| Identification | Back Directory | [Name]
H-SER-PRO-OH | [CAS]
23827-93-2 | [Synonyms]
Ser-Pro-OH
H-SER-PRO-OH
1-Serylproline
L-Ser-L-Pro-OH
L-SERYL-L-PROLINE
L-Proline, L-seryl-
1-(L-Seryl)-L-proline
(S)-1-((S)-2-Amino-3-hydroxypropanoyl)pyrrolidine-2-carboxylic acid | [Molecular Formula]
C8H14N2O4 | [MDL Number]
MFCD00037333 | [MOL File]
23827-93-2.mol | [Molecular Weight]
202.21 |
| Chemical Properties | Back Directory | [Boiling point ]
524.0±50.0 °C(Predicted) | [density ]
1.430±0.06 g/cm3(Predicted) | [storage temp. ]
-15°C
| [pka]
3.08±0.20(Predicted) | [Sequence]
Ser-Pro |
| Hazard Information | Back Directory | [Uses]
H-Ser-Pro-OH is a dipeptide containing serine and proline, which can serve as a substrate for prolinase I (PD I) and PD II. H-Ser-Pro-OH can also be used for the synthesis of polypeptide[1][2]. | [Definition]
ChEBI: Ser-Pro is a dipeptide formed from L-serine and L-proline residues. It has a role as a metabolite. | [References]
[1] Liu G, et al. Prolidase isoenzymes in the rat: their organ distribution, developmental change and specific inhibitors. Pediatr Res. 2007 Jul;62(1):54-9. DOI:10.1203/PDR.0b013e3180676d05
[2] Sheikh IA, et al. Mechanism of digestion of bradykinin and lysylbradykinin (kallidin) in human serum. Role of carboxypeptidase, angiotensin-converting enzyme and determination of final degradation products. Biochem Pharmacol. 1989 Mar 15;38(6):993-1000. DOI:10.1016/0006-2952(89)90290-6 |
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