Cat. No. |
Product Name |
Information |
PC-60462 |
SP 141
|
A novel specific MDM2 inhibitor that promotes MDM2 auto-ubiquitination and degradation. |
PC-60443 |
RO-5963
|
A potent, dual MDM2/MDMX-p53 interaction inhibitor with IC50 of 17 and 24 nM, respectively. |
PC-60442 |
AM-8735
|
A potent MDM2-p53 interaction inhibitor with remarkable biochemical (HTRF IC50=0.4 nM), cellular potency (SJSA-1 EdU IC50=25 nM), and favorable pharmacokinetic properties. |
PC-60441 |
AM-8553
|
A potent, selective, orally bioavailable MDM2-p53 interaction inhibitor with HTRF IC50 of 1.1 nM, SJSA-1 EdU IC50 of 68 nM. |
PC-60440 |
AM-6761
|
A potent MDM2-p53 interaction inhibitor with remarkable biochemical (HTRF IC50=0.1 nM), cellular potency (SJSA-1 EdU IC50=16 nM), and favorable pharmacokinetic properties. |
PC-60439 |
TDP-665759
|
A small molecule inhibitor of HDM2-p53 interaction with FP IC50 of 0.7 uM. |
PC-60438 |
NU-8165
|
A small molecule inhibitor of MDM2-p53 protein-protein interaction with IC50 of 16 uM.. |
PC-60437 |
NU-8231
|
A small molecule inhibitor of MDM2-p53 protein-protein interaction with IC50 of 5.3 uM in ELISA assay. |
PC-60436 |
WK-298
|
A potent small molecule inhibitor that binds and disrupts the MDM2/MDMX-p53 interaction with IC50 of 0.19 uM and 19.7 uM, respectively.. |
PC-60304 |
RO-5353
|
A potent, selective, and orally active p53-MDM2 antagonist with IC50 of 7 nM. |
PC-60303 |
RO-2468
|
A potent, selective, and orally active p53-MDM2 antagonist with IC50 of 6 nM. |
PC-60301 |
BI-0252
|
A potent, highly selective, orally active MDM2-p53 interaction inhibitor with IC50 of 4 nM. |