DL-Proline

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].

Product Specifications

CAS Number

[609-36-9]

UNSPSC

12352209

Hazard Statement

H302, H315, H319, H335

Target

Biochemical Assay Reagents

Type

Peptides

Related Pathways

Others

Field of Research

Cancer; Infection

Assay Protocol

https://www.medchemexpress.com/h-dl-pro-oh.html

Purity

98.0

Solubility

H2O : 100 mg/mL (ultrasonic)

Smiles

OC(=O)C1CCCN1

Molecular Formula

C5H9NO2

Molecular Weight

115.13

Precautions

H302, H315, H319, H335

References & Citations

[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.