Fmoc-Asp(EDANS)-OH
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Fmoc-Asp(EDANS)-OH

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Category
Fmoc-Amino Acids
Catalog number
BAT-005297
CAS number
182253-73-2
Molecular Formula
C31H29N3O8S
Molecular Weight
603.64
Fmoc-Asp(EDANS)-OH
IUPAC Name
(2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-4-oxo-4-[2-[(5-sulfonaphthalen-1-yl)amino]ethylamino]butanoic acid
Synonyms
N2-(((9H-fluoren-9-yl)methoxy)carbonyl)-N4-(2-((5-sulfonaphthalen-1-yl)amino)ethyl)-L-asparagine; (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-4-oxo-4-[2-[(5-sulfonaphthalen-1-yl)amino]ethylamino]butanoic acid
Purity
≧ 95%
InChI
InChI=1S/C31H29N3O8S/c35-29(33-16-15-32-26-13-5-12-24-23(26)11-6-14-28(24)43(39,40)41)17-27(30(36)37)34-31(38)42-18-25-21-9-3-1-7-19(21)20-8-2-4-10-22(20)25/h1-14,25,27,32H,15-18H2,(H,33,35)(H,34,38)(H,36,37)(H,39,40,41)/t27-/m0/s1
InChI Key
ZHXKVZRMHMFRBQ-MHZLTWQESA-N
Canonical SMILES
C1=CC=C2C(=C1)C(C3=CC=CC=C32)COC(=O)NC(CC(=O)NCCNC4=CC=CC5=C4C=CC=C5S(=O)(=O)O)C(=O)O

Fmoc-Asp(EDANS)-OH, a fluorophore-labeled amino acid derivative, plays a pivotal role in biochemical and biophysical research. Here are four key applications of Fmoc-Asp(EDANS)-OH, presented with high perplexity and burstiness:

Peptide Synthesis: Employing Fmoc-Asp(EDANS)-OH in solid-phase peptide synthesis facilitates the integration of fluorescence labels into peptides. This method enables researchers to meticulously monitor and measure peptide interactions and localization within intricate biological systems. By lending a fluorescence signal, these labeled peptides become indispensable tools in a multitude of binding assays and imaging studies, shedding light on complex biological processes.

FRET Studies: In the realm of Förster Resonance Energy Transfer (FRET) experiments, Fmoc-Asp(EDANS)-OH takes on the role of a donor fluorophore. When coupled with a suitable acceptor fluorophore, it enables the precise measurement of distances and conformational alterations within biomolecules. This application is pivotal in investigating protein-protein interactions, enzyme mechanisms, and the dynamics of nucleic acids.

Protein Structure and Dynamics: By incorporating Fmoc-Asp(EDANS)-OH into proteins, researchers can delve into the structural and dynamic aspects of proteins using fluorescence techniques. By closely monitoring changes in fluorescence signals, scientists are able to explore processes such as folding/unfolding, conformational shifts, and protein-ligand interactions. This deep dive provides valuable insights into the functionality and stability of proteins.

Bioassays: The usage of Fmoc-Asp(EDANS)-OH in the development of fluorescence-based bioassays for detecting various analytes stands as a hallmark application. In these innovative assays, the alteration in fluorescence upon analyte binding can be meticulously tracked, offering a sensitive and quantitative mode of detection. Widely embraced in diagnostics, drug discovery, and environmental monitoring, this application showcases the versatility and impact of Fmoc-Asp(EDANS)-OH in advancing various fields of research and analysis.

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