It is a key building block that protects the proline residue during peptide assembly and can be used to selectively deprotect and add other amino acids. In research, it has been studied for its ability to inhibit the enzyme prolidase, which is involved in diseases like prolidase deficiency. N-Benzyloxycarbonyl-L-proline serves as a protected amino acid in custom peptide synthesis to build specific peptide chains, and as a prolidase inhibitor in biological and pharmaceutical research.
Benzyloxycarbonyl-l-proline
| API Name | Acalabrutinib |
|---|---|
| CAS No | 1148-11-4 |
| Molecular Formula | C13H15NO4 |
| Molecular Weight | 249.26 g/mol |
| Synonyms | (2S)-1-phenylmethoxycarbonylpyrrolidine-2-carboxylic acid |
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Frequently Asked Questions
It is a key building block that protects the proline residue during peptide assembly and can be used to selectively deprotect and add other amino acids. In research, it has been studied for its ability to inhibit the enzyme prolidase, which is involved in diseases like prolidase deficiency. N-Benzyloxycarbonyl-L-proline serves as a protected amino acid in custom peptide synthesis to build specific peptide chains, and as a prolidase inhibitor in biological and pharmaceutical research.
The CAS number of Benzyloxycarbonyl-l-proline is 1148-11-4.
The molecular formula of Benzyloxycarbonyl-l-proline is C13H15NO4.
The listed molecular weight of Benzyloxycarbonyl-l-proline is 249.26 g/mol.
Benzyloxycarbonyl-l-proline is listed as being used in connection with the following API: Acalabrutinib.
The listed synonym or IUPAC name for Benzyloxycarbonyl-l-proline is (2S)-1-phenylmethoxycarbonylpyrrolidine-2-carboxylic acid.