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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B7598 Phorbol 12,13-dibutyrateSummary: A protein kinase C (PKC) activator -
B7595 Bisindolylmaleimide IISummary: protein kinase C (PKC) inhibitor -
B7272 FR 2369241 CitationSummary: PKC-ε activator, selective -
B7056 CGP 53353Summary: PKCβII inhibitor -
B7033 Bryostatin 11 CitationSummary: PKC activator -
B6807 Calphostin CSummary: protein kinase C inhibitor -
B6803 Rottlerin1 CitationTarget: PKC|Ca2 /calmodulin-dependent protein kinases (CaMKs)|PRAK|MAPKAP-K2Summary: PKC inhibitor -
B6798 Ro 32-0432 hydrochlorideSummary: protein kinase C inhibitor -
B6385 D-erythro-Sphingosine (synthetic)Summary: protein kinase C and calmodulin-dependent enzymes inhibitor -
B6343 C-1Summary: protein kinase C inhibitor
