Nrf2 (C-Term) Polyclonal Antibody
Nrf2 (C-Term) Polyclonal Antibody
Nuclear factor erythroid 2-related factor 2 (Nrf2) is a basic leucine zipper transcription factor encoded by NFE2L2 in humans that...
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€54.00 €45.90
VLX1570 is an inhibitor of 19S proteasomal deubiquitinases with IC50 values of 6.4 and 13 ?M for deubiquitinase activity in vitro using Ub-rhodamine and Ub-AMC, respectively, as substrates.{53378,53379} It is selective for proteasomal deubiquitinases over a panel of deubiquitinases at 20 ?M, but inhibits USP5 by greater than 50%, and over a panel of 211 kinases at 10 ?M, but inhibits Cdk4 by 77%.{53378} VLX1570 binds to and inhibits recombinant ubiquitin-specific protease 14 (USP14) and ubiquitin carboxyl-terminal hydrolase isozyme L5 (UCHL5) in vitro, and inhibits the USP14 and UCHL5 activity of purified 19S proteasomes when used at a concentration of 50 ?M.{53378,53379} It inhibits the proliferation of KMS-11, RPMI-8226, OPM-2, and OPM-2-BZR multiple myeloma cells (IC50s = 43, 74, 126, and 191 nM, respectively), as well as induces apoptosis and increases the accumulation of polyubiquitinated proteins.{53379} VLX1570 (3 mg/kg per day for 10 days) increases survival and reduces tumor growth in KMS-11-LUC2 and RPMI-8226 mouse xenograft models, respectively.
Territorial Availability: Available through Bertin Technologies only in France
| Size | 1 mg, 10 mg, 25 mg, 5 mg |
|---|---|
| Shipping | dry ice |
| CAS number | 1431280-51-1 |
| Molecular formula | C23H17F2N3O6 |
| Smiles | O=C(/C(CCN(C(C=C)=O)C/1)=C/C2=CC([N+]([O-])=O)=C(F)C=C2)C1=CC3=CC=C(F)C([N+]([O-])=O)=C3, O=C(/C(CCN(C(C=C)=O)C/1)=C/C2=CC([N+]([O-])=O)=C(F)C=C2)C1=CC3=CC=C(F)C([N+]([O-])=O)=C3, O=C(/C(CCN(C(C=C)=O)C/1)=C/C2=CC([N+]([O-])=O)=C(F)C=C2)C1=CC3=CC=C(F)C([N+]([O-])=O)=C3, O=C(/C(CCN(C(C=C)=O)C/1)=C/C2=CC([N+]([O-])=O)=C(F)C=C2)C1=CC3=CC=C(F)C([N+]([O-])=O)=C3 |
| Molecular weight | 469,4 |
| Custom code | 2924.29 |
| Formulation | A crystalline solid |
| Purity | ≥98% |
| UNSPSC code | 12352100 |
Cayman Chemical’s mission is to help make research possible by supplying scientists worldwide with the basic research tools necessary for advancing human and animal health. Our utmost commitment to healthcare researchers is to offer the highest quality products with an affordable pricing policy.
Our scientists are experts in the synthesis, purification, and characterization of biochemicals ranging from small drug-like heterocycles to complex biolipids, fatty acids, and many others. We are also highly skilled in all aspects of assay and antibody development, protein expression, crystallization, and structure determination.
Over the past thirty years, Cayman developed a deep knowledge base in lipid biochemistry, including research involving the arachidonic acid cascade, inositol phosphates, and cannabinoids. This knowledge enabled the production of reagents of exceptional quality for cancer, oxidative injury, epigenetics, neuroscience, inflammation, metabolism, and many additional lines of research.
Our organic and analytical chemists specialize in the rapid development of manufacturing processes and analytical methods to carry out clinical and commercial GMP-API production. Pre-clinical drug discovery efforts are currently underway in the areas of bone restoration and repair, muscular dystrophy, oncology, and inflammation. A separate group of Ph.D.-level scientists are dedicated to offering Hit-to-Lead Discovery and Profiling Services for epigenetic targets. Our knowledgeable chemists can be contracted to perform complete sample analysis for analytes measured by the majority of our assays. We also offer a wide range of analytical services using LC-MS/MS, HPLC, GC, and many other techniques.
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ISO/IEC 17025:2005
ISO Guide 34:2009
Cayman is a leader in the field of emerging drugs of abuse, providing high-purity Schedule I-V Controlled Substances to federally-licensed laboratories and qualified academic research institutions for forensic analyses. We are certified by ACLASS Accreditation Services with dual accreditation to ISO/IEC 17025:2005 and ISO Guide 34:2009.
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