72978-16-6
72978-16-6
Chemical Structure
Δ1-Pyrroline-2-carboxylic acid sodium
Synonym(s): Pyr2C sodium
- CAS No.: 72978-16-6
- Formula:C5H6NNaO2
- Molecular Weight:135.10
InChIKey: QKIMVEBDSSQQKE-UHFFFAOYSA-M
SMILES: O=C(C1=NCCC1)O[Na]
Biological Activity: Δ1-Pyrroline-2-carboxylic acid (Pyr2C) sodium is a cyclic imino acid involved in proline metabolism. Within cells, Δ1-Pyrroline-2-carboxylic acid sodium can be directly reduced to proline, supporting the growth of proline-auxotrophic strains of Escherichia coli. Δ1-Pyrroline-2-carboxylic acid sodium also serves as an intermediate in organic synthesis and can be used to synthesize L-pipecolic acid (HY-W012734)[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Δ1-Pyrroline-2-carboxylic acid sodium | 98.03% | Δ1-Pyrroline-2-carboxylic acid (Pyr2C) sodium is a cyclic imino acid involved in proline metabolism. Within cells, Δ1-Pyrroline-2-carboxylic acid sodium can be directly reduced to proline, supporting the growth of proline-auxotrophic strains of Escherichia coli. Δ1-Pyrroline-2-carboxylic acid sodium also serves as an intermediate in organic synthesis and can be used to synthesize L-pipecolic acid (HY-W012734). | ||||||||||||||||||||
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References
- [1]. Mark L. Lewis, et al. The effect of pH on the solution structure of Δ1-pyrroline-2-carboxylic acid as revealed by NMR and electrospray mass spectroscopy. Bioorganic & Medicinal Chemistry Letters, June 1993.
- [2]. Kaja Stalder, et al. Biocatalytic Synthesis of l-Pipecolic Acid by a Lysine Cyclodeaminase: Batch and Flow Reactors. ChemCatChem 2024, e202301671.
