Date published: 2025-9-21

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TBX22 Inhibitors

Chemical inhibitors of TBX22 can interfere with the protein's function by targeting various signaling pathways that are crucial for its activity. SB-431542, LY364947, A-83-01, RepSox, SB-505124, Galunisertib, and EW-7197, are molecules that inhibit the TGF-β signaling pathway at different points. SB-431542, A-83-01, and RepSox specifically inhibit ALK5, ALK4, and ALK7 receptors, which are integral to the TGF-β pathway that TBX22 utilizes. LY364947 and Galunisertib, on the other hand, target TGFβR-I, a receptor whose activity is necessary for TBX22's role in cellular processes. SB-505124 also falls into this category, selectively inhibiting ALK4, ALK5, and ALK7 receptors within the same pathway. EW-7197 further contributes to the inhibition of TBX22 by selectively targeting the TGF-β type I receptor ALK5 kinase. By inhibiting these receptors or kinases, these chemicals disrupt the signaling cascade, preventing TBX22 from carrying out its function within the pathway.

Conversely, Dorsomorphin, LDN-193189, DMH1, LDN-214117, and K02288 act upon the bone morphogenetic protein (BMP) signaling pathway, which is another route through which TBX22 can mediate its effects. Dorsomorphin and DMH1 are inhibitors that suppress BMP signaling, which is essential for the TBX22's involvement in craniofacial development. LDN-193189 and LDN-214117 are more selective, targeting BMP type I receptors that participate in TBX22's action in development. K02288 extends this inhibition by targeting a range of BMP type I receptors, including ALK1, ALK2, ALK3, and ALK6, all of which are necessary for the signaling that TBX22 requires. By blocking these critical receptors, these chemicals can effectively inhibit the functionality of TBX22, thereby inhibiting the signaling events TBX22 needs to exert its effects on cellular processes.

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