Chemical inhibitors of ICAM-5 operate through various mechanisms to impair the functional activity of this cell adhesion molecule. TAPI-0 and GM6001 effectively inhibit the proteolytic shedding of ICAM-5, which is a crucial step for its function in cellular signaling pathways. TAPI-0 acts specifically by targeting ADAM17, a disintegrin and metalloproteinase responsible for the cleavage of ICAM-5's extracellular domain. GM6001, as a broad-spectrum matrix metalloprotease inhibitor, also impedes the shedding of ICAM-5, maintaining it in a form that is less active in cell-cell adhesion processes. Similarly, chemicals like PD98059, U0126, and LY303511 target the MAPK/ERK and PI3K/Akt pathways respectively, which are upstream regulators of ICAM-5. By inhibiting MEK, PD98059 and U0126 prevent the phosphorylation and activation of ERK1/2, which are known to be involved in the regulation of ICAM-5-mediated signaling. LY303511, akin to LY294002, suppresses PI3K activity, leading to reduced Akt activation and subsequent dampening of ICAM-5 signaling capabilities.
Additionally, SB203580 and SP600125 target other members of the MAPK family, namely p38 MAPK and JNK. SB203580's inhibition of p38 MAPK alters the phosphorylation dynamics of ICAM-5, which may negatively influence the protein's signaling and adhesive functions. SP600125 hinders JNK, which can suppress JNK-mediated phosphorylation events associated with ICAM-5. PP2, a Src family kinase inhibitor, can impede Src-mediated phosphorylation of ICAM-5, which is essential for its activity in cellular signaling. AG490's inhibition of JAK2 kinase can also interfere with the phosphorylation state of ICAM-5, thus inhibiting its interaction with other cellular components. BAY 11-7082, which inhibits NF-κB activation, may indirectly decrease the functional activity of ICAM-5 by reducing the expression of molecules that are regulated by NF-κB and are essential for the full functional activity of ICAM-5 in cellular processes. Collectively, these inhibitors disrupt the signaling and adhesive functions of ICAM-5 by targeting various enzymes and pathways that are essential for its activation and function.
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