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Formula | C30H30Cl2N4O4 |
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Molecular Weight | 581.49 | CAS No. | 675576-98-4 | ||||
Solubility (25°C)* | In vitro | DMSO | 100 mg/mL (171.97 mM) | ||||
Ethanol | 100 mg/mL (171.97 mM) | ||||||
Water | Insoluble | ||||||
In vivo (Add solvents to the product individually and in order) |
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* <1 mg/ml means slightly soluble or insoluble. * Please note that Selleck tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations. * Room temperature shipping (Stability testing shows this product can be shipped without any cooling measures.) |
Description | Nutlin-3a ((-)-Nutlin-3), the active enantiomer of Nutlin-3, inhibits the p53/MDM2 interaction with IC50 of 90 nM in a cell-free assay. Nutlin-3a induces autophagy and apoptosis in a p53-dependent manner. | ||
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Targets |
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In vitro | Nutlin-3a displaces p53 from the binding pocket of MDM2 and thereby releases p53 from inhibition and proteasomal degradation, leading to induction of its downstream targets, cell cycle arrest, and apoptosis. Seven days of incubation with 10 μM nutlin-3a led to >90% inhibition of NIH3T3 cells’ growth[1]. Nutlin-3a stabilizes and activates p53, and induces p21 expression in a dose-dependent manner[1]. Nutlin-3a effectively depletes the S-phase compartment to 0.2-2% and increases the G1- and G2/M-phase compartments[1]. Nutlin-3a induces apoptosis in ~60% of SJSA-1 and MHM cells after 40 h, which increased further after 60 h (85% and 65%, respectively) [1]. | ||
In vivo | Nutlin-3a suppresses xenograft growth in a dose-dependent fashion with the highest dose (200 mg/kg) showing a substantial tumor shrinkage [1]. Nutlin-3 is a selective activator of the p53 pathway in vivo and highly efficacious against SJSA-1 osteosarcoma tumors[1]. Tumors with wild-type p53 and mdm2 gene amplification will respond best to therapy with Nutlin-3a. | ||
Features | Highly selective MDM2 inhibitor with a much lower effect on MDMX. Most effective on tumors with wild type p53. |
Kinase Assay:[3] |
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Cell Assay:[2] |
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Animal Study:[1] |
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, , J Cell Mol Med, 2017, 21(12):3435-3444
Data from [Data independently produced by , , Oncogene, 2016, 35(42):5552-5564]
Data from [Data independently produced by , , Int J Cancer. 2019, 144(4):777-787]
Data from [Data independently produced by , , Cancer Lett, 2016, 381(2):370-9]
CEP192 localises mitotic Aurora-A activity by priming its interaction with TPX2 [ EMBO J, 2024, 10.1038/s44318-024-00240-z] | PubMed: 39327527 |
SPOCK2 modulates neuropathic pain by interacting with MT1-MMP to regulate astrocytic MMP-2 activation in rats with chronic constriction injury [ J Neuroinflammation, 2024, 21(1):57] | PubMed: 38388415 |
Development of a customizable mouse backbone spectral flow cytometry panel to delineate immune cell populations in normal and tumor tissues [ Front Immunol, 2024, 15:1374943] | PubMed: 38605953 |
Application of prime editing system to introduce TP53 R248Q hotspot mutation in acute lymphoblastic leukemia cell line [ Cancer Sci, 2024, 10.1111/cas.16162] | PubMed: 38549229 |
Integrated stress response (ISR) activation and apoptosis through HRI kinase by PG3 and other p53 pathway-restoring cancer therapeutics [ Oncotarget, 2024, 15:614-633] | PubMed: 39288289 |
The Strong Activation of p53 Tumor Suppressor Drives the Synthesis of the Enigmatic Isoform of DUSP13 Protein [ Biomedicines, 2024, 12(7)1449] | PubMed: 39062022 |
Integrated drug response prediction models pinpoint repurposed drugs with effectiveness against rhabdomyosarcoma [ PLoS One, 2024, 19(1):e0295629] | PubMed: 38277404 |
A CANCER PERSISTENT DNA REPAIR CIRCUIT DRIVEN BY MDM2, MDM4 (MDMX), AND MUTANT P53 FOR RECRUITMENT OF MDC1 AND 53BP1 TO [ bioRxiv, 2024, 2024.01.20.576487.] | PubMed: 38328189 |
Comparative landscape of genetic dependencies in human and chimpanzee stem cells [ Cell, 2023, 186(14):2977-2994.e23] | PubMed: 37343560 |
Histone H3 lysine 27 crotonylation mediates gene transcriptional repression in chromatin [ Mol Cell, 2023, 83(13):2206-2221.e11] | PubMed: 37311463 |
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SHIPPING AND STORAGE
Selleck products are transported at room temperature. If you receive the product at room temperature, please rest assured, the Selleck Quality Inspection Department has conducted experiments to verify that the normal temperature placement of one month will not affect the biological activity of powder products. After collecting, please store the product according to the requirements described in the datasheet. Most Selleck products are stable under the recommended conditions.
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