| Weight | 118.132 g/mol |
|---|---|
| Formula | C5H10O3 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 3 |
4-Hydroxyisovalerate (77220-86-1)
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- SanM catalyzes the formation of 4-pyridyl-2-oxo-4-hydroxyisovalerate in nikkomycin biosynthesis by interacting with SanN. (Biochemical and Biophysical Research Communications, 2007)
- Stereochemical course of the conversion of -ketoisocaproate to -hydroxyisovalerate by soluble, recombinant mammalian 4-hydroxyphenylpyruvate dioxygenase (Tetrahedron, 1997)
- Stereochemistry of hydroxylation during the conversion of -ketoisocaproate to -hydroxyisovalerate by 4-hydroxyphenylpyruvate dioxygenase (Bioorganic & Medicinal Chemistry Letters, 1996)
- ChemInform Abstract: Stereochemistry of Hydroxylation During the Conversion of Ketoisocaproate to Hydroxyisovalerate by 4 Hydroxyphenylpyruvate Dioxygenase. (ChemInform, 2010)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC(CC(=O)O)CO
-
InChIKeyZGYGEPZZMAXSKH-UHFFFAOYSA-N
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