9-fluorenylmethoxycarbonyl

Known as: 9-Fmoc cpd 
 
National Institutes of Health

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9-fluorenylmethyloxycarbonyl chloride

Broader (1)

Fluorenes

Papers overview

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2009
2009
9-Fluorenylmethoxycarbonyl-labeled peptides as substrates in a capillary electrophoresis-based assay for sirtuin enzymes.
Sirtuins are the class III histone deacetylases that catalyze the deacetylation of acetyl-lysine residues of histones and other… (More)
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Highly Cited
2000
Highly Cited
2000
Rapid and general profiling of protease specificity by using combinatorial fluorogenic substrate libraries.
A method is presented for the preparation and use of fluorogenic peptide substrates that allows for the configuration of general… (More)
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Highly Cited
2000
Highly Cited
2000
Angiotensin I-converting enzyme inhibitory properties of whey protein digests: concentration and characterization of active peptides.
The aim of this study was to identify whey-derived peptides with angiotensin I-converting enzyme (ACE) inhibitory activity. The… (More)
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1995
1995
Sequence dependence of aspartimide formation during 9-fluorenylmethoxycarbonyl solid-phase peptide synthesis
We have examined the sequence dependence of aspartimide formation during Fmoc-based solid-phase synthesis of the peptide Val-Lys… (More)
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1995
1995
Antibody to ras proteins in patients with colon cancer.
The current study examined sera from 160 colon cancer patients and 60 normal individuals to determine whether antibody to mutated… (More)
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1993
1993
Solid-phase synthesis of oligonucleotides containing site-specific N-(2'-deoxyguanosin-8-yl)-2-(acetylamino)fluorene adducts using 9-fluorenylmethoxycarbonyl as the base-protecting group.
Eight oligodeoxyribonucleotides containing a site-specific N-(2'-deoxyguanosin-8-yl)-2-(acetyl-amino)fluorene (dG-C8-AAF) adduct… (More)
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1993
1993
Enhancement of peptide antigen presentation by a second peptide.
The influence of nonstimulatory "competitor" peptides on the binding of an antigenic peptide to a major histocompatibility… (More)
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1991
1991
Rapid "tea-bag" peptide synthesis using 9-fluorenylmethoxycarbonyl (Fmoc) protected amino acids applied for antigenic mapping of viral proteins.
The role of individual amino acids in binding human and macaque antibodies were determined in the human immunodeficiency virus… (More)
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Highly Cited
1990
Highly Cited
1990
A cleavage method which minimizes side reactions following Fmoc solid phase peptide synthesis.
The success of solid phase peptide synthesis utilizing 9-fluorenylmethoxycarbonyl (Fmoc) amino acids is often limited by… (More)
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1989
1989
Solid-phase synthesis of oligoribonucleotides using 9-fluorenylmethoxycarbonyl (Fmoc) for 5'-hydroxyl protection.
Efficient solid-phase synthesis of a series of oligoribonucleotides of up to 20 residues is described that utilises the 9… (More)
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