| Cat. No. |
Product Name |
Information |
| PC-42963 |
CFI-400945
PLK4 inhibitor
|
CFI-400945 (Ocifisertib) is a potent, highly selective PLK4 inhibitor with Ki of 0.26 nM and IC50 of 2.8 nM, does not significantly inhibits PLK1/2/3 at 50 uM. |
| PC-42899 |
Volasertib
PLK inhibitor
|
Volasertib (BI 6727) is a potent, selective Polo-like kinase (PLK) inhibitor with IC50 of 0.87, 5 and 56 nM for PLK1, 2 and 3, respectively. |
| PC-42860 |
HMN-214
PLK1 inhibitor
|
HMN-214 (IVX 214, TV-7101) is a prodrug of HMN-176 for oral administration, HMN-176 is a stilbene derivative that interferes with the subcellular spatial location of PLK1, does not inhibit PLK directly. |
| PC-42852 |
Rigosertib
PLK1 inhibitor
|
Rigosertib (ON 01910) is a potent, non-ATP-competitive PLK1 inhibitor (IC50=9-10 nM), selectively induces mitotic G2/M arrest and apoptosis in cancer cells. |
| PC-42851 |
Rigosertib sodium
PLK1 inhibitor
|
Rigosertib sodium (ON 01910.Na) is a potent, non-ATP-competitive PLK1 inhibitor (IC50=9-10 nM), selectively induces mitotic G2/M arrest and apoptosis in cancer cells. |
| PC-63063 |
T-521
PLK1 inhibitor
|
T-521 is a novel PLK1 PBD (Polo-box domain) inhibitor that specifically inhibits the PBD of PLK1 (IC50=1.22 uM), but not those of Plk2-3. |
| PC-62790 |
PLK1-IN-14f
PLK1 inhibitor
|
PLK1-IN-14f is a potent PLK1 inhibitor, exhibits potent activity against a panel cancer cell lines with GI50 values ranging from 0.30 to 0.60 uM. |
| PC-62393 |
Poloxin
PLK1 inhibitor
|
Poloxin is the first reported PLK1 PBD inhibitor with IC50 of 6.4 uM, shows less potent inhibition for Plk2 PBD and Plk3 PBD. |
| PC-62159 |
Cyclapolin 1
PLK1 inhibitor
|
Cyclapolin 1 is a potent and selective PLK1 inhibitor that promotes loss of centrosome integrity and microtubule nucleating ability apparently through increased accessibility of protein phosphatases. |
| PC-62158 |
Cyclapolin 9
PLK1 inhibitor
|
Cyclapolin 9 is a potent, selective, and ATP-competitive polo-like kinase PLK1 inhibitor with IC50 of 500 nM. |
| PC-61201 |
Poloppin II
PLK1 inhibitor
|
Poloppin II is an orally active, Poloppin derivative inhibitor of protein-protein interaction via the PBD of the mitotic Polo-like kinase (PLK) with IC50 of 41 uM in FP assays, exhibits IC50 of 61 nM cellular assay for mitotic arrest. |
| PC-61200 |
Poloppin
PLK1 inhibitor
|
Poloppin is a cell-active, small molecule inhibitor of protein-protein interaction via the Polo-box domain (PBD) of the mitotic Polo-like kinase (PLK) with IC50 of 26.9 uM (PLK1) in FP assays. |
