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.
-   A3310 chroman 11 CitationSummary: ROCK II inhibitor, highly potent and selective A3310 chroman 11 CitationSummary: ROCK II inhibitor, highly potent and selective
-   A3754 RepSoxSummary: ALK5 inhibitor,potent and selective A3754 RepSoxSummary: ALK5 inhibitor,potent and selective
-   A2133 Saracatinib (AZD0530)3 CitationTarget: SrcSummary: Src/Abl inhibitor,potent and selective A2133 Saracatinib (AZD0530)3 CitationTarget: SrcSummary: Src/Abl inhibitor,potent and selective
-   A8345 PF-562271 HClTarget: FAK|Pyk2Summary: FAK/Pyk2 inhibitor A8345 PF-562271 HClTarget: FAK|Pyk2Summary: FAK/Pyk2 inhibitor
-   A1352 Zoledronic AcidTarget: Farnesyl Diphosphate SynthasesSummary: Potent nitrogen-containing bisphosphonates A1352 Zoledronic AcidTarget: Farnesyl Diphosphate SynthasesSummary: Potent nitrogen-containing bisphosphonates
-   A3008 Y-27632 dihydrochloride67 CitationTarget: ROCKSummary: ROCK inhibitor A3008 Y-27632 dihydrochloride67 CitationTarget: ROCKSummary: ROCK inhibitor
-   A3132 A 77-01Summary: Potent ALK5 inhibitor A3132 A 77-01Summary: Potent ALK5 inhibitor
-   A3658 NG25Summary: TAK1 inhibitor A3658 NG25Summary: TAK1 inhibitor
-   A3545 LDN193189 Hydrochloride1 CitationSummary: ALK inhibitor,potent and selective A3545 LDN193189 Hydrochloride1 CitationSummary: ALK inhibitor,potent and selective
-   A1805 Imatinib Mesylate (STI571)Target: PDGFR|c-Kit|Bcr-AblSummary: Abl/c-kit/PDGFR inhibitor A1805 Imatinib Mesylate (STI571)Target: PDGFR|c-Kit|Bcr-AblSummary: Abl/c-kit/PDGFR inhibitor
