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

Catalog Number:
02268
CAS Number:
3556-56-7
Z-L-tyrosine 4-nitrophenyl ester
Purity:
≥ 97%
Synonym(s):
Z-L-Tyr-ONp
Documents
$36.65 /1G
Pack Size Availability Price
Request Bulk Quote
Product Information

Z-L-tyrosine 4-nitrophenyl ester is a versatile compound widely utilized in biochemical research and pharmaceutical applications. This ester derivative of tyrosine features a nitrophenyl group, enhancing its reactivity and making it an excellent substrate for various enzymatic reactions. Researchers often employ Z-L-tyrosine 4-nitrophenyl ester in the synthesis of peptide bonds and as a building block in the development of novel pharmaceuticals. Its unique structure allows for selective modifications, which can lead to the creation of compounds with tailored biological activities.

In addition to its applications in peptide synthesis, Z-L-tyrosine 4-nitrophenyl ester serves as a valuable tool in the study of enzyme kinetics and mechanisms. Its ability to release tyrosine upon hydrolysis makes it an effective probe for investigating the activity of proteolytic enzymes. This compound's stability and solubility in various solvents further enhance its usability in laboratory settings, making it a preferred choice for researchers seeking reliable and efficient reagents for their experiments.

Synonyms
Z-L-Tyr-ONp
CAS Number
3556-56-7
Purity
≥ 97%
Molecular Formula
C23H20N2O7
Molecular Weight
436.4
MDL Number
MFCD00024659
PubChem ID
98200
Conditions
Store at 0-8°C
General Information
Synonyms
Z-L-Tyr-ONp
CAS Number
3556-56-7
Purity
≥ 97%
Molecular Formula
C23H20N2O7
Molecular Weight
436.4
MDL Number
MFCD00024659
PubChem ID
98200
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Z-L-tyrosine 4-nitrophenyl ester is widely utilized in research focused on:

  • Biochemical Research: This compound serves as a substrate in enzyme assays, helping researchers study the activity of various enzymes involved in metabolic pathways.
  • Drug Development: Its properties make it a valuable intermediate in synthesizing pharmaceuticals, particularly those targeting neurological disorders due to its structural similarity to neurotransmitters.
  • Protein Engineering: Used in the modification of proteins, this ester can enhance the solubility and stability of therapeutic proteins, improving their efficacy in medical applications.
  • Analytical Chemistry: It acts as a standard in chromatographic techniques, allowing for the accurate quantification of tyrosine derivatives in complex biological samples.
  • Cosmetic Formulations: The compound is incorporated into skincare products for its antioxidant properties, contributing to formulations aimed at reducing oxidative stress on the skin.

Citations