| R21082280 |
R547 |
R547 is a potent ATP-competitive inhibitor of CDK1/2/4 with Ki of 2 nM/3 nM/1 nM
|
| R21082281 |
YS-49 |
YS-49 is an activator of PI3K/Akt (a downstream target of RhoA).
|
| R21082282 |
YM-90K hydrochloride |
YM90K hydrochloride is an antagonist of AMPA receptor.
|
| R21082283 |
AG-490 |
(E/Z)-AG490 ((E/Z)-Tyrphostin AG490) is a racemate of (E) -Ag490 and (Z) -Ag490.
|
| R21082284 |
D-6413 |
D-64131 is a tubulin polymerization inhibitor that competitively binds to αβ -tu
|
| R21082285 |
KU14R |
KU14R is an insulin receptor antagonist, which can selectively block insulin sec
|
| R21082286 |
Amsilarotene;TAC-101 |
Amsilarotene inhibits the phosphorylation of retinoblastoma gene product (RB) an
|
| R21082287 |
GW7647 |
|
| R21082288 |
LY2623091 |
LY2623091 (LY-2623091) is an oral halocorticoid receptor antagonist for the trea
|
| R21082289 |
SMI-4a |
Tcs-pim-1-4a is a PIM inhibitor that blocks mTORC1 activity through AMPK activat
|
| R21082290 |
LY500307 |
Erteberel (LY500307) is a potent, selective estrogen receptor β (ERβ) inhibitor
|
| R21082291 |
NVP-QAV-572 |
Nav1.7-in-2 is a potent PI3K inhibitor with IC50 of 10 nM. For details, see Exam
|
| R21082292 |
LX1606 |
Telotristat ethyl (LX1606) is an oral tryptophan hydroxylase inhibitor that redu
|
| R21082293 |
Asunaprevir(BMS-650032) |
|
| R21082294 |
AS-252424 |
As252424 is a potent selective PI3Kγ inhibitor with IC50 of 30±10 nM.
|
| R21082296 |
tomeglovir |
Tomeglovir is an anti-CMV agent that inhibits the progression of viral DNA in mu
|
| R21082297 |
OTSSP167 hydrochloride |
OTSSP167 is a potent MELK inhibitor with IC50 value of 0.41 nM.
|
| R21082298 |
K145 hydrochloride |
K145 hydrochloride was a selective inhibitor of SphK2 with IC50 of 4.3μM, and sh
|
| R21082299 |
TH-237A |
Th-237a (MESO-GS 164) is a neuroprotective agent with good blood-brain barrier p
|
| R21082300 |
Deferitrin |
Deferitrin (GT-56-252) is a deferric sulfide (DFT) analogue, which is a trident
|
| R21082301 |
MX1013 |
MX1013 is a dipeptide pan-caspase inhibitor that inhibits caspase-1
|
| R21082302 |
Pardoprunox |
Pardoprunox(SLV-308) is an agonist of dopamine receptors D2, D3, and 5-HT1A, an
|
| R21082303 |
CP465022 hydrochloride |
CP 465022 hydrochloride is a selective GluR (AMPA) antagonist which is non-compe
|
| R21082304 |
JZL-195 |
JZL195 is a highly effective and selective dual inhibitor of FAAH/MAGL, with IC5
|
| R21082305 |
Endoxifen |
Endoxifen Z-isomer, the most important Tamoxifen metabolite, induced anti-estrog
|