TGF-β/Smad Signaling


The TGF-β family is generally classified into two sub-families, TGF-β ligands, and bone morphogenic protein (BMP) ligands. In canonical signaling, receptor activation lead to phosphorylation of a group of transcription factors called Smads. TGF-β ligands bind to type II receptors (TGF-β II) which recruit and phosphorylate type I receptor (TGF-β I) on serine/threonine residues. The TGF-β I then recruits and phosphorylates a receptor regulated Smad (R-Smad). The R-Smad binds to the common Smad (Co-Smad) and forms a heterodimeric complex. This complex then translocates into the cell nucleus where it binds with nuclear co-factors to regulate the transcription of various target genes. Dysregulation of TGF-β/Smad signaling pathway is associated with a number of pathological conditions including fibrosis, cancer, immunodeficiency, diabetes and cardiovascular diseases etc.
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A8301 GW788388Summary: ALK5 inhibitor, potent and selective -
A8310 PF-5622711 CitationTarget: FAK|Pyk2Summary: ATP-competitive FAK inhibitor, reversible -
A8324 LDN-1931898 CitationTarget: BMP and Other Activin ReceptorsSummary: ALK inhibitor,potent and selective -
A8348 LY21572992 CitationSummary: TGF-βR1 inhibitor,potent and selective -
A8345 PF-562271 HClTarget: FAK|Pyk2Summary: FAK/Pyk2 inhibitor -
A8341 Go 6976Target: PKCSummary: PKCα/PKCβ1 inhibitor -
A8342 GF 109203X1 CitationTarget: PKCSummary: Protein kinase C,MLCK,PKG and PKA inhibitor -
A8343 Go 69831 CitationSummary: pan-PKC inhibitor -
A8344 K-252cTarget: PKC|PKASummary: Protein kinase inhibitor -
A8464 LY210976110 CitationSummary: TβRI/II kinase inhibitor

