Proline
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| Names | |||
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| IUPAC name
Proline | |||
| Systematic IUPAC name
Pyrrolidine-2-carboxylic acid | |||
| Identifiers | |||
3D model (JSmol) |
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| 80812 | |||
| ChEBI |
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| ChEMBL |
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| ChemSpider | |||
| DrugBank |
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| ECHA InfoCard | 100.009.264 | ||
| EC Number |
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| 26927 | |||
| KEGG |
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| MeSH | Proline | ||
PubChem CID |
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| RTECS number |
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| UNII |
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CompTox Dashboard (EPA) |
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| Properties | |||
| C5H9NO2 | |||
| Molar mass | 115.132 g·mol−1 | ||
| Appearance | Transparent crystals | ||
| Melting point | 205 to 228 °C (401 to 442 °F; 478 to 501 K) (decomposes) | ||
| Solubility | 1.5g/100g ethanol 19 degC | ||
| log P | −0.06 | ||
| Acidity (pKa) | 1.99 (carboxyl), 10.96 (amino) | ||
| Supplementary data page | |||
| Proline (data page) | |||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references | |||
Proline (symbol Pro or P) is an organic acid classed as a proteinogenic amino acid (used in the biosynthesis of proteins), although it does not contain the amino group -NH
2 but is rather a secondary amine. The secondary amine nitrogen is in the protonated form (NH2+) under biological conditions, while the carboxyl group is in the deprotonated −COO− form. The "side chain" from the α carbon connects to the nitrogen forming a pyrrolidine loop, classifying it as a aliphatic amino acid. It is non-essential in humans, meaning the body can synthesize it from the non-essential amino acid L-glutamate. It is encoded by all the codons starting with CC (CCU, CCC, CCA, and CCG).
Proline is the only proteinogenic amino acid which is a secondary amine, as the nitrogen atom is attached both to the α-carbon and to a chain of three carbons that together form a five-membered ring.