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Postion:Product Catalog >Biochemical Engineering>Inhibitors>Apoptosis>Mdm2 inhibitors>Nutlin-3a
Nutlin-3a
  • Nutlin-3a

Nutlin-3a NEW

Price $45 $64 $97
Package 1mg 2mg 5mg
Min. Order:
Supply Ability: 10g
Update Time: 2024-11-18

Product Details

Product Name: Nutlin-3a CAS No.: 675576-98-4
Purity: 99.05% Supply Ability: 10g
Release date: 2024/11/18

Product Introduction

Bioactivity

NameNutlin-3a
DescriptionNutlin-3a is the active enantiomer of Nutlin-3, an MDM2 antagonist that inhibits MDM2-p53 interaction (Ki=90 nM) and activates p53. Nutlin-3a binds preferentially to the p53-binding pocket of MDM2, leading to stabilization of p53 and activation of the p53 pathway. Nutlin-3a has antitumor activity.
Cell ResearchSRB(Only for Reference)
Kinase AssayBiacore studies: Competition assays are performed on a Biacore S51. A Series S Sensor chip CM5 is derivatized for immobilization of a PentaHis antibody for capture of the His-tagged p53. The level of capture is ~ 200 response units (1 response unit corresponds to 1 pg of protein per mm 2). The concentration of MDM2 protein is kept constant at 300 nM. Test compounds are dissolved in DMSO at 10 mM and further diluted to make a concentration series of inhibitor in each MDM2 test sample. The assays are run at 25 °C in running buffer (10 mM Hepes, 0.15 M NaCl, 2% DMSO). MDM2-p53 binding in the presence of inhibitor is calculated as a percentage of binding in the absence of inhibitor and IC50 is calculated using Microsoft Excel
In vitroMETHODS: N1E-115 cells were treated with Ionomycin calcium (0.2-10 μM) for 3-24 h. Cell viability was determined by trypan blue dye exclusion assay. RESULTS: Ionomycin calcium induced cell death in a concentration and time dependent manner. [1] METHODS: Fura-2-loaded mouse cerebellar astrocytes were treated with Ionomycin calcium (0.1-10 μM) for 35 min, and cell membrane Ca(2+) concentration was monitored by changes in the Fura-2 340/380 ratio. RESULTS: At concentrations ≤1 μM [Ca2+]c slowly declined after the initial peak, reaching significantly lower levels after 35 min. However, at 2 μM of ionomycin the peak level of [Ca2+]c was sustained in the plateau phase, and at concentrations >2 μM ionomycin [Ca2+]c was significantly higher after 35 min than at the initial peak. [2]
In vivoMETHODS: To investigate the mechanism of demyelination induced in vivo, Ionomycin calcium (2-50 μM, 0.5 μL) was dorsal column injected into SD rats. RESULTS: Rats injected with Ionomycin calcium showed varying degrees of lesions observed from days 1-21, including areas of localized edema, a small number of scattered demyelinated axons, and larger lesions containing up to 200 demyelinated or degenerated axons. [3]
Storagestore at low temperature,keep away from direct sunlight | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility InformationEthanol : 58.2 mg/mL (100 mM)
DMSO : 55 mg/mL (94.58 mM)
KeywordsE1 activating enzyme | inhibit | E3 ligating enzyme | p53 | carcinomas | E1/E2/E3 Enzyme | ovarian | Nutlin-3 | Ubiquitin ligase | Ubiquitin conjugating enzyme | Ubiquitin activating enzyme | Nutlin 3a | Autophagy | Inhibitor | Nutlin-3a | Nutlin3a | MDM-2/p53 | Rebemadlin | E2 conjugating enzyme | Apoptosis
Inhibitors RelatedStavudine | 5-Fluorouracil | Sodium 4-phenylbutyrate | L-Ascorbic acid | Hydroxychloroquine | Guanidine hydrochloride | Taurine | Tributyrin | Curcumin | Paeonol | Naringin | Gefitinib
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Company Profile Introduction

Target Molecule Corp. (TargetMol) is a global high-tech enterprise, headquartered in Boston, MA, specializing in chemical and biological research product and service to meet the research needs of global customers. TargetMol has evolved into one of the biggest global compound library and small molecule suppliers and a customer based on 40+ countries. TargetMol offers over 80 types of compound libraries and a wide range of high-quality research chemicals including inhibitors, activator, natural compounds, peptides, inhibitory antibodies, and novel life-science kits, for laboratory and scientific use. Besides, virtual screening service is also available for customers who would like to conduct the computer-aided drug discovery.

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