RO8994
Based on 1 Customer Validation
RO8994 (Compound 4) is an orally active, highly potent and selective spiroindolinone p53-MDM2 inhibitor with an IC50 value of 5 nM (HTRF binding assays) and 20 nM (MTT proliferation assays). RO8994 induces up-regulation of p53 expression and Apoptosis in wild-type p53 cancer cells. RO8994 also inhibits tumor growth in the tumor xenograft model.
For research use only. We do not sell to patients.
- Purity: 99.70%
- CAS No.: 1309684-94-3
- Formula: C31H31Cl2FN4O4
- Molecular Weight:613.51
-
Storage:Powder -20°C, 3 years , 4°C, 2 years ; In solvent -80°C, 2 years , -20°C, 1 year
Biological Activity
|
Cell Line
|
Type | Value | Description | References |
|---|---|---|---|---|
| SJSA-1 | IC50 |
0.013 μM
Compound: RO8994
|
Antiproliferative activity against human SJSA cells expressing wild-type p53 by MTT assay
Antiproliferative activity against human SJSA cells expressing wild-type p53 by MTT assay
|
[PMID: 24900784] |
| SW480 | IC50 |
5.19 μM
Compound: RO8994
|
Antiproliferative activity against human SW480 cells expressing p53 mutant by MTT assay
Antiproliferative activity against human SW480 cells expressing p53 mutant by MTT assay
|
[PMID: 24900784] |
RO8994 dose-dependently and non-genotoxically induces p53 stabilization, cell cycle arrest and Apoptosis in tumor cells retainingwt p53[3].
Activity Results for RO8994 in a Biochemical Binding Assay and Human Cancer Cell Proliferation Assays[1][2][3]<
| compd | HTRF IC50 (nM) | SJSA IC50 (μM) | SW480 IC50 (μM) |
| RO8994 | 5 | 0.013 | 5.19 |