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Literature summary extracted from
- Enzymatic transformations. Part 55: Highly productive epoxide hydrolase catalyzed resolution of an azole antifungal key synthon (2004), Tetrahedron, 60, 601-605.
No PubMed abstract available
Organism
| EC Number | Organism | UniProt | Comment | Textmining |
|---|---|---|---|---|
| 3.3.2.10 | Aspergillus niger | - |
- |
- |
Source Tissue
| EC Number | Source Tissue | Comment | Organism | Textmining |
|---|---|---|---|---|
| 3.3.2.10 | commercial preparation | - |
Aspergillus niger | - |
Substrates and Products (Substrate)
| EC Number | Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
|---|---|---|---|---|---|---|---|
| 3.3.2.10 | (R)-1-chloro-2-(2,4-difluorophenyl)-2,3-epoxypropane + H2O | in a racemic mixture only the (R)-enantiomeric epoxide is converted to the (R)-enantiomeric diol | Aspergillus niger | (R)-3-chloro-2-(2,4-difluoro-phenyl)-propane-1,2-diol | - |
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Release 2023.1 (January 2023)
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