| R2033033 |
LY3177833 |
LY3177833 is a CDC7 and pMCM2 inhibitor with IC50 values of 3.3 nM and 290 nM, r
|
| R2033034 |
NAV2729 |
NAV-2729 is a dual Arf1/Arf6 activation inhibitor.
|
| R2033035 |
Porcupine-IN-1 |
Porcn-IN-1 is potent porcupine inhibitor with an IC50 of 0.5±0.2 nM.
|
| R2033036 |
SB242235 |
SB-242235 is a potent and selective p38 MAP kinase inhibitor, with an IC50 of 1.
|
| R2033037 |
SR9009 |
SR9009 is a REV-ERBα/β agonist with IC50s of 670 nM and 800 nM for REV-ERBα and
|
| R2033038 |
Voruciclib |
Voruciclib is an orally active and selective CDK inhibitor with Ki values of 0.6
|
| R2033039 |
WAY316606 |
WAY 316606 is an inhibitor of the secreted protein sFRP-1, an endogenous antagon
|
| R2033040 |
XAV939 |
XAV-939 is a Wnt/β-catenin pathway inhibitor.XAV-939 stabilizes axin by inhibiti
|
| R2033041 |
CID16020046 |
CID 16020046 is a potent and selective GPR55(LPI receptor) antagonist; inhibitsG
|
| R2033042 |
MF63 |
MF63 is a selective mPGES-1 inhibitor with an IC50 of 0.9 nM and 1.3 nM for pig
|
| R2033043 |
ML240 |
ML240 is a potent p97 inhibitor, inhibiting p97 ATPase with IC50 value of 100 nM
|
| R2033044 |
AG879 |
Tyrphostin AG 879 (AG 879) is a tyrosine kinase inhibitor that inhibits TrKA pho
|
| R2033045 |
BAM15 |
BAM 15 is a novel mitochondrial protonophore uncoupler.
|
| R2033046 |
B-Raf inhibitor 1 dihydrochloride |
B-Raf inhibitor 1 dihydrochloride is a potent Raf kinase inhibitor with Kis of 1
|
| R2033047 |
CP671305 |
CP671305 is a potent, orally active, selective inhibitor of phosphodiesterase-4-
|
| R2033048 |
Flavopiridol |
Flavopiridol (Alvocidib) is a broad spectrum and competitive inhibitor of CDKs,
|
| R2033049 |
GlyT2-IN-1 |
Yoda 1 is a Piezo1 agonist.Yoda 1 activates purified Piezo1 channels.
|
| R2033050 |
GSK189254A |
GSK189254A (GSK189254) is a novel, potent and selective histamine H3 receptor an
|
| R2033051 |
HA-15 |
HA15 is a potent and specific inhibitor of ER chaperone BiP/GRP78/HSPA5, inhibit
|
| R2033052 |
HG-10-102-01 |
HG-10-102-01 is a potent and selective inhibitor of wild-type LRRK2(IC50=23.3 nM
|
| R2033053 |
JQEZ5 |
JQEZ5 is a novel and potent EZH2 inhibitor.
|
| R2033054 |
Lazertinib |
Lazertinib is a potent, highly mutant-selective, blood-brain barrier permeable,
|
| R2033055 |
Mapracorat |
Mapracorat is a novel non-steroidal selective glucocorticoid receptor agonist.
|
| R2033056 |
MAZ51 |
MAZ51 is a selective inhibitor of VEGFR-3 (Flt-4) tyrosine kinase.MAZ51 inhibits
|
| R2033057 |
MBX8025 |
Seladelpar (MBX-8025) is an orally active, potent (50% effect concentration EC50
|