Pyroglutamic acid

Pyroglutamic acid
Identifiers
Abbreviations Glp
CAS number 98-79-3 (2S) Y, 4042-36-8 (2R), 149-87-1 N
PubChem 7405 (2S), 439685 (2R), 499, 10534703 (2S)(3,4-3H2)
ChemSpider 7127 (2S) Y, 388752 (2R) Y, 485 Y, 8710094 (2S)(3,4-3H2) Y
UNII SZB83O1W42 Y
EC number 205-748-3
DrugBank DB03088
KEGG C02237 N
MeSH Pyrrolidonecarboxylic+acid
ChEBI CHEBI:16010 N
ChEMBL CHEMBL284718 N
RTECS number TW3710000
Beilstein Reference 82134
Gmelin Reference 1473408
3DMet B01549
Jmol-3D images Image 1
Properties
Molecular formula C5H7NO3
Molar mass 129.11 g mol−1
Exact mass 129.042593095 g mol-1
Melting point

184 °C, 457 K, 363 °F

log P -0.89
Acidity (pKa) -1.76, 3.48, 12.76
Basicity (pKb) 15.76, 10.52, 1.24
Isoelectric point 0.94
 N (verify) (what is: Y/N?)
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa)
Infobox references

Pyroglutamic acid (also known as 5-oxoproline, pidolic acid, or pyroglutamate for its basic form) is an uncommon amino acid derivative in which the free amino group of glutamic acid cyclizes to form a lactam. It is found in many proteins including bacteriorhodopsin. N-terminal glutamine residues can spontaneously cyclize to become pyroglutamate. This is one of several forms of blocked N-terminals which present a problem for N-terminal sequencing using Edman chemistry, which requires a free primary amino group not present in pyroglutamic acid. The enzyme pyroglutamate aminopeptidase can restore a free N-terminus by cleaving off the pyroglutamate residue.[1]

Pyroglutamic acid is also known as pidolic acid, exists as two distinct isomers:

Uses

The sodium salt of pyroglutamic acid – known either as sodium pyroglutamate or sodium pidolate – is used on the skin to retain moisture.

Pyroglutamic acid is sold as a dietary supplement in the United States.

References

  1. ^ Podell, David N.; Abraham, George N. (1978), "A technique for the removal of pyroglutamic acid from the amino terminus of proteins using calf liver pyroglutamate amino peptidase", Biochem. Biophys. Res. Commun. 81 (1): 176–85, doi:10.1016/0006-291X(78)91646-7, PMID 26343 .