |
Chelates calcium, which is essential for cadherin function. | ||||||
LY 294002 | 154447-36-6 | sc-201426 sc-201426A | 5 mg 25 mg | $121.00 $392.00 | 148 | |
PI3K inhibitor. PI3K signaling is involved in cadherin-mediated adhesion. | ||||||
Wortmannin | 19545-26-7 | sc-3505 sc-3505A sc-3505B | 1 mg 5 mg 20 mg | $66.00 $219.00 $417.00 | 97 | |
Another PI3K inhibitor affecting cadherin-related signaling. | ||||||
PD 98059 | 167869-21-8 | sc-3532 sc-3532A | 1 mg 5 mg | $39.00 $90.00 | 212 | |
MEK inhibitor; affects MAPK/ERK pathway which can modulate cadherin functions. | ||||||
Y-27632, free base | 146986-50-7 | sc-3536 sc-3536A | 5 mg 50 mg | $182.00 $693.00 | 88 | |
ROCK inhibitor. Rho-associated kinases influence cadherin-based cell adhesion. | ||||||
SP600125 | 129-56-6 | sc-200635 sc-200635A | 10 mg 50 mg | $40.00 $150.00 | 257 | |
JNK inhibitor; JNK pathway can influence cadherin-related processes. | ||||||
SB 203580 | 152121-47-6 | sc-3533 sc-3533A | 1 mg 5 mg | $88.00 $342.00 | 284 | |
p38 MAPK inhibitor; p38 can affect cadherin stabilization and functions. | ||||||
(±)-Blebbistatin | 674289-55-5 | sc-203532B sc-203532 sc-203532A sc-203532C sc-203532D | 5 mg 10 mg 25 mg 50 mg 100 mg | $179.00 $307.00 $455.00 $924.00 $1689.00 | 7 | |
Myosin II inhibitor; can affect cadherin-mediated cell adhesion dynamics. | ||||||
Manumycin A | 52665-74-4 | sc-200857 sc-200857A | 1 mg 5 mg | $215.00 $622.00 | 5 | |
Ras inhibitor; Ras signaling can affect cadherin-mediated cell adhesion. | ||||||
H-1152 dihydrochloride | 451462-58-1 | sc-203592 sc-203592A | 1 mg 5 mg | $102.00 $357.00 | 7 | |
Another ROCK inhibitor which can influence cadherin-mediated cell adhesion processes. | ||||||