| Weight | 115.132 g/mol |
|---|---|
| Formula | C5H9NO2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 1 |
L-proline
Proline · L Proline
344-25-2, 4305-67-3, 147-85-3, 37159-97-0
Score:
#236 in Biochemistry
,
#916 in Biology
,
#1011 in Chemistry
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- Rapid determination of free proline for water-stress studies (Plant and Soil, 1973)
- HIF Targeted for VHL-Mediated Destruction by Proline Hydroxylation: Implications for O2 Sensing (Science, 2001)
- Roles of glycine betaine and proline in improving plant abiotic stress resistance (Environmental and Experimental Botany, 2007)
- Proline-Catalyzed Direct Asymmetric Aldol Reactions (Journal of the American Chemical Society, 2000)
- Proline biosynthesis and osmoregulation in plants (Plant Journal, 1993)
- Proline: a multifunctional amino acid (Trends in Plant Science, 2010)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Proline
- L Proline
-
SMILESC1CC(NC1)C(=O)O
-
InChIKeyONIBWKKTOPOVIA-UHFFFAOYSA-N
- Pubchem - L-proline
- Wikipedia - proline
Proline (abbreviated as Pro or P; encoded by the codons CCU, CCC, CCA, and CCG) is an amino acid that is used in the biosynthesis of proteins. It contains an -amino group (which is in the protonated NH2+ form under biological conditions), an -carboxylic acid group (which is in the deprotonated COO form under biological conditions), and a side chain pyrrolidine, classifying it as a nonpolar (at physiological pH), aliphatic amino acid. It is non-essential in humans, meaning the body can synthesize it from the non-essential amino acid L-glutamate.
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