structure of 203854-47-1

(3S)-7-[[(1,1-Dimethylethoxy)carbonyl]amino]-3-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]heptanoic acid

CAS No.: 203854-47-1 Brand: MolBest
M. Ft.: C27H34N2O6 Cat. No: G8671383
M. Wt.: 482.57 MDL: No record
Storage: 2-8°C
Purity Grade Package Stock Price Quantity
98% RG 100MG In Stock 10 USD
98% RG 250MG In Stock 17 USD
98% RG 1G In Stock 44 USD
98% RG 5G In Stock 195 USD
98% RG 25G In Stock 1713 USD
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Applications of 203854-47-1

(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-7-((tert-butoxycarbonyl)amino)heptanoic acid finds applications in:

  • Peptide Synthesis: It serves as a key intermediate in the synthesis of various peptides used in research and therapeutic applications.
  • Drug Development: Its derivatives are explored for potential pharmaceutical applications, particularly in oncology and infectious diseases.
  • Bioconjugation Techniques: This compound is utilized in bioconjugation strategies to attach biomolecules for targeted drug delivery systems.

Biological Activity of 203854-47-1

The biological activity of (S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-7-((tert-butoxycarbonyl)amino)heptanoic acid is primarily linked to its role as a building block in peptide synthesis. Compounds derived from this structure have been shown to exhibit various biological properties, including:

  • Antimicrobial Activity: Certain peptides synthesized from this compound have demonstrated effectiveness against bacterial strains.
  • Anticancer Properties: Peptides containing this amino acid derivative have been investigated for their potential to inhibit tumor growth and induce apoptosis in cancer cells.
  • Enzyme Inhibition: Some derivatives may act as inhibitors for specific enzymes, contributing to their therapeutic potential.

NMR spectrum of 203854-47-1

Physical sample testing spectrum (NMR) of 203854-47-1

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