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.
- B3709 Midostaurin (PKC412)Target: PKC|PKA|KDR|Flk1|PPK|c-Syk|CDK1/CyclinBSummary: PKC inhibitor
- B6385 D-erythro-Sphingosine (synthetic)Summary: protein kinase C and calmodulin-dependent enzymes inhibitor
- B6798 Ro 32-0432 hydrochlorideSummary: protein kinase C inhibitor
- B6807 Calphostin CSummary: protein kinase C inhibitor
- B7033 Bryostatin 11 CitationSummary: PKC activator
- B7056 CGP 53353Summary: PKCβII inhibitor
- B7272 FR 2369241 CitationSummary: PKC-ε activator, selective
- B7598 Phorbol 12,13-dibutyrateSummary: A protein kinase C (PKC) activator
- B7704 LY 333531 hydrochlorideSummary: PKCβ inhibitor
- B5172 Pseudo RACK1Summary: Activator of protein kinase C