Chemical inhibitors of 1700022I11Rik can act through various mechanisms to inhibit the functional activity of the protein. Staurosporine and Bisindolylmaleimide I are two such inhibitors; Staurosporine is a broad-spectrum protein kinase inhibitor, which can prevent the phosphorylation activity necessary for the activation of many proteins, including 1700022I11Rik if it is regulated by kinases. Bisindolylmaleimide I specifically targets protein kinase C (PKC), and if 1700022I11Rik's function is regulated through PKC-mediated pathways, this inhibitor can effectively reduce its activity by competing with ATP at the catalytic site of PKC. Similarly, Genistein operates by inhibiting tyrosine kinases, which could affect 1700022I11Rik by preventing necessary phosphorylation on tyrosine residues. The inhibitor PD 98059 selectively targets MEK, a kinase within the ERK pathway, and would inhibit 1700022I11Rik if it is part of this signaling cascade by preventing the phosphorylation and activation of ERK itself.
Another set of inhibitors includes LY294002 and Wortmannin, both of which target phosphoinositide 3-kinases (PI3K). These inhibitors can suppress the activity of 1700022I11Rik by disrupting the PI3K pathway, which is often involved in cell survival and growth signals. Rapamycin, on the other hand, binds to mTOR complex and inhibits its activity, affecting 1700022I11Rik if its function is downstream of mTOR signaling. PP2 is a selective inhibitor for Src family tyrosine kinases. If Src kinases modulate the activity of 1700022I11Rik, then PP2 would result in the inhibition of its function as well. SB203580 and U0126 both serve as MAP kinase inhibitors, with SB203580 targeting p38 MAP kinase and U0126 inhibiting MEK. The inhibition of these kinases would prevent the activation of their respective signaling pathways, leading to the inhibition of 1700022I11Rik if it is a downstream effector. SP600125 inhibits JNK, which could result in the inhibition of 1700022I11Rik if it is involved in pathways related to apoptosis and inflammation that are regulated by JNK. Lastly, ZM-447439 is an Aurora kinase inhibitor, and if 1700022I11Rik plays a role in cell cycle regulation or mitotic processes where Aurora kinases are essential, then its inhibition by ZM-447439 would impair the proper function of 1700022I11Rik.
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