Chemical inhibitors of 1110018G07Rik utilize various intracellular signaling pathways to inhibit its function. Staurosporine operates as a broad-spectrum protein kinase inhibitor, targeting numerous kinases that can phosphorylate and activate 1110018G07Rik, thereby leading to its inhibition. Similarly, Bisindolylmaleimide I selectively inhibits protein kinase C, which is potentially involved in the phosphorylation or regulation of 1110018G07Rik activities. Inhibition by LY294002 and Wortmannin specifically targets the PI3K/AKT pathway, a common regulatory pathway for many proteins, which includes the regulation of 1110018G07Rik. By impeding PI3K, the subsequent decrease in AKT phosphorylation directly affects 1110018G07Rik activity. Rapamycin, through its complex with FKBP12, specifically inhibits the mTOR pathway, another key regulator of protein function, which includes the regulation of 1110018G07Rik.
Further, U0126 and PD98059 are selective inhibitors of the MEK1/2 and MEK respectively, both of which are upstream regulators of the ERK pathway. The ERK signaling pathway is a pivotal pathway for the regulation of many proteins, and its inhibition is likely to affect the function of 1110018G07Rik. SB203580 targets another MAP kinase, p38 MAP kinase, and its inhibition can lead to the reduced function of 1110018G07Rik if p38 MAPK is involved in its regulation. SP600125 inhibits JNK, a kinase that, if involved in the regulation of 1110018G07Rik, would lead to its inhibition upon JNK inhibition. Lastly, Dasatinib and Lapatinib target specific tyrosine kinases such as the Src family kinases, BCR-ABL, EGFR, and HER2, all of which are involved in critical signaling cascades. The inhibition of these kinases by Dasatinib and Lapatinib can result in the direct inhibition of 1110018G07Rik if it is dependent on any of these pathways. PP2, like Dasatinib, is another inhibitor of Src family kinases, indicating that if Src kinases regulate 1110018G07Rik, PP2 would also result in its inhibition.
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