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| | H-Ser-Pro-OH Basic information |
| Product Name: | H-Ser-Pro-OH | | Synonyms: | L-SERYL-L-PROLINE;1-(L-Seryl)-L-proline;1-Serylproline;L-Ser-L-Pro-OH;(S)-1-((S)-2-Amino-3-hydroxypropanoyl)pyrrolidine-2-carboxylic acid;L-Proline, L-seryl-;H2N-Ser-Pro-COOH;Ser-Pro-OH | | CAS: | 23827-93-2 | | MF: | C8H14N2O4 | | MW: | 202.21 | | EINECS: | | | Product Categories: | | | Mol File: | 23827-93-2.mol |  |
| | H-Ser-Pro-OH Chemical Properties |
| 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 |
| | H-Ser-Pro-OH Usage And Synthesis |
| 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 |
| | H-Ser-Pro-OH Preparation Products And Raw materials |
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