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Catalog Number:
06311
CAS Number:
214750-73-9
Nα-Fmoc-Nγ-(1-{1'-adamantyl}-1-methyl-ethoxycarbonyl)-L-2,4-diaminobutyric acid
Purity:
≥ 99% (HPLC, TLC)
Synonym(s):
Fmoc-L-Dab(Adpoc)-OH
Documents
$89.13 /100MG
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Product Information

Na-Fmoc-Ng-(1-{1'-adamantyl}-1-methyl-ethoxycarbonyl)-L-2,4-diaminobutyric acid is a versatile compound widely utilized in peptide synthesis and drug development. This amino acid derivative features a unique adamantyl group, which enhances its lipophilicity and stability, making it an excellent candidate for the design of bioactive peptides. Its Fmoc (9-fluorenylmethoxycarbonyl) protecting group allows for easy incorporation into peptide chains, facilitating the synthesis of complex molecules with improved pharmacological properties.

Researchers in medicinal chemistry and biochemistry can leverage this compound for the development of targeted therapies, particularly in the fields of cancer and infectious diseases. Its ability to form stable conjugates with various biomolecules opens avenues for innovative drug delivery systems. Additionally, the compound's unique structure may provide advantages over similar compounds in terms of solubility and cellular uptake, making it a valuable tool for scientists aiming to enhance the efficacy of therapeutic agents.

Synonyms
Fmoc-L-Dab(Adpoc)-OH
CAS Number
214750-73-9
Purity
≥ 99% (HPLC, TLC)
Molecular Formula
C33H40N2O6
Molecular Weight
560.5
MDL Number
MFCD01632073
PubChem ID
133108985
Appearance
White powder
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Fmoc-L-Dab(Adpoc)-OH
CAS Number
214750-73-9
Purity
≥ 99% (HPLC, TLC)
Molecular Formula
C33H40N2O6
Molecular Weight
560.5
MDL Number
MFCD01632073
PubChem ID
133108985
Appearance
White powder
Conditions
Store at 0 - 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Na-Fmoc-Ng-(1-{1'-adamantyl}-1-methyl-ethoxycarbonyl)-L-2,4-diaminobutyric acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in the synthesis of peptides, allowing for selective reactions and enhancing the yield of desired products.
  • Drug Development: Its unique structure aids in the design of novel pharmaceuticals, particularly in targeting specific biological pathways, making it valuable in medicinal chemistry.
  • Bioconjugation: The compound can be used to attach biomolecules to surfaces or other molecules, facilitating the development of targeted drug delivery systems.
  • Research in Neuroscience: It has potential applications in studying neuroprotective effects, as its derivatives may interact with neurological pathways, offering insights into treatments for neurodegenerative diseases.
  • Material Science: The compound can be incorporated into polymers for creating advanced materials with specific properties, such as improved thermal stability or enhanced mechanical strength.

Citations