The term PCDHGC Inhibitors refers to a class of chemical compounds that primarily target and modulate the function of a specific group of proteins known as Protocadherin gamma cluster (PCDHGC). These inhibitors are designed with the intention of altering the activity or expression of PCDHGC proteins within biological systems. PCDHGC proteins are a subset of the cadherin superfamily, which plays pivotal roles in various cellular processes, particularly in mediating cell-cell adhesion and communication. Unlike the classical cadherins found in adherens junctions, PCDHGC proteins are expressed predominantly in the nervous system and are involved in neuronal development, synaptic plasticity, and neural circuitry formation.
PCDHGC Inhibitors are developed to modulate these proteins' activities, influencing the intricate processes of neural development and synaptic plasticity. By interfering with the functioning of PCDHGC proteins, these inhibitors can lead to alterations in cell adhesion, impacting neuronal wiring and connectivity. The underlying molecular mechanisms through which PCDHGC Inhibitors exert their effects involve binding to specific regions of PCDHGC proteins, which can disrupt protein-protein interactions or interfere with their downstream signaling pathways. Consequently, the modulation of PCDHGC function by these inhibitors may have implications for understanding neural development, neural plasticity, and perhaps the pathogenesis of certain neurological disorders.
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
---|---|---|---|---|---|---|
Imatinib | 152459-95-5 | sc-267106 sc-267106A sc-267106B | 10 mg 100 mg 1 g | $25.00 $117.00 $209.00 | 27 | |
Inhibits tyrosine kinase activity, targeting BCR-ABL and c-KIT in cancer. | ||||||
Sorafenib | 284461-73-0 | sc-220125 sc-220125A sc-220125B | 5 mg 50 mg 500 mg | $56.00 $260.00 $416.00 | 129 | |
Multi-kinase inhibitor affecting RAF/MEK/ERK and VEGFR/PDGFR in cancer. | ||||||
Gefitinib | 184475-35-2 | sc-202166 sc-202166A sc-202166B sc-202166C | 100 mg 250 mg 1 g 5 g | $62.00 $112.00 $214.00 $342.00 | 74 | |
Blocks EGFR signaling by targeting the ATP-binding site in cancer cells. | ||||||
Rapamycin | 53123-88-9 | sc-3504 sc-3504A sc-3504B | 1 mg 5 mg 25 mg | $62.00 $155.00 $320.00 | 233 | |
Inhibits mTOR, regulating cell growth and autophagy, used in immunosuppression. | ||||||
Taxol | 33069-62-4 | sc-201439D sc-201439 sc-201439A sc-201439E sc-201439B sc-201439C | 1 mg 5 mg 25 mg 100 mg 250 mg 1 g | $40.00 $73.00 $217.00 $242.00 $724.00 $1196.00 | 39 | |
Disrupts microtubule function, blocking cell division. | ||||||
Dasatinib | 302962-49-8 | sc-358114 sc-358114A | 25 mg 1 g | $47.00 $145.00 | 51 | |
Inhibits multiple tyrosine kinases, including BCR-ABL and Src in cancer. | ||||||
Erlotinib Hydrochloride | 183319-69-9 | sc-202154 sc-202154A | 10 mg 25 mg | $74.00 $119.00 | 33 | |
Targets EGFR by competing for ATP binding, used in cancer therapy. | ||||||
Bortezomib | 179324-69-7 | sc-217785 sc-217785A | 2.5 mg 25 mg | $132.00 $1064.00 | 115 | |
Inhibits the proteasome, disrupting protein degradation in multiple myeloma. | ||||||
Sunitinib Malate | 341031-54-7 | sc-220177 sc-220177A sc-220177B | 10 mg 100 mg 3 g | $193.00 $510.00 $1072.00 | 4 | |
Inhibits multiple kinases, including VEGFR and PDGFR in cancer therapy. | ||||||
Vemurafenib | 918504-65-1 | sc-364643 sc-364643A | 10 mg 50 mg | $115.00 $415.00 | 11 | |
Targets BRAF kinase in melanoma with the V600E mutation. |