| Weight | 133.147 g/mol |
|---|---|
| Formula | C5H11NO3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 3 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 4 |
2-Amino-5-hydroxypentanoic acid (533-88-0)
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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)
- ChemInform Abstract: 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. (ChemInform, 1986)
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SMILESC(CC(C(=O)O)N)CO
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InChIKeyCZWARROQQFCFJB-UHFFFAOYSA-N
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