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Catalog Number:
32796
CAS Number:
152390-46-0
4-Nitro-Z-Gly-Cys(7-nitro-benzo[2,1,3]oxadiazol-4-yl)-Gly-OH
Synonym(s):
4-Nitro-Z-Gly-Cys(NBD)-Gly-OH, 4-Nitro-Z-Gly-Cys(7-nitrobenzofurazan-4-yl)-Gly-OH
Documents
$874.91 /25MG
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Product Information

4-Nitro-Z-Gly-Cys(7-nitro-benzo[2,1,3]oxadiazol-4-yl)-Gly-OH is a specialized compound known for its unique properties that make it valuable in various research and industrial applications. This compound features a nitro group and a benzo[2,1,3]oxadiazol moiety, which contribute to its fluorescence and reactivity, making it an excellent candidate for use in bioimaging and as a fluorescent probe in biochemical assays. Researchers can leverage its properties for studying protein interactions, cellular processes, and other biochemical phenomena, enhancing the understanding of complex biological systems.

In addition to its applications in research, 4-Nitro-Z-Gly-Cys(7-nitro-benzo[2,1,3]oxadiazol-4-yl)-Gly-OH can be utilized in the development of novel therapeutic agents and diagnostic tools. Its ability to selectively bind to specific biomolecules opens avenues for targeted drug delivery and the design of innovative diagnostic assays. With its unique structure and functional capabilities, this compound stands out in the field of chemical research, offering significant advantages over similar compounds in terms of specificity and sensitivity.

Synonyms
4-Nitro-Z-Gly-Cys(NBD)-Gly-OH, 4-Nitro-Z-Gly-Cys(7-nitrobenzofurazan-4-yl)-Gly-OH
CAS Number
152390-46-0
Molecular Formula
C21H19N7O11S
Molecular Weight
577.49
MDL Number
MFCD00237196
Conditions
Store at ≤ -10 °C
General Information
Synonyms
4-Nitro-Z-Gly-Cys(NBD)-Gly-OH, 4-Nitro-Z-Gly-Cys(7-nitrobenzofurazan-4-yl)-Gly-OH
CAS Number
152390-46-0
Molecular Formula
C21H19N7O11S
Molecular Weight
577.49
MDL Number
MFCD00237196
Conditions
Store at ≤ -10 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

4-Nitro-Z-Gly-Cys(7-nitro-benzo[2,1,3]oxadiazol-4-yl)-Gly-OH is widely utilized in research focused on:

  • Fluorescent Labeling: This compound is effective for labeling biomolecules in live-cell imaging, allowing researchers to track cellular processes in real-time.
  • Bioconjugation: It serves as a versatile linker in bioconjugation techniques, facilitating the attachment of drugs or probes to proteins for targeted delivery in therapeutic applications.
  • Protein Interaction Studies: The compound is used in assays to study protein-protein interactions, providing insights into cellular mechanisms that can lead to drug discovery.
  • Diagnostics Development: It plays a role in developing diagnostic tools by enhancing the sensitivity of detection methods, which is crucial for early disease diagnosis.
  • Research in Neuroscience: This chemical is valuable in neuroscience research for studying neurotransmitter release and neuronal signaling, contributing to the understanding of brain functions.

Citations