R2032804 |
MLN-120B |
MLN120B is a specific, ATP competitive IKKβ inhibitor with an IC50 of 60 nM.
|
R2032805 |
PX-12 |
PX-12(IV-2) is an irreversible inhibitor of Thioredoxin-1 (Trx-1); inhibits the
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R2032806 |
SecinH3 |
SecinH3 is an antagonist of cytohesins with IC50s of 5.4 μM, 2.4 μM, 5.4 μM, 5.6
|
R2032807 |
SF1670 |
SF1670 is a potent and specific phosphatase and tensin homolog deleted on chromo
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R2032808 |
Sipoglitazar |
NA.
|
R2032809 |
SKI II |
SKI-II is an oral active and synthetic inhibitor of sphingosine kinase (SK) acti
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R2032810 |
SR3029 |
SR-3029 is a potent and ATP competitive CK1δ and CK1ε inhibitor, with IC50s of 4
|
R2032811 |
TAK715 |
TAK-715 is a p38 MAPK inhibitor for p38α with IC50 of 7.1 nM, 28-fold more selec
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R2032812 |
A484954 |
A-484954 is a highly selective eukaryotic elongationfactor-2 (eEF2) inhibitor, w
|
R2032813 |
AMG-458 |
AMG 458 is a potent c-Met inhibitor with Ki of 1.2 nM, ~350-fold selectivity for
|
R2032814 |
AR-13324 hydrochloride;Netarsudil hydrochloride |
Netarsudil hydrochloride (AR-13324 hydrochloride) is a ROCK, and norepinephrine
|
R2032815 |
CP724714 |
CP-724714 is a potent, selective inhibitor of HER2/ErbB2 with IC50 of 10 nM, >
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R2032816 |
Crolibulin |
Crolibulin is a small molecule tubulin polymerization inhibitor.
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R2032817 |
CZ415 |
CZ415 is a potent and highly selective mTOR inhibitor with a pIC50 of 8.07.CZ415
|
R2032818 |
GRT6005 |
Cebranopadol is an analgesic NOP and opioid receptor agonist with Kis/EC50s of 0
|
R2032819 |
GW4869 |
GW4869 is a noncompetitive neutral sphingomyelinase (N-SMase) inhibitor (exosome
|
R2032820 |
IWP-4 |
IWP-4 is a small molecule Wnt inhibitor with an IC50 of 25 nM.
|
R2032821 |
Melinamide |
Melinamide, an amide derivative of an unsaturated long-chain fatty acid, is an i
|
R2032822 |
ML-7 hydrochloride |
ML-7 hydrochloride is a naphthalene sulphonamide derivative, potently inhibits M
|
R2032823 |
Reparixin |
Reparixin is a non-competitive allosteric inhibitor of the chemokine receptors C
|
R2032824 |
STO-609 acetate |
STO-609 is a selective and cell-permeable inhibitor of the Ca2+/calmodulin-depen
|
R2032825 |
TUG891 |
TUG-891is a potent and selective agonist for the long chain free fatty acid (LCF
|
R2032826 |
UNC569 |
UNC569 is a novel small-molecule MER inhibitor with efficacy against acute lymph
|
R2032827 |
APS-2-79 |
APS-2-79 hydrochloride behaves as a kinase suppressor of Ras (KSR)-dependent ant
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R2032828 |
BAY-1082439 |
BAY1082439 is an orally bioavailable inhibitor of the class I phosphoinositide 3
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