52899-09-9
52899-09-9
Chemical Structure
H-Pro-Val-OH
Synonym(s): Pro-Val
- CAS No.: 52899-09-9
- Formula:C10H18N2O3
- Molecular Weight:214.26
InChIKey: AWJGUZSYVIVZGP-YUMQZZPRSA-N
SMILES: CC(C)[C@@H](C(O)=O)NC([C@H]1NCCC1)=O
Biological Activity: 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].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
H-Pro-Val-OH | 99.34% | 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. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
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. [Content Brief]
- [2]. Davie EA, et al. Asymmetric catalysis mediated by synthetic peptides. Chem Rev. 2007 Dec;107(12):5759-812. [Content Brief]
- [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. [Content Brief]
- [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. [Content Brief]
Keywords
