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SNX-2112

Cat. No. M3528

All AbMole products are for research use only, cannot be used for human consumption.

SNX-2112 Structure
Synonym:

PF-04928473

Size Price Availability Quantity
2mg USD 130 In stock
5mg USD 190 In stock
10mg USD 270 In stock
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Quality Control & Documentation
Biological Activity

SNX-2112 is a potent synthetic heat shock protein 90 inhibitor with an IC50 of 0.92 μM for K562 cells. The heat shock protein 90 (Hsp90) chaperone not only regulates the conformational maturation but also stables the structures of oncogenic kinases as well as transcription factors. SNX-2112 is an active metabolite of the compounds SNX-5542. SNX-2112 is rapidly transformed form SNX-5542 after administration. In a panel of tumor cell lines, SNX-2112 degraded HER2 and mutant epidermal growth factor receptor and inhibited extracellular signal-modulated kinase and Akt activation.SNX-2112 inducen a Rb-dependent G1 arrest with subsequent apoptosis. which accumulates in tumors relative to normal tissues.

Protocol (for reference only)
Cell Experiment
Cell lines BT474, SKBR-3, SKOV-3, MDA-468, MCF-7 and H1650 cancer cells
Preparation method Determining cell viability by seeding 2-5 × 103 cells per well in 96- well plates and treating with SNX-2112 24 hours after plating in complete medium (200 μL). Testing each drug concentration in eight wells. After a 96-h incubation ,using the Alamar blue viability test to assay cells . Flow cytometry is done using nuclei stained with ethidium bromide and isolated via the Nusse protocol
Concentrations 0-500 nM
Incubation time 24 hours
Animal Experiment
Animal models 5 ?106 MM.1S cells are inoculated subcutaneously in the Fox Chase SCID mice (6-7 weeks old).
Formulation SNX-5422 is dissolved in 1% carboxy methylcellulose/0.5% Tween 80 at 10 mg/mL and stored at 4 癈 for in vivo stud
Dosages 20 or 40 mg/kg
Administration SNX-5422 is administered orally 3 times per week, total 3 weeks.
Chemical Information
Molecular Weight 464.48
Formula C23H27F3N4O3
CAS Number 908112-43-6
Solubility (25°C) DMSO 83 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Xiaozhen Cheng, et al. SNX-2112 Induces Apoptosis and Inhibits Proliferation, Invasion, and Migration of Non-Small Cell Lung Cancer by Downregulating Epithelial-Mesenchymal Transition via the Wnt/β-Catenin Signaling Pathway

[2] Chuanchuan Nan, et al. Antitumorigenic Effect of Hsp90 Inhibitor SNX-2112 on Tongue Squamous Cell Carcinoma is Enhanced by Low-Intensity Ultrasound

[3] Liubing Hu, et al. Hsp90 Inhibitor SNX-2112 Enhances TRAIL-Induced Apoptosis of Human Cervical Cancer Cells via the ROS-Mediated JNK-p53-Autophagy-DR5 Pathway

[4] Natsuko Fukuoka, et al. SNX-2112 Induces Apoptosis and Autophagy of Nara-H Cells

[5] Yuting Liu, et al. Combination of SNX-2112 with 5-FU exhibits antagonistic effect in esophageal cancer cells

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  Catalog
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Keywords: SNX-2112, PF-04928473 supplier, HSP, inhibitors, activators

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