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Catalog Number:
02129
CAS Number:
127862-89-9
ZL-homophénylalanine
Purity:
≥ 99 % (HPLC)
Synonym(s):
ZL-HomoPhe-OH, ( Acide S -2-(Z-amino)-4-phénylbutyrique
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Product Information

Z-L-homophenylalanine is a valuable amino acid derivative widely recognized for its applications in peptide synthesis and pharmaceutical research. This compound, also known as Z-Homophenylalanine, serves as a crucial building block in the development of peptide-based therapeutics, particularly in the design of inhibitors and biologically active molecules. Its unique structure, featuring a phenyl group, enhances its ability to mimic natural amino acids, making it an essential component in the synthesis of peptides that require specific structural characteristics for biological activity.

Researchers and industry professionals utilize Z-L-homophenylalanine for its ability to improve the stability and efficacy of peptide drugs. Its incorporation into peptide sequences can lead to enhanced binding affinities and improved pharmacokinetic profiles. Additionally, this compound is instrumental in the study of protein folding and interactions, providing insights that are critical for drug development and biochemistry. With its versatile applications and significant benefits in the pharmaceutical and research sectors, Z-L-homophenylalanine stands out as a key player in advancing peptide chemistry.

Synonyms
ZL-HomoPhe-OH, ( Acide S -2-(Z-amino)-4-phénylbutyrique
CAS Number
127862-89-9
Purity
≥ 99 % (HPLC)
Molecular Formula
C 18 H 194
Molecular Weight
313.35
MDL Number
MFCD00038796
PubChem ID
5004209
Melting Point
101-107 °C
Optical Rotation
[α] D 20 = -15 ± 2º (C=1% dans MeOH)
Conditions
Conserver à 0-8°C
General Information
Synonyms
ZL-HomoPhe-OH, ( Acide S -2-(Z-amino)-4-phénylbutyrique
CAS Number
127862-89-9
Purity
≥ 99 % (HPLC)
Molecular Formula
C 18 H 194
Molecular Weight
313.35
MDL Number
MFCD00038796
PubChem ID
5004209
Melting Point
101-107 °C
Optical Rotation
[α] D 20 = -15 ± 2º (C=1% dans MeOH)
Conditions
Conserver à 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Z-L-homophenylalanine is widely utilized in research focused on

  • Peptide Synthesis: This compound serves as a valuable building block in the synthesis of peptides, particularly in the development of therapeutic proteins and biologics.
  • Drug Development: It is used in the design of novel pharmaceuticals, especially those targeting specific receptors, due to its ability to mimic natural amino acids.
  • Biotechnology: Researchers employ Z-L-homophenylalanine in various biotechnological applications, including enzyme engineering and the production of bioactive compounds.
  • Protein Engineering: This chemical aids in modifying protein structures to enhance stability and activity, making it essential in the field of protein design.
  • Research in Neuroscience: Its unique properties allow for exploration in neurobiology, particularly in studying neurotransmitter functions and interactions.

Citations