Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
05787
CAS Number:
2643-70-1
γ-Glu-4-Abz-OH
Purity:
≥ 98% (NMR)
Synonym(s):
H-Glu(4-Abz-OH)-OH, H-L-Glu(4-Abz-OH)-OH
Documents
$101.75 /100MG
Pack Size Availability Price
Request Bulk Quote
Product Information

g-Glu-4-Abz-OH, also known as 4-[(4S)-4-amino-4-carboxybutanoyl]amino]benzoic acid, is a specialized compound that plays a significant role in biochemical research and applications. This amino acid derivative is particularly valuable in the synthesis of peptide-based drugs and in the development of targeted therapies. Its unique structure allows for enhanced interactions with biological systems, making it an ideal candidate for studies in drug design and delivery. Researchers utilize g-Glu-4-Abz-OH for its ability to serve as a building block in the formation of bioactive peptides, which can be tailored for specific therapeutic functions, including anti-cancer and anti-inflammatory properties.

The compound's versatility extends to its use in various analytical techniques, such as chromatography and mass spectrometry, where it can aid in the identification and quantification of complex biomolecules. Additionally, g-Glu-4-Abz-OH's stability and solubility in aqueous solutions make it suitable for in vitro studies, allowing scientists to explore its potential in drug formulation and development. By incorporating this compound into their research, professionals can leverage its unique properties to advance their work in medicinal chemistry and biochemistry.

Synonyms
H-Glu(4-Abz-OH)-OH, H-L-Glu(4-Abz-OH)-OH
CAS Number
2643-70-1
Purity
≥ 98% (NMR)
Molecular Formula
C12H14N2O5
Molecular Weight
266.25
MDL Number
MFCD00038802
PubChem ID
12833031
Melting Point
230 - 232 °C
Appearance
White to off-white solid
Optical Rotation
[a]D20 = 13 ± 1 º (C = 4 in 5% Sodium Carbonate)
Conditions
Store at 0 - 8 °C
General Information
Synonyms
H-Glu(4-Abz-OH)-OH, H-L-Glu(4-Abz-OH)-OH
CAS Number
2643-70-1
Purity
≥ 98% (NMR)
Molecular Formula
C12H14N2O5
Molecular Weight
266.25
MDL Number
MFCD00038802
PubChem ID
12833031
Melting Point
230 - 232 °C
Appearance
White to off-white solid
Optical Rotation
[a]D20 = 13 ± 1 º (C = 4 in 5% Sodium Carbonate)
Conditions
Store at 0 - 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

g-Glu-4-Abz-OH is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, allowing researchers to create custom peptides for various applications in drug development and biotechnology.
  • Fluorescent Probes: It is used in the development of fluorescent probes for biological imaging, enabling scientists to visualize cellular processes in real-time with high specificity.
  • Drug Delivery Systems: g-Glu-4-Abz-OH can be incorporated into drug delivery systems, enhancing the targeting and release profiles of therapeutic agents, which is crucial in cancer treatment.
  • Bioconjugation: This compound is valuable for bioconjugation techniques, allowing for the attachment of biomolecules to surfaces or other molecules, facilitating the study of protein interactions.
  • Research in Neurobiology: It plays a role in neurobiological studies, particularly in the development of compounds that can modulate neurotransmitter activity, contributing to advancements in understanding neurological disorders.

Citations