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BIO-Acetoxime

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    BIO-Acetoxime
  • BIO-Acetoxime
Cat No: 16329
Biochemicals - Kinase Inhibitors
Cayman

BIO-Acetoxime is an analog of the GSK3 inhibitor 6-bromoindirubin-3’-oxime, or BIO (Item No. 13123).{17160,17161} It potently inhibits GSK3α/β (IC50 = 10 nM), with selectivity over Cdk5/p25, Cdk2/A, and Cdk1/B (IC50s = 2.4, 4.3, and 63 µM, respectivel...

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

Territorial Availability: Available through Bertin Technologies only in France
Synonyms:
  • 3-[3-[(acetyloxy)imino]-1,3-dihydro-2H-indol-2-ylidene]-6-bromo-1,3-dihydro-2H-indol-2-one
Correlated keywords:
  • 667463-85-6 1044661-40-6 1110670-47-7 biochemical inhibitor intracellular signaling antiviral cell biology signal transduction Alzheimer’s research neuroscience GSK3 GSK-3 GSK3α GSK3β acetoxime analog 6-bromoindirubin-3’-oxime inhibit Wnt/β-catenin pathway suppress suppressor cytopathic effect herpes virus reduce viral yield human oral epithelial cells potent selective BIOacetoxime
Product Overview:
BIO-Acetoxime is an analog of the GSK3 inhibitor 6-bromoindirubin-3’-oxime, or BIO (Item No. 13123).{17160,17161} It potently inhibits GSK3α/β (IC50 = 10 nM), with selectivity over Cdk5/p25, Cdk2/A, and Cdk1/B (IC50s = 2.4, 4.3, and 63 µM, respectively).{17160,17161} BIO-Acetoxime has been used to study the role of GSK3 in the Wnt/β-catenin pathway.{27753} It also suppresses the cytopathic effects of herpes viruses and reduces viral yields in human oral epithelial cells.{27754}
Size 1 mg
Shipping dry ice
CAS Number 740841-15-0
Molecular Formula C18H12BrN3O3
SMILES CC(O/N=C(/C(N1)=C2C(NC3=C\2C=CC(Br)=C3)=O)C4=C1C=CC=C4)=O
Molecular Weight 398,2
Formulation A crystalline solid
Purity ≥95%
Custom Code 2933.49
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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