Pro

Esters []
Proline acetate

Molecular structure via molpic
Conformer structure via 3Dmol.js
Molecular formula	C5H9NO2[1]
Molecular mass	115.13 g/mol[1]
Predicted LogP	-2.5[1]
Chirality	racemic[2]

Identifiers []
IUPAC name	pyrrolidine-2-carboxylic acid[1]
SMILES	C1CC(NC1)C(=O)O[1]
InChI	InChI=1S/C5H9NO2/c7-5(8)4-2-1-3-6-4/h4,6H,1-3H2,(H,7,8)[1]
InChIKey	ONIBWKKTOPOVIA-UHFFFAOYSA-N[1]

Dosing

Proline

(Redirected from D-Proline)

Proline (also known as Proline DL-form, CCRIS 8602, 2-Pyrrolidinylcarboxylic acid, (+-)-proline, 210-189-3, DL-Proline, H-DL-Pro-OH, D-Pyrrolidine-2-carboxylic acid, 2-Pyrrolidine carboxylic acid or Prolin) is a substance of the amino acid class.

Chemistry

Proline is typically found in the form of its acetate ester.

Stereochemistry

DL-Proline is a racemic mixture of the logical stereoisomers:

Stereoisomers []
D-Proline L-Proline DL-Proline

See also

• Substituted amino acids
• Anodyne

External links

• Proline (Wikipedia)
• Proline / D-Proline / L-Proline (Wikidata)
• Proline / D-Proline / L-Proline (PubChem)
• Proline / D-Proline / L-Proline (ChEMBL)
• Proline / D-Proline / L-Proline (ChEBI)
• Proline / D-Proline / L-Proline (Common Chemistry)
• Proline / D-Proline / L-Proline (HMDB)
• Proline / D-Proline / L-Proline (KEGG)
• Proline / D-Proline / L-Proline (UNII)
• Proline / D-Proline / L-Proline (EPA DSSTox)