Chemical inhibitors of 1700020N15Rik act predominantly through the interruption of vital signaling pathways and cell cycle regulation mechanisms that are essential for the protein's function. Palbociclib and its alternative name, PD0332991, are selective inhibitors targeting the cyclin-dependent kinases CDK4 and CDK6. These kinases play a crucial role in the progression of the cell cycle, and their inhibition directly prevents the advancement of the cell cycle phases, wherein 1700020N15Rik is active. Similarly, other chemicals like Omipalisib, AZD8055, and Torin 1, focus on the PI3K/mTOR pathways, which are intricately related to the activities and regulation of 1700020N15Rik. Omipalisib, serving as a dual PI3K/mTOR inhibitor, and AZD8055 and Torin 1, as mTOR specific inhibitors, all lead to the disruption of the downstream signaling necessary for 1700020N15Rik's activity within cellular processes.
Moreover, compounds such as PP242, KU-0063794, and WYE-125132, which are also mTOR inhibitors, function by obstructing the kinase activity of mTOR. This action effectively hampers the signaling pathways that 1700020N15Rik is a part of, thereby inhibiting the protein's function. Rapamycin, another mTOR pathway inhibitor, employs a slightly different approach by forming a complex with FKBP12 that specifically inhibits mTORC1, a complex that is vital for mTOR pathway signaling and 1700020N15Rik's role within it. AZD2014 extends this inhibition to both mTORC1 and mTORC2 complexes, which are essential for proper signaling and function of 1700020N15Rik. GSK2126458, with its high selectivity towards PI3K and mTOR, and OSI-027, a dual mTORC1 and mTORC2 inhibitor, likewise inhibit the necessary signaling pathways, ensuring the functional inhibition of 1700020N15Rik. Each of these chemicals, through their targeted actions, ensures that the critical pathways and processes that 1700020N15Rik is involved in are effectively disrupted, leading to the inhibition of its function within the cell.
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