609-36-9
Chemical Structure
DL-Proline
- CAS No.: 609-36-9
- Formula:C5H9NO2
- Molecular Weight:115.13
IUPAC Name: proline
InChIKey: ONIBWKKTOPOVIA-UHFFFAOYSA-N
SMILES: OC(=O)C1CCCN1
Biological Activity: DL-Proline is a racemic mixture of D-Proline and L-Prolin. DL-Proline is a cyclic imino acid with a five-membered ring structure. DL-Proline is a key structural unit in peptide synthesis. DL-Proline can stabilize the β-turn conformation and affect the secondary structure of the peptide. DL-Proline has biological activities such as regulating peptide conformation and enhancing the stability of cyclic peptides. DL-Proline can be used to study diseases related to peptide structure and function, such as cancer and bacterial infection[1][2].
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DL-Proline | 98.0% | DL-Proline is a racemic mixture of D-Proline and L-Prolin. DL-Proline is a cyclic imino acid with a five-membered ring structure. DL-Proline is a key structural unit in peptide synthesis. DL-Proline can stabilize the β-turn conformation and affect the secondary structure of the peptide. DL-Proline has biological activities such as regulating peptide conformation and enhancing the stability of cyclic peptides. DL-Proline can be used to study diseases related to peptide structure and function, such as cancer and bacterial infection. | ||||||||||||||||||||
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DL-Proline-d3 | 99.67% | DL-Proline-d3 is the deuterium labeled DL-Proline. | ||||||||||||||||||||
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DL-Proline-2-d1 | 98.0% | DL-Proline-2-d is the deuterium labeled DL-Proline-2. | ||||||||||||||||||||
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DL-Proline-d7 | 98.0% | DL-Proline-d7 is the deuterium labeled DL-Proline (HY-W012908). H-DL-Pro-OH is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||||||||||||||||||||
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- [1]. Yan H, et al. Recent Progress in Solid‐Phase Total Synthesis of Naturally Occurring Small Peptides. Advanced Synthesis & Catalysis, 2022, 364(12): 1934-1961.
- [2]. Baron A, et al. cis-Apa: a practical linker for the microwave-assisted preparation of cyclic pseudopeptides via RCM cyclative cleavage. J Org Chem. 2011 Feb 4;76(3):766-72. [Content Brief]
