Chemical inhibitors of ISOC1 function by impeding various signaling pathways that contribute to the protein's activity within the cell. LY294002 and Wortmannin, for instance, target phosphoinositide 3-kinases (PI3K), which are pivotal in the activation of downstream molecules that can regulate ISOC1 activity. By inhibiting PI3K, these compounds prevent the phosphorylation events necessary for the subsequent activation of proteins involved in the pathways ISOC1 operates in, leading to a decrease in its functional activity. Similarly, PD98059 and U0126 exert their effects by selectively inhibiting mitogen-activated protein kinase kinase (MEK), a kinase that is upstream of the extracellular signal-regulated kinases (ERK). ERK pathways are known to regulate a variety of proteins, and by obstructing the MEK-ERK signaling cascade, PD98059 and U0126 effectively limit the functional activity of ISOC1.
Furthermore, SP600125 inhibits c-Jun N-terminal kinase (JNK), which is involved in regulating responses to stress and inflammation, processes in which ISOC1 may play a role. By blocking JNK, SP600125 can impede the functional activity of ISOC1. SB203580, another chemical inhibitor, targets p38 MAP kinase, which is implicated in the control of a host of proteins, including ISOC1. Inhibition of p38 MAPK by SB203580 can therefore disrupt ISOC1's functional activity. PP2 and Y-27632 are inhibitors of Src family kinases and Rho-associated protein kinase (ROCK), respectively, both of which are involved in signaling pathways that can regulate ISOC1 activity. PP2 and Y-27632 can decrease ISOC1 functional activity by inhibiting these kinases. PD173074 and SU5402 are both FGFR inhibitors that, by blocking FGFR signaling, disrupt downstream signaling pathways critical for ISOC1's function, leading to its inhibition. Lastly, Dorsomorphin and LDN-193189 inhibit AMP-activated protein kinase (AMPK) and BMP signaling, respectively. Since ISOC1's activity may be regulated by these pathways, inhibition by Dorsomorphin and LDN-193189 can lead to a decrease in ISOC1 function.
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