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Submit ReviewNutlin 3a is an MDM2 antagonist (IC50 = 90 nM); inhibits the MDM2-p53 interaction. Active enantiomer of Nutlin-3 (Cat. No. 3984). Induces expression for P53 regulated genes. Suppresses tumor growth in vivo >98% in prostate cancer and osteosarcoma cancer models. Antiproliferative.
Nutlin 3a is also offered as part of the Tocriscreen 2.0 Max and Tocriscreen Epigenetics Library. 了解 Tocris 化合物库的更多信息。
分子量 | 581.49 |
公式 | C30H30Cl2N4O4 |
储存 | Store at -20°C |
纯度 | ≥97% (HPLC) |
CAS Number | 675576-98-4 |
PubChem ID | 11433190 |
InChI Key | BDUHCSBCVGXTJM-WUFINQPMSA-N |
Smiles | ClC1=CC=C([C@H]2[C@H](N(C(N3CC(NCC3)=O)=O)C(C4=CC=C(OC)C=C4OC(C)C)=N2)C5=CC=C(Cl)C=C5)C=C1 |
上方提供的技术数据仅供参考。批次相关数据请参见分析证书。
Tocris products are intended for laboratory research use only, unless stated otherwise.
溶剂 | 最高浓度 mg/mL | 最高浓度 mM | |
---|---|---|---|
溶解性 | |||
DMSO | 58.15 | 100 | |
ethanol | 58.15 | 100 |
以下数据基于产品分子量 581.49。 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.
浓度/溶剂体积/质量 | 1 mg | 5 mg | 10 mg |
---|---|---|---|
1 mM | 1.72 mL | 8.6 mL | 17.2 mL |
5 mM | 0.34 mL | 1.72 mL | 3.44 mL |
10 mM | 0.17 mL | 0.86 mL | 1.72 mL |
50 mM | 0.03 mL | 0.17 mL | 0.34 mL |
参考文献是支持产品生物活性的出版物。
Tovar et al (2006) Small-molecule MDM2 antagonists reveal aberrant p53 signaling in cancer: implications for therapy. Proc.Natl.Acad.Sci.USA. 103 1888 PMID: 16443686
Vassilev et al (2004) In vivo activation of the p53 pathway by small-molecule antagonists of MDM2. Science 303 844 PMID: 14704432
If you know of a relevant reference for Nutlin 3a, please let us know.
关键词: Nutlin 3a, Nutlin 3a supplier, Nutlin3a, p53, activators, MDM2, antagonism, antagonists, p53-MDM2, activates, Ubiquitin, E3, Ligases, 6075, Tocris Bioscience
引用文献是使用了 Tocris 产品的出版物。 Nutlin 3a 的部分引用包括:
Slobodan et al (2020) Embryonic Barcoding of Equipotent Mammary Progenitors Functionally Identifies Breast Cancer Drivers. Cell Stem Cell 26 403-419.e4 PMID: 32059806
Catherine et al (2021) p53 mitigates the effects of oncogenic HRAS in urothelial cells via the repression of MCOLN1. iScience 24 102701 PMID: 34222845
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Tocris offers the following scientific literature in this area to showcase our products. We invite you to request* your copy today!
*请注意,Tocris 仅会向正规科研企业/机构地址发送文献。
This brochure highlights the tools and services available from Bio-Techne to support your Targeted Protein Degradation and Induced Proximity research, including:
There are two currently recognized forms of programmed cell death: apoptosis and necroptosis. This poster summarizes the signaling pathways involved in apoptosis, necroptosis and cell survival following death receptor activation, and highlights the influence of the molecular switch, cFLIP, on cell fate.
Degraders (e.g. PROTACs) are bifunctional small molecules, that harness the Ubiquitin Proteasome System (UPS) to selectively degrade target proteins within cells. They consist of three covalently linked components: an E3 ubiquitin ligase ligand, a linker and a ligand for the target protein of interest. Authored in-house, this poster outlines the generation of a toolbox of building blocks for the development of Degraders. The characteristics and selection of each of these components are discussed. Presented at EFMC 2018, Ljubljana, Slovenia