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Catalog Number:
02126
CAS Number:
21027-01-0
Z-Ala-Pro-OH
Purity:
99%
Synonym(s):
Z-L-alanyl-L-proline
Documents
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Product Information

Z-Ala-Pro-OH, also known as Z-α-Alanine-Proline-OH, is a valuable compound in the field of peptide synthesis and pharmaceutical research. This dipeptide derivative exhibits unique properties that make it an essential building block for the development of bioactive peptides and pharmaceuticals. Its structure, characterized by a pyrrolidine ring and a carboxylic acid group, enhances its stability and bioavailability, making it particularly useful in drug formulation. Researchers often utilize Z-Ala-Pro-OH in the synthesis of peptide-based therapeutics, where it can contribute to improved efficacy and reduced side effects compared to traditional compounds.

In addition to its applications in drug development, Z-Ala-Pro-OH is also employed in the study of protein folding and enzyme activity, providing insights into biochemical pathways and interactions. Its ability to mimic natural amino acids allows for the design of novel peptides with tailored properties, making it a versatile tool for chemists and biochemists alike. With its wide-ranging applications and benefits, Z-Ala-Pro-OH stands out as a key compound for professionals in the pharmaceutical and research industries.

Synonyms
Z-L-alanyl-L-proline
CAS Number
21027-01-0
Purity
99%
Molecular Formula
C16H20N2O5
Molecular Weight
320.35
MDL Number
MFCD00037335
PubChem ID
333210
Conditions
Store at -0°C.
General Information
Synonyms
Z-L-alanyl-L-proline
CAS Number
21027-01-0
Purity
99%
Molecular Formula
C16H20N2O5
Molecular Weight
320.35
MDL Number
MFCD00037335
PubChem ID
333210
Conditions
Store at -0°C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Z-Ala-Pro-OH is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a building block in the synthesis of peptides, particularly in the development of therapeutic agents. Its unique structure helps in creating peptides with specific biological activities.
  • Drug Development: Researchers use Z-Ala-Pro-OH in the formulation of new drugs, especially in the field of oncology and immunology, where modified peptides can enhance efficacy and reduce side effects.
  • Biotechnology: In biotechnological applications, this compound is employed in the design of enzyme inhibitors, which can be crucial for developing treatments for various diseases.
  • Research in Protein Folding: Z-Ala-Pro-OH is valuable in studies related to protein folding and stability, helping scientists understand how proteins achieve their functional forms.
  • Cosmetic Formulations: The compound is also explored in cosmetic chemistry for its potential benefits in skin care products, particularly for formulations aimed at enhancing skin hydration and elasticity.

Citations