Date published: 2025-10-11

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NumbL Inhibitors

Chemical inhibitors of NumbL can target various signaling pathways with which this protein is associated to achieve functional inhibition. LY294002 and Wortmannin are inhibitors of phosphoinositide 3-kinases (PI3Ks), which play a significant role in the PI3K/Akt signaling pathway. Given that NumbL interacts within this pathway, these inhibitors can lead to a reduction in Akt phosphorylation, a necessary step for NumbL to mediate its cellular effects. Similarly, Rapamycin and PP242 directly inhibit mTOR, a downstream component of the PI3K/Akt/mTOR pathway. Inhibition of mTOR results in decreased signaling potential, thereby limiting the functional contributions of NumbL in this pathway. PF-4708671, by selectively inhibiting p70 ribosomal S6 kinase 1 (S6K1), operates further downstream in the same PI3K/Akt pathway, leading to reduced phosphorylation of S6K1's targets and therefore diminishing NumbL's functional activity.

In addition to the PI3K/Akt/mTOR pathway, NumbL's function can be inhibited through disruption of the MAPK/ERK pathway. U0126, PD98059, and SL327 are selective inhibitors of MEK1/2, which act upstream of ERK. These inhibitors prevent ERK activation, thereby inhibiting downstream signaling that involves NumbL. SB203580 and BIX 02189 target other kinases within the MAPK pathway, namely p38 MAP kinase and MEK5, respectively. By disrupting these kinases' activities, they prevent the phosphorylation and activation of downstream effectors that would otherwise interact with NumbL. SP600125's inhibition of c-Jun N-terminal kinase (JNK) also serves to inhibit the MAPK pathway, affecting the cellular processes in which NumbL is involved. Lastly, AZD8055, a potent inhibitor of both mTORC1 and mTORC2 complexes, disrupts the PI3K/Akt/mTOR pathway at multiple levels, offering a broad inhibition of NumbL's role within this signaling cascade.

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