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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A3642 NarciclasineSummary: Modulates the Rho/ROCK/LIM kinase/cofilin pathway
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A3658 NG25Summary: TAK1 inhibitor
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A3660 Nilotinib monohydrochloride monohydrateSummary: Bcr-Abl inhibitor
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A3754 RepSoxSummary: ALK5 inhibitor,potent and selective
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A3771 RKI-1447Target: ROCKSummary: Potent ROCK1/ROCK2 inhibitor
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A3799 SB-505124 hydrochlorideTarget: ALKSummary: ALK5/ALK4/ALK7 inhibitor in TGF-β/activin signalling,selective
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A3808 SD-208Summary: TGF-βR I kinase inhibitor
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A3825 SLx-21191 CitationTarget: ROCKSummary: Selective ROCK2 inhibitor
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A3132 A 77-01Summary: Potent ALK5 inhibitor
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A3133 A 83-01Summary: ALK-5 inhibitor