|
T11996 |
MELK-8a hydrochloride
|
|
MELK
|
|
|
|
T21559 |
OTSSP167 hydrochloride
|
|
MELK
|
|
OTSSP167 hydrochloride is a highly potent inhibitor of MELK(IC50 : 0.41 nM). |
|
T1759 |
OTSSP167
|
MELK inhibitor,OTS167 |
MELK
|
|
OTSSP167 (OTS167) is an orally available inhibitor of maternal embryonic leucine zipper kinase (MELK) with potential antineoplastic activity. |
|
T11997 |
MELK-IN-1
|
Nintedanib Impurity L,MELK inhibitor 17 |
MELK
|
|
MELK-IN-1 (MELK inhibitor 17) is a potent inhibitor of maternal embryonic leucine zipper kinase (MELK),(IC50:3nm;Ki:0.39 nM). |
|
T24152 |
HTH-01-091
|
HTH-01091,HTH01-091,HTH 01-091,HTH 01091 |
Serine/threonin kinase
,
Pim
,
MELK
,
DYRK
,
CDK
,
RIP kinase
|
|
HTH-01-091 is a potent and selective maternal embryonic leucine zipper kinase (MELK) inhibitor (IC50: 10.5 nM).HTH-01-091 inhibits PIM1/2/3, RIPK2, DYRK3, smMLCK and CLK2. HTH-01-091 can be used to study breast cancer. |
|
T70578 |
BX-795 hydrochloride
|
|
|
|
BX-795 hydrochloride is a TBK1 and IKKε inhibitor. BX-795 is a potential maternal embryonic leucine zipper kinase inhibitor. |
|
T73867 |
HTH-01-091 TFA
|
|
|
|
HTH-01-091 TFA, a potent and selective inhibitor of maternal embryonic leucine zipper kinase (MELK), exhibits an IC50 of 10.5 nM. Besides its primary target, it also inhibits PIM1/2/3, RIPK2, DYRK3, smMLCK, and CLK2, pos... |
