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Catalog Number:
26442
CAS Number:
313232-63-2
Ácido S - N -Fmoc- N , N -bis-Boc-2-amino-3-guanidinopropiónico
Purity:
≥ 97 % (HPLC)
Synonym(s):
Fmoc-L-Agp(Boc) 2 -OH
Documents
$40.30 /100 mg
Tamaño
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Product Information

(S)-N-Fmoc-N,N'-bis-Boc-2-amino-3-guanidino propionic acid is a versatile compound widely utilized in peptide synthesis and drug development. This amino acid derivative features a unique structure that enhances its stability and solubility, making it an ideal choice for researchers in the fields of biochemistry and medicinal chemistry. Its Fmoc (9-fluorenylmethoxycarbonyl) and Boc (tert-butyloxycarbonyl) protecting groups facilitate the selective modification of amino acids, allowing for the efficient assembly of complex peptides.

This compound is particularly valuable in the design of peptide-based therapeutics and can be employed in the development of inhibitors, vaccines, and other bioactive molecules. Its ability to form stable interactions with biological targets enhances its potential in drug discovery. Researchers appreciate its compatibility with various coupling reagents and its effectiveness in solid-phase peptide synthesis, making it a preferred choice for both academic and industrial applications.

Synonyms
Fmoc-L-Agp(Boc) 2 -OH
CAS Number
313232-63-2
Purity
≥ 97 % (HPLC)
Molecular Formula
C29H36N4O8
Molecular Weight
568.62
MDL Number
MFCD01632272
PubChem ID
75627335
Appearance
Polvo cristalino de color blanco a blanquecino.
Optical Rotation
[a] D 20 = -7,5 a -11,5 º (C=1 en MeOH)
Conditions
Conservar a ≤ -15 °C
General Information
Synonyms
Fmoc-L-Agp(Boc) 2 -OH
CAS Number
313232-63-2
Purity
≥ 97 % (HPLC)
Molecular Formula
C29H36N4O8
Molecular Weight
568.62
MDL Number
MFCD01632272
PubChem ID
75627335
Appearance
Polvo cristalino de color blanco a blanquecino.
Optical Rotation
[a] D 20 = -7,5 a -11,5 º (C=1 en MeOH)
Conditions
Conservar a ≤ -15 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(S)-N-Fmoc-N,N'-bis-Boc-2-amino-3-guanidino propionic acid is widely utilized in research focused on

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in the development of therapeutic agents. Its protective groups facilitate selective reactions, enhancing yield and purity.
  • Drug Development: In pharmaceutical research, it is employed to create novel drug candidates that target specific biological pathways, making it valuable for developing treatments for various diseases.
  • Bioconjugation: The compound can be used in bioconjugation processes, allowing researchers to attach biomolecules to surfaces or other molecules, which is crucial in diagnostics and targeted drug delivery systems.
  • Research in Protein Engineering: It aids in the design of modified proteins, enabling scientists to explore protein functions and interactions, which is essential for understanding biological mechanisms.
  • Development of Antibody-Drug Conjugates: This chemical plays a role in creating antibody-drug conjugates, which combine antibodies with cytotoxic drugs to improve the specificity and efficacy of cancer treatments.

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