Date published: 2025-10-13

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ILT-1 Inhibitors

Chemicals classified as ILT-1 inhibitors would be those that interact with or modulate the function of the immune receptor ILT-1, which is implicated in the regulation of immune responses. Since direct inhibitors of ILT-1 are not established, the chemical class encompasses a variety of compounds that can indirectly affect ILT-1 by targeting signaling pathways and cellular processes related to its activity.

These inhibitors include small molecule tyrosine kinase inhibitors like dasatinib and imatinib, which are known to broadly impact tyrosine phosphorylation cascades that could be central to ILT-1 signaling. Compounds such as erlotinib, which target the EGFR pathway, and rapamycin, which acts on mTOR, can have profound effects on cell growth and immune responses, potentially altering ILT-1 related activities. Moreover, the inhibition of specific kinases such as PI3K by LY294002 and wortmannin, MEK by U0126 and PD98059, p38 MAPK by SB203580, Src family kinases by PP2, and JNK by SP600125 could lead to the modulation of numerous immune cell functions. These effects might extend to the pathways in which ILT-1 is involved, despite the absence of direct interaction with the receptor. Finally, BAY 11-7082 serves as an inhibitor of NF-κB, a transcription factor that is pivotal in regulating immune response and inflammation. By inhibiting NF-κB, BAY 11-7082 may influence the expression and function of ILT-1.

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