Table 1.
Pharmacological Inhibitor | Function |
---|---|
Actinomycin D | Transcription inhibitor: Binds DNA at the transcription initiation complex and prevents elongation of RNA chain by RNA polymerase. |
AG1296 | Inhibitor of PDGFR: Inhibits the phosphorylation of autophosphorylation sites of the PDGFR. |
Akt inhibitor VIII | Inhibitor of Akt: An allosteric inhibitor of Akt1 and Akt2 that less effectively blocks Akt3 activity. |
Cycloheximide | Translation inhibitor: Inhibits translation elongation through binding to the E-site of the 60S ribosomal unit and interfering with deacetylated tRNA. |
c-Src inhibitor II | Inhibitor of c-Src: A potent, selective, reversible, and ATP-competitive inhibitor of Src family tyrosine kinases. |
LY294002 | Inhibitor of PI3K: Inhibits PI3K activity via competitive inhibition of an ATP binding site on the p85α subunit. |
PF431396 | Inhibitor of Pyk2: An ATP-competitive inhibitor of PYK2/FAK (focal adhesion kinase). |
p38 MAPK inhibitor VIII | Inhibitor of p38 MAPK: Inhibits p38α and p38β MAP kinase. |
SP600125 | Inhibitor of JNK1-3: A reversible ATP-competitive inhibitor. |
Tanshinone IIA | Inhibitor of AP-1: Inhibits AP-1 activity by suppressing jun-fos (members of the transcription factor AP-1 family)-DNA complex formation. |