Territorial Availability: Available through Bertin Technologies only in France
- Synonyms
- O-2-(acetylamino)-2-deoxy-?-D-glucopyranosyl-(1?4)-O-2-(acetylamino)-2-deoxy-?-D-glucopyranosyl-(1?4)-O-2-(acetylamino)-2-deoxy-?-D-glucopyranosyl-(1?4)-O-2-(acetylamino)-2-deoxy-?-D-glucopyranosyl-(1?4)-2-(acetylamino)-2-deoxy-D-glucose
- Correlated keywords
- 123815-?07-?6 252990-?16-?2 883747-?01-?1 natural products plants biology signals signaling transduction penta N acetylchitopentaose N-acetylchitopentaose chito-oligosaccharides chito oligosaccharides roots nodulations nodules Nods proteins pentameric NodC C NodL L bacteria bacterial lectins cells divisions divides cortex chitin chitosan inhibits inhibitors inhibitions nitric oxides pentaacetyl pentaacetyl-chitopentaose N,N’,N”,N”’,N””-pentaacetylchitinpentaose N,N’,N’’,N’’’,N’’’’-pentaacetyl chitopentaose N,N’,N”,N”’,N””-pentaacetyl-chitopentaose
- Product Overview:
Root nodules, like those induced on the roots of leguminous plants by Rhizobium bacteria, are important sites for the conversion of atmospheric nitrogen into ammonia. The initiation and development of these growths are driven by a variety of nodulation (Nod) proteins produced by the infecting bacteria. Penta-N-acetylchitopentaose is a pentameric chito-oligosaccharide involved in nodulation. It can be produced by NodC, a chito-oligosaccharide synthase, and serve as a substrate for NodL, an O-acetyltransferase.{26339,26337,26334} This bacterial product binds plant root lectins, and this interaction may be important in the promotion of cell division in the root cortex.{26333,26336} Penta-N-acetylchitopentaose, as well as chitin and chitosan, inhibits nitric oxide production in LPS-activated RAW 264.7 macrophages.{26338}
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.