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Catalog Number:
07061
CAS Number:
252029-00-8
(2 S ,4 S )-Fmoc-(4-FmocNH)homoprolina
Purity:
≥ 99 % (HPLC)
Synonym(s):
Fmoc-HoPro(Fmoc)-OH
Documents
$79.22 /100 mg
Tamaño
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Product Information

The compound (2S,4S)-Fmoc-(4-FmocNH)homoproline is a valuable building block in peptide synthesis, particularly in the development of peptide-based therapeutics and research applications. This compound features a unique structure that enhances its utility in solid-phase peptide synthesis, allowing for the efficient incorporation of homoproline residues into peptides. Its Fmoc (9-fluorenylmethoxycarbonyl) protecting groups facilitate easy deprotection under mild conditions, making it an ideal choice for researchers looking to streamline their synthesis processes.

In addition to its role in peptide synthesis, (2S,4S)-Fmoc-(4-FmocNH)homoproline has shown promise in the design of bioactive peptides, which can be utilized in drug discovery and development. The compound's ability to introduce conformational rigidity into peptide chains can lead to improved binding affinities and specificity for biological targets. Researchers in medicinal chemistry and biochemistry will find this compound particularly beneficial for creating novel peptide sequences with enhanced therapeutic potential.

Synonyms
Fmoc-HoPro(Fmoc)-OH
CAS Number
252029-00-8
Purity
≥ 99 % (HPLC)
Molecular Formula
C36H32N2O6
Molecular Weight
588.66
MDL Number
MFCD02259485
Appearance
Polvo blanquecino
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Fmoc-HoPro(Fmoc)-OH
CAS Number
252029-00-8
Purity
≥ 99 % (HPLC)
Molecular Formula
C36H32N2O6
Molecular Weight
588.66
MDL Number
MFCD02259485
Appearance
Polvo blanquecino
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(2S,4S)-Fmoc-(4-FmocNH)homoproline 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 cyclic peptides, which are important for drug discovery and development.
  • Drug Development: Its unique structure allows researchers to modify peptides for better binding affinity and specificity, making it valuable in the pharmaceutical industry for creating targeted therapies.
  • Bioconjugation: The compound is used in bioconjugation techniques, enabling the attachment of drugs or imaging agents to biomolecules, enhancing the effectiveness of treatments.
  • Research in Protein Engineering: It is instrumental in studies aimed at modifying protein structures, which can lead to advancements in enzyme design and therapeutic proteins.
  • Academic Research: This chemical is frequently employed in academic laboratories for studies related to amino acid properties and their influence on protein folding and stability.

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