C17orf85 inhibitors consits of Staurosporine and LY294002 inhibit kinases within the cell, which can have downstream effects on multiple signaling pathways that may intersect with C17orf85's function. Rapamycin specifically inhibits the mTOR pathway, a central regulator of cell growth and metabolism, which could influence the activity or expression of C17orf85.
Trichostatin A and 5-Azacytidine act epigenetically to modulate gene expression. By inhibiting histone deacetylases and DNA methyltransferases, respectively, they can alter the chromatin structure and thereby affect the expression of a broad range of genes, including possibly C17orf85. PD98059, SB203580, and SP600125 target different MAP kinases, which are important in regulating cell proliferation, apoptosis, and stress responses. The inhibition of these kinases can lead to changes in cellular processes that C17orf85 may be a part of. Calcium signaling, which is crucial for many cellular functions including cell cycle control and apoptosis, can be affected by the calmodulin inhibitor W7 and the calcium chelator BAPTA-AM.
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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2-Deoxy-D-glucose | 154-17-6 | sc-202010 sc-202010A | 1 g 5 g | $65.00 $210.00 | 26 | |
A glycolysis inhibitor which can alter energy metabolism in cells, potentially affecting C17orf85 activity. | ||||||
FCCP | 370-86-5 | sc-203578 sc-203578A | 10 mg 50 mg | $92.00 $348.00 | 46 | |
A protonophore that disrupts mitochondrial membrane potential, possibly influencing C17orf85 function. |