| Weight | 118.132 g/mol |
|---|---|
| Formula | C5H10O3 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 3 |
2-Hydroxypentanoic acid (6450-97-1, 617-31-2)
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- Chirospecific Synthesis of (S)-(+)- and (R)-(-)-5-Amino-4-hydroxypentanoic Acid from L- and D-Glutamic Acid via (S)-(+)- and (R)-(-)-5-Hydroxy-2-oxopiperidine (Synthesis, 1986)
- The mechanism of antifungal action of (S)-2-amino-4-oxo-5-hydroxypentanoic acid, RI-331: the inhibition of homoserine dehydrogenase in Saccharomyces cerevisiae. (Biochemical and Biophysical Research Communications, 1990)
- The mode of antifungal action of (S)2-amino-4-oxo-5-hydroxypentanoic acid, RI-331. (The Journal of Antibiotics, 1990)
- MECHANISM OF ACTION OF AN ANTIFUNGAL ANTIBIOTIC, RI-331, (S) 2-AMINO-4-OXO-5-HYDROXYPENTANOIC ACID; KINETICS OF INACTIVATION OF HOMOSERINE DEHYDROGENASE FROM Saccharomyces cerevisiae (The Journal of Antibiotics, 1992)
- Polypeptide derivatives containing 5-amino-2,5-disubstituted-4-hydroxypentanoic acid residues (1986)
- Stereocontrolled synthesis of all four stereoisomers of fully protected 2-amino-3-hydroxypentanoic acid from imines derived from d-glyceraldehyde (Tetrahedron, 1999)
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Predict GHS Hazards for Any Chemical in silico.
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SMILESCCCC(C(=O)O)O
-
InChIKeyJRHWHSJDIILJAT-UHFFFAOYSA-N
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