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Catalog Number:
32809
CAS Number:
945414-97-1
Sel de trifluoroacétate de 6-(7-nitro-benzo[2,1,3]oxadiazol-4-ylamino)-hexanoyl-Arg-Pro-Lys-Pro-Leu-Ala-Nva-Trp-Lys((7-diméthylaminocoumarine-4-yl)-acétyl)-NH 2
Synonym(s):
NBD-ε-aminocaproyl-Arg-Pro-Lys-Pro-Leu-Ala-Nva-Trp-Lys(DMACA)-NH2
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Product Information

6-(7-Nitro-benzo[2,1,3]oxadiazol-4-ylamino)-hexanoyl-Arg-Pro-Lys-Pro-Leu-Ala-Nva-Trp-Lys((7-dimethyl is a specialized peptide compound that has garnered attention in the fields of biochemistry and molecular biology. This compound is particularly notable for its potential applications in drug development and targeted therapies, especially in cancer research. The incorporation of the 7-nitro-benzoxadiazol moiety enhances its fluorescent properties, making it an excellent candidate for use in bioimaging and as a tracer in various biological assays. Researchers can leverage its unique structure to study protein interactions, cellular processes, and the dynamics of signaling pathways.

Furthermore, the compound's peptide sequence is designed to facilitate specific interactions with biological targets, which can lead to improved efficacy in therapeutic applications. Its versatility allows for modifications that can tailor its properties for various experimental needs, making it a valuable tool for researchers aiming to explore complex biological systems. With its combination of fluorescence and bioactivity, this compound stands out as a promising candidate for advancing research in drug discovery and molecular diagnostics.

Synonyms
NBD-ε-aminocaproyl-Arg-Pro-Lys-Pro-Leu-Ala-Nva-Trp-Lys(DMACA)-NH2
CAS Number
945414-97-1
Molecular Formula
C 78 H 111 N 21 O 16
Molecular Weight
1598.87
MDL Number
MFCD18782547
Conditions
Conserver à ≤ -10 °C
General Information
Synonyms
NBD-ε-aminocaproyl-Arg-Pro-Lys-Pro-Leu-Ala-Nva-Trp-Lys(DMACA)-NH2
CAS Number
945414-97-1
Molecular Formula
C 78 H 111 N 21 O 16
Molecular Weight
1598.87
MDL Number
MFCD18782547
Conditions
Conserver à ≤ -10 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

6-(7-Nitro-benzo[2,1,3]oxadiazol-4-ylamino)-hexanoyl-Arg-Pro-Lys-Pro-Leu-Ala-Nva-Trp-Lys((7-dimethyl is widely utilized in research focused on:

  • Fluorescent Probes: This compound serves as a fluorescent probe in biological research, allowing scientists to visualize cellular processes and interactions in real-time. Its unique structure enhances fluorescence, making it ideal for imaging applications.
  • Drug Development: In pharmaceutical research, it is used to design peptide-based drugs. Its ability to mimic natural biological processes helps in creating more effective therapeutic agents, particularly in targeting specific diseases.
  • Bioconjugation: The compound is effective in bioconjugation techniques, where it can be attached to biomolecules for targeted delivery. This application is crucial in developing targeted therapies, especially in cancer treatment.
  • Diagnostic Tools: It finds application in the development of diagnostic tools, such as assays and biosensors. Its properties allow for the detection of specific biomolecules, aiding in early disease diagnosis.
  • Research in Neuroscience: The compound is utilized in neuroscience to study protein interactions and signaling pathways. Its ability to penetrate cell membranes makes it a valuable tool for exploring neuronal functions and disorders.

Citations