Table 1.
Multiple protein kinase inhibitors did not prevent PKD1 phosphorylation at Ser203 in IEC-18 cells
Confluent cultures of IEC-18 cells were incubated with each of the inhibitors listed below for 1 h. Then the cells were stimulated with ANG II for 60 min and lysed, and the phosphorylation of PKD1 at Ser203 was determined by immunoblotting using the antibody that detects the phosphorylated state of this residue. The inhibitors listed in this table did not prevent Ser203 phosphorylation at the concentrations tested. cPKC, conventional PKCs; nPKC, novel PKCs; aPKC, atypical PKCs; and mTOR, mechanistic target of rapamycin.
Inhibitor | Primary target | Concentration |
---|---|---|
μm | ||
kb NB 142–70 | PKD | 1–10 |
CRT 0066101 | PKD | 1–5 |
Go6983 | cPKC, nPKC, aPKC | 1–10 |
GF 109203X | cPKC, nPKC | 3.5 |
KT 5720 | PKA | 1 |
KU 0063794 | mTOR | 1–5 |
GSK 690693 | Akt, PKC, PKA | 1–5 |
KU 55933 | ATM | 5–25 |
HA 1077 | ROCK-II, PKA, PKG, PKCα | 10 |
Y-27632 | ROCK | 10 |
Compound C | AMPK | 5–25 |
Aurora kinase inhibitor III | Aurora A | 10 |
Aurora kinase inhibitor II | Aurora A and B | 10 |
GSK-3 inhibitor XVI | GSK-3 | 5 |
LY 294002 | PI3K, mTOR | 10 |
PP2 | Src | 10 |
AG1478 | EGFR | 1 |
U0126 | MEK1/2 | 5 |
PD98059 | MEK1/2 | 5 |
PIM-1 inhibitor 2 | Pim-1 kinase | 1–10 |
TG003 | Clk family | 1–10 |
Enzastaurin (LY317615) | PKCβ | 1–5 |
GO6976 | cPKC, PKD | 10 |
KN92 | CaMKII | 10 |
KN62 | CaMKII | 10 |
FAK inhibitor 14 | FAK | 1–5 |
UCN-01 | Chk1 | 10 |