EC Number   |
Application |
Reference |
|---|
  1.1.1.422 | industry |
the wide substrate spectrum of these dehydrogenases, combined with their regio- and enantioselectivity, suggests a high potential for the industrial production of valuable chiral compounds |
752351 |
| 1.1.1.422 | more |
both (R,S)-(-)-ephedrine and (S,S)-(+)-pseudoephedrine are constituents of various over-the-counter (OTC) drugs and are also used as decongestants and stimulants. Arthrobacter sp. TS-15 and its isolated ephedrine-oxidizing enzymes have potential for use in decontamination and synthetic applications |
755862 |
| 1.1.1.422 | synthesis |
the enzyme catalyzes the oxidation of an isomers of ephedrine and the regio- and enantioselective reduction of sterically demanding substrate 1-phenyl-1,2-propanedione to give (S)-phenylacetylcarbinol. (S)-phenylacetylcarbinol can serve as a precursor in the synthesis of many pharmaceuticals, such as (+)-(S,S)-pseudoephedrine |
752351 |
| 1.1.1.422 | synthesis |
the wide substrate spectrum of the dehydrogenase, combined with its regio- and enantioselectivity, suggests a high potential for the industrial production of valuable chiral compounds |
752351 |
| 1.1.1.422 | synthesis |
the wide substrate spectrum of these dehydrogenases, combined with their regio- and enantioselectivity, suggests a high potential for the industrial production of valuable chiral compounds |
752351 |
