n-octyl-beta-valienamine and aniline

n-octyl-beta-valienamine has been researched along with aniline* in 1 studies

Other Studies

1 other study(ies) available for n-octyl-beta-valienamine and aniline

Article	Year
Transformation of quercitols into 4-methylenecyclohex-5-ene-1,2,3-triol derivatives, precursors for the chemical chaperones N-octyl-4-epi-β-valienamine (NOEV) and N-octyl-β-valienamine (NOV). Bioorganic & medicinal chemistry letters, 2011, Dec-01, Volume: 21, Issue:23 (+)-proto-Quercitol (1) and (-)-vibo-quercitol (2), both of which could be readily prepared by the bioconversion of myo-inositol, were successfully converted into the corresponding 4-methylenecyclohex-5-ene-1,2,3-triol derivatives. These compounds were demonstrated to be suitable precursors, preserving their configurations, for bioactive carba-aminosugars such as the potent chemical chaperone drug candidates, N-octyl-4-epi-β-valienamine (NOEV, 3) and N-octyl-β-valienamine (NOV, 4). Topics: Aniline Compounds; Animals; Carbohydrate Sequence; Cattle; Cyclohexanes; Ecdysone; Enzyme Inhibitors; Hexosamines; Inhibitory Concentration 50; Inositol; Liver; Methylene Chloride; Molecular Sequence Data; Structure-Activity Relationship	2011

Article

Year

Transformation of quercitols into 4-methylenecyclohex-5-ene-1,2,3-triol derivatives, precursors for the chemical chaperones N-octyl-4-epi-β-valienamine (NOEV) and N-octyl-β-valienamine (NOV).

Bioorganic & medicinal chemistry letters, 2011, Dec-01, Volume: 21, Issue:23

(+)-proto-Quercitol (1) and (-)-vibo-quercitol (2), both of which could be readily prepared by the bioconversion of myo-inositol, were successfully converted into the corresponding 4-methylenecyclohex-5-ene-1,2,3-triol derivatives. These compounds were demonstrated to be suitable precursors, preserving their configurations, for bioactive carba-aminosugars such as the potent chemical chaperone drug candidates, N-octyl-4-epi-β-valienamine (NOEV, 3) and N-octyl-β-valienamine (NOV, 4).

Topics: Aniline Compounds; Animals; Carbohydrate Sequence; Cattle; Cyclohexanes; Ecdysone; Enzyme Inhibitors; Hexosamines; Inhibitory Concentration 50; Inositol; Liver; Methylene Chloride; Molecular Sequence Data; Structure-Activity Relationship

2011