Chemical inhibitors of 1700014B07Rik can influence the activity of this protein through various mechanisms, each related to the inhibition of specific kinases and signaling pathways. Staurosporine, a broad-spectrum kinase inhibitor, can hinder the activity of 1700014B07Rik by competing with ATP for binding to its active site, a common mechanism for kinase inhibition. Similarly, Bisindolylmaleimide I, as a specific inhibitor of protein kinase C, can disrupt the regulatory phosphorylation events that 1700014B07Rik may undergo, effectively reducing its kinase activity. LY294002 and Wortmannin, both potent inhibitors of phosphoinositide 3-kinases, can alter the PI3K/AKT pathway, leading to reduced activity of downstream proteins, which may include 1700014B07Rik if it is part of this signaling cascade. PD98059 and U0126 target MEK1/2, which are upstream of MAPK/ERK kinases; inhibition here can result in decreased activation of 1700014B07Rik if it is regulated by this pathway. Rapamycin acts upon mTORC1 within the mTOR signaling pathway, and its inhibition can suppress the functions of downstream proteins, potentially including 1700014B07Rik.
Further affecting the activity of 1700014B07Rik, SB203580 can selectively inhibit p38 MAPK, which could decrease the kinase activity of 1700014B07Rik if it is part of the p38 MAPK signaling. PP2, as a selective inhibitor of Src family kinases, can interfere with signaling pathways that 1700014B07Rik may be involved in, particularly if it is regulated by Src kinase-mediated phosphorylation. SP600125's inhibition of JNK from the MAPK family can disrupt processes that govern cellular proliferation, which may include the regulatory functions of 1700014B07Rik. Additionally, ZM-447439 and AZD1152-HQPA target Aurora kinases; the former is a broad inhibitor of these kinases, while the latter is selective for Aurora B kinase. Inhibition of Aurora kinases can disrupt cell cycle progression and mitosis, affecting the activity of 1700014B07Rik if it plays a role in these cellular events governed by Aurora kinase activity.
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