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L-Proline

Catalog No.
C6101
An amino acid used for collagen synthesis and maintaining the function of joints and tendons.
Grouped product items
SizePriceStock Qty
50g
$50.00
In stock
100g
$75.00
In stock
For scientific research use only and should not be used for diagnostic or medical purposes.

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Background

L-Proline (CAS No.: 147-85-3) is a nonessential amino acid that serves as a fundamental building block of proteins and is biosynthesized from glutamic acid in living systems. Distinguished by its unique cyclic structure that constrains backbone flexibility, L-proline plays a critical role in modulating protein conformation, frequently inducing bends and turns in secondary structures and thereby influencing protein folding and stability. It is a major component of collagen, contributing to the structural integrity of connective tissues such as joints and tendons, and is widely studied in the context of extracellular matrix biology and tissue remodeling. In cellular systems, L-proline functions as a substrate for the proton-coupled amino acid transporter 1 (PAT1) and has been identified as a low micromolar inhibitor of acetylcholinesterase, suggesting potential relevance in neuromodulatory research. Additionally, it is implicated in redox homeostasis, osmoprotection, and metabolic adaptation, with well-documented roles in stress response pathways, particularly in plant and cellular stress models. In biomedical research and drug discovery, L-proline is commonly utilized in studies of protein engineering, folding dynamics, and metabolic regulation, as well as in screening platforms investigating transporter activity and enzyme inhibition, where experimental concentrations are selected according to specific assay conditions and study objectives.

Chemical Properties

Physical AppearanceA solid
Storage-20°C
M.Wt115.13
Cas No.147-85-3
FormulaC5H9NO2
Synonyms(S)-(–)-Proline; L-(–)-Proline; NSC 46703
Solubilityinsoluble in DMSO; ≥11.27 mg/mL in EtOH with ultrasonic; ≥35.5 mg/mL in H2O
Chemical Name(S)-pyrrolidine-2-carboxylic acid
Canonical SMILESO=C1C=C[C@]2(C([C@H](C[C@@]3([C@@]2([C@H](C[C@]4([C@]3(CC[C@@]4(C(COC(CCC(O)=O)=O)=O)O)[H])C)O)[H])[H])C)=C1)C
Shipping ConditionSmall Molecules with Blue Ice, Modified Nucleotides with Dry Ice.
General tips We do not recommend long-term storage for the solution, please use it up soon.

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