Name: Fmoc-Val-Ala-aminomethyl acetate
Brand: BOC Sciences
Rating: 5 (1 reviews)

Synonyms

(5S,8S)-1-(9H-Fluoren-9-yl)-5-isopropyl-8-methyl-3,6,9-trioxo-2-oxa-4,7,10-triazaundecan-11-yl acetate

IUPAC Name

[[(2S)-2-[[(2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-methylbutanoyl]amino]propanoyl]amino]methyl acetate

Canonical SMILES

CC(C)C(C(=O)NC(C)C(=O)NCOC(=O)C)NC(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13

InChI

InChI=1S/C26H31N3O6/c1-15(2)23(25(32)28-16(3)24(31)27-14-35-17(4)30)29-26(33)34-13-22-20-11-7-5-9-18(20)19-10-6-8-12-21(19)22/h5-12,15-16,22-23H,13-14H2,1-4H3,(H,27,31)(H,28,32)(H,29,33)/t16-,23-/m0/s1

InChIKey

MZBRJYLMNFPXHD-HJPURHCSSA-N

Appearance

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Fmoc-Val-Ala-aminomethyl acetate, a versatile reagent utilized in peptide synthesis, boasts unique functionalities for chemical and pharmaceutical research. Here are four key applications of Fmoc-Val-Ala-aminomethyl acetate:

Synthetic Peptide Development: Central to solid-phase peptide synthesis (SPPS), Fmoc-Val-Ala-aminomethyl acetate plays a pivotal role in enabling chemists to intricately craft peptides with precise sequences. The Fmoc (9-fluorenylmethyloxycarbonyl) group acts as a shield for the amino terminus throughout synthesis, guaranteeing the methodical and sequential addition of amino acids.

Protein Engineering: Delving into the realm of protein engineering, researchers harness the power of Fmoc-Val-Ala-aminomethyl acetate to fashion peptides that either replicate protein structures or function as potent enzyme inhibitors. By integrating this reagent into synthetic peptides, scientists embark on a journey to explore protein interactions, stability, and enzymatic activity.

Drug Discovery: Within the domain of pharmaceutical exploration, Fmoc-Val-Ala-aminomethyl acetate emerges as a critical tool for constructing peptide libraries tailored for high-throughput screening. These libraries undergo rigorous screening against diverse biological targets to unearth potential drug candidates. The meticulous control over peptide synthesis facilitated by this reagent bolsters the discovery of peptides characterized by high specificity and potency.

Bioconjugation: Employed in cutting-edge bioconjugation methodologies, Fmoc-Val-Ala-aminomethyl acetate facilitates the seamless linkage of peptides to other biomolecules, such as antibodies or nanoparticles. This fusion is indispensable in sculpting targeted drug delivery systems and diagnostic aids. By affixing therapeutic peptides to targeting entities, researchers elevate the efficiency and specificity of drug delivery.