Chemical inhibitors of E430002G05Rik function by interacting with various signaling pathways and molecular processes that are essential for the protein's activity. SB-3CT, for instance, targets matrix metalloproteinases (MMPs), particularly MMP-2 and MMP-9, which play a role in extracellular matrix remodeling. By inhibiting these MMPs, SB-3CT can reduce the degradation of the extracellular matrix, potentially affecting the signaling pathways that E430002G05Rik is part of. Along a similar vein, PD 98059 and U0126 act upon the MAPK/ERK pathway by inhibiting MEK, which is instrumental in cell signaling related to proliferation and differentiation. The inhibition by these chemicals can suppress the pathway's activity, leading to a decrease in E430002G05Rik-related functions.
Other inhibitors, such as LY294002 and Wortmannin, exert their effects by inhibiting phosphatidylinositol 3-kinase (PI3K), a key player in growth and survival signaling pathways. The suppression of PI3K activity by these inhibitors can lead to a decrease in the functional activity of E430002G05Rik if it is involved in PI3K-dependent processes. SP600125, by inhibiting c-Jun N-terminal kinase (JNK), can disrupt cellular processes like apoptosis and inflammation, which may involve E430002G05Rik. SB202190 targets p38 MAP kinase, influencing cell differentiation, apoptosis, and autophagy, which could interfere with E430002G05Rik's role in these processes. GF109203X's inhibition of protein kinase C (PKC) and PP2's inhibition of Src-family tyrosine kinases can also indirectly suppress E430002G05Rik's function by blocking the respective kinases' signal transduction pathways. Lastly, Y-27632 and Dorsomorphin target Rho-associated protein kinase (ROCK) and AMP-activated protein kinase (AMPK) respectively, along with BMP signaling, which can lead to an indirect decrease in E430002G05Rik activity if the protein is associated with pathways regulated by these kinases.
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