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Literature summary for 1.11.1.10 extracted from

  • Masdeu, G.; Perez-Trujillo, M.; Lopez-Santin, J.; Alvaro, G.
    Chloroperoxidase-catalyzed amino alcohol oxidation Substrate specificity and novel strategy for the synthesis of N-Cbz-3-aminopropanal (2016), Process Biochem., 51, 1204-1211 .
No PubMed abstract available

KM Value [mM]

KM Value [mM] KM Value Maximum [mM] Substrate Comment Organism Structure
34
-
N-Cbz-3-amino-1-propanol pH 5.0, 25°C Leptoxyphium fumago

Organism

Organism UniProt Comment Textmining
Leptoxyphium fumago
-
-
-

Source Tissue

Source Tissue Comment Organism Textmining
commercial preparation
-
Leptoxyphium fumago
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
3-amino-1-propanol + H2O2 44% conversion Leptoxyphium fumago 3-aminopropanal + H2O
-
?
3-amino-1-propanol + tert-butyl hydroperoxide 83.6% conversion Leptoxyphium fumago 3-aminopropanal + H2O + ?
-
?
benzyl N-(2-hydroxyethyl)carbamate + H2O2 24.4% conversion Leptoxyphium fumago ? + H2O
-
?
benzyl N-(2-hydroxyethyl)carbamate + H2O2 25.7% conversion Leptoxyphium fumago ? + H2O
-
?
benzyl N-(2-hydroxyethyl)carbamate + tert-butyl hydroperoxide 18.8% conversion Leptoxyphium fumago ? + H2O
-
?
benzyl N-(2-hydroxyethyl)carbamate + tert-butyl hydroperoxide 77.9% conversion Leptoxyphium fumago ? + H2O
-
?
N-Cbz-3-amino-1-propanol + H2O2 9.7% conversion Leptoxyphium fumago N-Cbz-3-aminopropanal + H2O
-
?
N-Cbz-3-amino-1-propanol + tert-butyl hydroperoxide 10.9% conversion Leptoxyphium fumago N-Cbz-3-aminopropanal + H2O + ?
-
?
N-Cbz-5-aminopentanol + H2O2 16.3% conversion Leptoxyphium fumago N-Cbz-5-aminopentanal + H2O
-
?
N-Cbz-5-aminopentanol + tert-butyl hydroperoxide 16.8% conversion Leptoxyphium fumago N-Cbz-5-aminopentanal + H2O + ?
-
?
N-Cbz-6-aminohexanol + H2O2 12.3% conversion Leptoxyphium fumago N-Cbz-6-aminohexanal + H2O
-
?
N-Cbz-6-aminohexanol + tert-butyl hydroperoxide 9.4% conversion Leptoxyphium fumago N-Cbz-6-aminohexanal + H2O + ?
-
?