trans-3'-Benzoyloxy Cotinine 2,3,4-Tri-O-acetyl-N-β-D-glucuronide Methyl Ester Bromide

• Catalog number
  B208175
• Price
  Please ask
• Size
  1 mg

• Chemical available in other sizes
  Please inquire size and price
• Stock availability
  Pending QC
• Cas number
  146490-58-6
• Chemical s molecular weight
  693.49
• Chemical s main applications
  Used in the preparation of Cotinine derivatives, metabolites of Nicotine in humans.
• Chemical s category
  Glucuronides, Heterocycles, Metabolites & Impurities, Mutagenesis Research Chemicals
• Other name
  (2S-trans)-3-[4-(Benzoyloxy)-1-methyl-5-oxo-2-pyrrolidinyl]-1-(2,3,4-tri-O-acetyl-6-methyl-β-D-glucopyranuronosyl)-pyridinium Bromide
• Chemical s formula
  C30H33BrN2O12
• Physical properties
  Beige Solid
• Melting temperature
  No Data Available
• Boiling temperature
  No Data Available
• Chemical s soluble in
  Methanol
• Stability conditions
  No Data Available
• Storage
  No Data Available
• Chemical s specifications
• Description
  N terminal acetylation or CH3CO as epigenetic regulation of trans-3'-Benzoyloxy Cotinine 2 3 4-Tri-O- -N-β-D-glucuronide Methyl Ester Bromide by NATs. A methyl group is an alkyl derived from methane, containing one carbon atom bonded to three hydrogen atoms — CH3. In formulas, the group is often abbreviated Me. Such hydrocarbon groups occur in many organic compounds. It is a very stable group in most molecules. While the methyl group is usually part of a larger molecule, it can be found on its own in any of three forms anion, cation or radical. The anion has eight valence electrons, the radical seven and the cation six. All three forms are highly reactive and rarely observed,

• Gene target
  trans-3   Benzoyloxy   Cotinine   4-Tri-O   N-β-D-glucuronide   Methyl   Ester   Bromide  
• Short name
  trans-3'-Benzoyloxy Cotinine 2 3 4-Tri-O- -N-β-D-glucuronide Methyl Ester Bromide
• Alternative name
  trans-3'-Benzoyloxy Cotinine 2,3,4-Tri-O-acetyl-N-β-D-glucuronide Methyl Ester Bromide

MeSH Data

• Name
  Cloning, Molecular
• Concept
  Scope note: The insertion of recombinant DNA molecules from prokaryotic and/or eukaryotic sources into a replicating vehicle, such as a plasmid or virus vector, and the introduction of the resultant hybrid molecules into recipient cells without altering the viability of those cells.
• Tree numbers
  • E05.393.220
• Qualifiers
  drug effects, methods, radiation effects

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