| Identification | Back Directory | [Name]
H-PRO-VAL-OH | [CAS]
52899-09-9 | [Synonyms]
PRO-VAL
H-PRO-VAL-OH
PROLINE-VALINE
L-Propyl-L-valine
L-PROLYL-L-VALINE
L-Valine, L-prolyl- | [Molecular Formula]
C10H18N2O3 | [MDL Number]
MFCD00037867 | [MOL File]
52899-09-9.mol | [Molecular Weight]
214.26 |
| Chemical Properties | Back Directory | [Melting point ]
221 °C | [Boiling point ]
451.1±45.0 °C(Predicted) | [density ]
1.150±0.06 g/cm3(Predicted) | [storage temp. ]
-15°C
| [pka]
3.54±0.10(Predicted) | [Sequence]
Pro-Val |
| Hazard Information | Back Directory | [Uses]
H-Pro-Val-OH is a deprotonation dipeptide containing proline, which can catalyze the Michael addition reaction of acetone to trans-β-nitrostyrene. H-Pro Val OH can also serve as a substrate for fibroblast enzymes and prolinase, and has potential applications in biochemical analysis[1][2][3][4]. | [References]
[1] Harrison AG, et al. Fragmentation reactions of deprotonated peptides containing proline. The proline effect. J Mass Spectrom. 2005 Sep;40(9):1173-86. DOI:10.1002/jms.891
[2] Davie EA, et al. Asymmetric catalysis mediated by synthetic peptides. Chem Rev. 2007 Dec;107(12):5759-812. DOI:10.1021/cr068377w
[3] Uramatsu M, et al. Different effects of sulfur amino acids on prolidase and prolinase activity in normal and prolidase-deficient human erythrocytes. Clin Chim Acta. 2007 Jan;375(1-2):129-35. DOI:10.1016/j.cca.2006.06.027
[4] Myara I, et al. Determination of prolinase activity in plasma. Application to liver disease and its relation with prolidase activity. Clin Biochem. 1985 Aug;18(4):220-3. DOI:10.1016/s0009-9120(85)80043-6 |
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