CDRT15L2 inhibitors are apart of part of the PI3K/AKT pathway, compounds such as LY294002 and Wortmannin can act by hindering PI3K activity, thereby attenuating subsequent AKT phosphorylation and activity. In the case of involvement in the MAPK/ERK pathway, MEK inhibitors like U0126 and PD98059 can disrupt the pathway, which might indirectly reduce CDRT15L2 activity if it is regulated by or regulating this pathway.
Compounds like Rapamycin and Bortezomib operate on a broader scale, with Rapamycin inhibiting mTOR, a key regulator of cell growth and proliferation, and Bortezomib impairing proteasome function, which could lead to increased levels of proteins, including possibly CDRT15L2, if it is prone to degradation by the ubiquitin-proteasome system. Other compounds listed may affect kinases such as Src or JNK, which are involved in various signaling cascades, or proteins such as ROCK that play roles in cytoskeletal organization. Inhibitors like Dasatinib, PP2, and SP600125 would thus be relevant if CDRT15L2 is part of or regulated by these pathways.
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