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C646

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    C646
  • C646
Cat No: 10549
Biochemicals - Small Molecule Inhibitors
Cayman
€48.00
Price is excluding VAT and does not include packaging neither shipping

C646 is an inhibitor of the histone acetyltransferase p300 (IC50 = 1.6 μM).{18217} It competitively (versus acetyl-CoA) binds p300 (Ki = 400 nM) and does not inhibit several other acetyltransferases.{18217} The action of C646 appears to be irreversibl...

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This product can only be bought through Cayman Chemical. Please contact us.

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Territorial Availability: Available through Bertin Technologies only in Europe
Synonyms:
  • 4-[4-[[5-(4,5-dimethyl-2-nitrophenyl)-2-furanyl]methylene]-4,5-dihydro-3-methyl-5-oxo-1H-pyra-zol-1-yl]-benzoic acid
Correlated keywords:
  • cancers acetyltransferases chromatin research inhibitors inhibits inhibitions histones modifications genes regulations epigenetics histones modifications acetylation regulations acetyltransferases C-646 C 646 inhibitors inhibits inhibitions p300 p-300 blocks melanoma leukemia lungs prostates cells in vitro memory
Product Overview:
C646 is an inhibitor of the histone acetyltransferase p300 (IC50 = 1.6 μM).{18217} It competitively (versus acetyl-CoA) binds p300 (Ki = 400 nM) and does not inhibit several other acetyltransferases.{18217} The action of C646 appears to be irreversible through covalent modification of the enzyme target.{18217} It blocks the growth of human melanoma, leukemia, lung, and prostate cancer cells in vitro.{18217,22225,22222} C646 has been used to study the role of p300-mediated acetylation in such models as fear extinction memory and the regulation of immediate-early genes.{22223,22224}
Size 1 mg
Shipping dry ice
Stability Store at -20 degrees; shelf life 730 days
CAS Number 328968-36-1
Molecular Formula C24H19N3O6
SMILES CC(C=C1[N+]([O-])=O)=C(C)C=C1C2=CC=C(/C=C3C(C)=NN(C4=CC=C(C(O)=O)C=C4)C/3=O)O2
Molecular Weight 445,4
Formulation A crystalline solid
Purity ≥98% (mixture of isomers)
Custom Code 2916.39
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.

Accreditations
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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