| Weight | 131.131 g/mol |
|---|---|
| Formula | C5H9NO3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 3 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 1 |
4-Hydroxy-L-proline (6912-67-0, 30724-02-8)
Score:
#1530 in Biochemistry
,
#4453 in Chemistry
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- A SELF-DESTROYING POLYCATIONIC POLYMER : BIODEGRADABLE POLY(4-HYDROXY-L-PROLINE ESTER) (Journal of the American Chemical Society, 1999)
- Poly(4-hydroxy-L-proline ester) : Low-temperature polycondensation and plasmid DNA complexation (Macromolecules, 1999)
- Enantioselective arylation of 2-methylacetoacetates catalyzed by CuI/trans-4-hydroxy-L-proline at low reaction temperatures. (Journal of the American Chemical Society, 2006)
- (Phosphinyloxy)acyl amino acid inhibitors of angiotensin converting enzyme (ACE). 1. Discovery of (S)-1-[6-amino-2-[[hydroxy(4-phenylbutyl)phosphinyl]oxy]-1-oxohexyl]-L-proline, a novel orally active inhibitor of ACE (Journal of Medicinal Chemistry, 1988)
- Trans-4-hydroxy-L-proline, a useful and versatile chiral starting block (Tetrahedron, 1996)
- Prevention of Collagen Deposition Following Pulmonary Oxygen Toxicity in the Rat by Cis-4-Hydroxy-l-Proline (Journal of Clinical Investigation, 1980)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1C(CNC1C(=O)O)O
-
InChIKeyPMMYEEVYMWASQN-UHFFFAOYSA-N
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