T7648 |
HA-100
|
84468-24-6
|
99.69%
|
|
HA-100 is an inhibitor of protein kinase
|
T6304 |
AT7867
|
857531-00-1
|
99.65%
|
|
AT7867 is a potent ATP-competitive inhibitor of Akt1/2/3 and p70S6K/PKA with IC50 of 32 nM/17 nM/47 nM and 85 nM/20 nM, respectively; little activity outside the...
|
T3050 |
ML-7 hydrochloride
|
110448-33-4
|
99.61%
|
|
ML-7 hydrochloride (ML-7 HCl) is a cell-permeable, reversible, effective, ATP-competitive, and specific inhibitor of myosin light chain kinase (Ki: 300 nM); also...
|
T75888 |
PKA Inhibitor Fragment (6-22) amide TFA
|
|
99.61%
|
|
PKA Inhibitor Fragment (6-22) amide TFA (PKA Inhibitor Fragment (6-22) amide TFA) is an inhibitor of the highly potent cAMP-dependent protein kinase A (PKA) inhi...
|
T1418 |
Bucladesine sodium
|
16980-89-5
|
99.58%
|
|
Bucladesine sodium (DC2797) is a cAMP analog with cell-permeable properties. Bucladesine sodium is also a cAMP-dependent protein kinase (PKA) activator and a pho...
|
T6139L |
A-674563 2HCl(552325-73-2(fb-2hcl))
|
T6139L
|
99.57%
|
|
A-674563 2HCl is an Akt1 inhibitor with Ki of 11 nM, modest potent to PKA and >30-fold selective for Akt1 over PKC.
|
T3060 |
Fasudil hydrochloride
|
105628-07-7
|
99.54%
|
|
Fasudil hydrochloride (HA-1077) is a potent inhibitor of ROCK1, PKA, PKC, and MLCK with Ki of 0.33 μM, 1.0 μM, 9.3 μM and 55 μM, respectively.
|
T19836 |
2-Aminopurine
|
452-06-2
|
99.51%
|
|
2-Aminopurine is a double-stranded RNA-dependent protein kinase, protein kinase R (PKR) inhibitor.
|
TP1957L |
PKI (5-24) Acetate(99534-03-9 free base)
|
TP1957L
|
99.47%
|
|
PKI (5-24) Acetate is a high affinity PKA inhibitor (Ki = 2.3 nM).
|
T5065 |
GUANOSINE 3':5'-CYCLIC MONOPHOSPHATE SOD
|
40732-48-7
|
99.44%
|
|
GUANOSINE 3':5'-CYCLIC MONOPHOSPHATE SOD (cGMP sodium salt) , also known as cGMP, is a cellular regulatory agent and has been described as a second messenger. It...
|
T6250 |
H-89 dihydrochloride
|
130964-39-5
|
99.4%
|
|
H-89 dihydrochloride (5-Isoquinolinesulfonamide) is a potent inhibitor of protein kinase A (PKA; IC50: 0.14 μM, Ki: 48 nM).
|
T0610 |
Piceatannol
|
10083-24-6
|
99.39%
|
|
Piceatannol (Astringenin) is an anti-inflammatory, immunomodulatory and antiproliferative agent. It inhibits p56lck and syk protein tyrosine kinases and inhibits...
|
T1837 |
BX-912
|
702674-56-4
|
99.34%
|
|
BX-912 is a specific inhibitor of 3-Phosphoinositide-dependent Kinase-1 (PDK1, IC50: 12 nM). The selectivity of BX-912 is more 10 fold than C-Kit, EGFR, PKA, PKC...
|
T77504 |
JAK1/2/3 Inhibitor 1
|
16234-14-3
|
99.32%
|
|
JAK1/2/3 Inhibitor 1 is a potent protein kinase inhibitor.JAK1/2/3 Inhibitor 1 has antitumor activity that inhibits the growth of a variety of cancer cell lines....
|
T21674L |
PKA inhibitor fragment (6-22) amide Acetate
|
T21674L
|
99.30%
|
|
PKA inhibitor fragment (6-22) amide Acetate is a synthetic peptide which selectively inhibits PKA activity by binding to its substrate site (IC50 < 2 nM).
|
TP1787L |
PKG Substrate acetate(81187-14-6 free base)
|
TP1787L
|
99.30%
|
|
PKG Substrate acetate is a selective substrate for cGMP-dependent protein kinase (PKG).PKG Substrate is a selective substrate for protein kinase G (PKG) with a s...
|
T1920 |
Capivasertib
|
1143532-39-1
|
99.29%
|
|
Capivasertib (AZD5363) is a broad-spectrum AKT inhibitor with inhibitory activity against Akt1, Akt2, and Akt3 (IC50=3/7/7 nM) with oral activity. Capivasertib h...
|
T6139 |
A-674563
|
552325-73-2
|
99.21%
|
|
A-674563 is an Akt1 inhibitor with Ki of 11 nM, modest potent to PKA and >30-fold selective for Akt1 over PKC.
|
T6303 |
CCT128930
|
885499-61-6
|
99.18%
|
|
CCT128930 is a potent, ATP-competitive and selective inhibitor of Akt2 with IC50 of 6 nM, 28-fold greater selectivity for Akt2 than the closely related PKA kinas...
|
T6315 |
MLN8054
|
869363-13-3
|
99.05%
|
|
MLN8054 is a potent and selective Aurora A kinase inhibitor with an IC50 of 4 nM.
|