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Results 1 - 10 of 10
EC Number Application Commentary Reference
Display the word mapDisplay the reaction diagram Show all sequences 4.1.2.42medicine efficient biocatalyst for resolution of L-X-3,4-methylenedioxyphenylserine, an intermediate for production of a therapeutic drug for Parkinson's disease 649398
Display the word mapDisplay the reaction diagram Show all sequences 4.1.2.42medicine low-specificity threonine aldolase can be used in production of L-threo-3-[4-(methylthio)phenylserine], an intermediate for synthesis of antibiotics florfenicol and thiamphenicol -, 649393
Display the word mapDisplay the reaction diagram Show all sequences 4.1.2.42pharmacology efficient, environmentally friendly process for the production of (2R,3S)-2-amino-3-hydroxy-3-(pyridin-4-yl)-propanoic acid by a recombinant D-threonine aldolase catalyzed aldol addition of glycine and pyridine 4-carboxaldehyde. (2R,3S)-2-amino-3-hydroxy-3-(pyridin-4-yl)-propanoic acid, is a key intermediate in the synthesis of the (2R,3S)-2-amino-3-hydroxy-3-(pyridin-4-yl)-1-(pyrrolidin-1-yl)propan-1-one, a developmental drug candidate. The aldol addition product directly crystallizes out from the reaction mixture in high purity and high diastereo- and enantioselectivity, contributing to high yield and allowing easy isolation, processing, and downstream utilization -, 748821
Display the word mapDisplay the reaction diagram Show all sequences 4.1.2.42pharmacology the enzyme has a considerable potential in biocatalysis for the stereospecific synthesis of various beta-hydroxy amino acids, which are valuable building blocks for the production of pharmaceuticals 749053
Display the word mapDisplay the reaction diagram Show all sequences 4.1.2.42synthesis alanine racemase with engineered function of D-threonine aldolase, capable of synthesizing beta-hydroxy-alpha-amino acids, stereoselectivity is comparable to that of D-threonine aldolase 691309
Display the word mapDisplay the reaction diagram Show all sequences 4.1.2.42synthesis efficient, environmentally friendly process for the production of (2R,3S)-2-amino-3-hydroxy-3-(pyridin-4-yl)-propanoic acid by a recombinant D-threonine aldolase catalyzed aldol addition of glycine and pyridine 4-carboxaldehyde. (2R,3S)-2-amino-3-hydroxy-3-(pyridin-4-yl)-propanoic acid, is a key intermediate in the synthesis of the (2R,3S)-2-amino-3-hydroxy-3-(pyridin-4-yl)-1-(pyrrolidin-1-yl)propan-1-one, a developmental drug candidate. The aldol addition product directly crystallizes out from the reaction mixture in high purity and high diastereo- and enantioselectivity, contributing to high yield and allowing easy isolation, processing, and downstream utilization -, 748821
Display the word mapDisplay the reaction diagram Show all sequences 4.1.2.42synthesis the enzyme can be used for the asymmetric synthesis alpha-quaternary alpha-amino acids 747561
Display the word mapDisplay the reaction diagram Show all sequences 4.1.2.42synthesis the enzyme has a considerable potential in biocatalysis for the stereospecific synthesis of various beta-hydroxy amino acids, which are valuable building blocks for the production of pharmaceuticals 749053
Display the word mapDisplay the reaction diagram Show all sequences 4.1.2.42synthesis the enzyme is a powerful tool for the stereospecific synthesis of various beta-hydroxy amino acids in synthetic organic chemistry 748886
Display the word mapDisplay the reaction diagram Show all sequences 4.1.2.42synthesis the enzyme might be a promising biocatalyst for producing chiral aromatic beta-hydroxy-alpha-amino acids -, 747468
Results 1 - 10 of 10