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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B4964 (-)-epicatechinSummary: inducer of pancreatic β-cell regeneration
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B4965 (-)-epicatechin gallateSummary: major catechin in green tea
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B5858 ITD 1Summary: The first selective TGFβ inhibitor
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B5946 EW-71971 CitationTarget: BMP and Other Activin ReceptorsSummary: Selective inhibitor of TGF-β type I receptor kinase
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B5965 Tamoxifen1 CitationTarget: PKCSummary: TGF-β modulatory and PKC inhibitory effects
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A3306 Chelerythrine ChlorideTarget: PKCSummary: PKC antagonist
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A3310 chroman 11 CitationSummary: ROCK II inhibitor, highly potent and selective
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A3478 HydroxyfasudilTarget: ROCK|Rho-kinaseSummary: Rho-kinase inhibitor and vasodilator
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A3479 Hydroxyfasudil hydrochlorideSummary: Rho-kinase inhibitor and vasodilator
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A3545 LDN193189 Hydrochloride1 CitationSummary: ALK inhibitor,potent and selective