Results 31 to 40 of about 1,161,651 (341)

Stereochemical assignment of the protein-protein interaction inhibitor JBIR-22 by total synthesis [PDF]

open access: yes, 2015
The authors acknowledge the EPSRC and Cancer Research UK (CRUK Grant No. C21383/A6950) for funding this research.Recent reports have highlighted the biological activity associated with a sub-family of the tetramic acid class of natural products.
Healy, Alan   +4 more
core   +1 more source

Antimicrobial Activity of Amino Acid Analogues and Their Derivatives

open access: yesProceedings, 2017
Libraries of compounds containing unnatural amino acids or amino acid analogues were prepared from inexpensive substrates using sustainable processes [1–3]. [...]
Dácil Hernández   +4 more
doaj   +1 more source

Synthesis of Both Enantiomers of Chiral Phenylalanine Derivatives Catalyzed by Cinchona Alkaloid Quaternary Ammonium Salts as Asymmetric Phase Transfer Catalysts

open access: yesMolecules, 2018
A practical synthesis of both enantiomers of unnatural phenylalanine derivatives by using two pseudoenantiomeric phase transfer catalysts is described.
Lei Jin, Shuai Zhao, Xin Chen
doaj   +1 more source

Cell Surface Labeling of Escherichia coli via Copper(I)-Catalyzed [3+2] Cycloaddition [PDF]

open access: yes, 2003
Labeling of the cell surface of Escherichia coli was accomplished by expression of a recombinant outer membrane protein, OmpC, in the presence of the unnatural amino acid azidohomoalanine, which acts as a methionine surrogate.
Link, A. James, Tirrell, David A.
core   +1 more source

Protein engineering with unnatural amino acids

open access: yesCurrent Opinion in Structural Biology, 2013
Protein engineering has become an extensively used tool in many fields, allowing us to probe protein function, characterize proteins using a range of biophysical techniques, chemically modify proteins and improve protein function for medical and industrial applications.
Zhang, William   +2 more
openaire   +3 more sources

Synthesis of complex unnatural fluorine-containing amino acids [PDF]

open access: yesJournal of Fluorine Chemistry, 2020
The area of fluorinated amino acid synthesis has seen rapid growth over the past decade. As reports of singly fluorinated natural amino acid derivatives have grown, researchers have turned their attention to develop methodology to access complex proteinogenic examples.
William D.G. Brittain   +2 more
openaire   +3 more sources

Small Unnatural Amino Acid Carried Raman Tag for Molecular Imaging of Genetically Targeted Proteins.

open access: yesJournal of Physical Chemistry Letters, 2018
Raman has been implemented to image biological systems for decades. However, Raman microscopy along with Raman probes is restricted to image metabolites or a few intracellular organelles so far and lacks genetic specificity for imaging proteins of ...
Jing Zhang   +9 more
semanticscholar   +1 more source

A New Unnatural Amino Acid Derived from the Modification of 4′-(p-tolyl)-2,2′:6′,2″-terpyridine and Its Mixed-Ligand Complexes with Ruthenium: Synthesis, Characterization, and Photophysical Properties

open access: yesChemistry, 2023
The modification of the methyl group of 4′-(p-tolyl)-2,2′:6′,2″-terpyridine produced the novel unnatural amino acid 3-(4-([2,2′:6′,2″-terpyridin]-4′-yl)phenyl)-2-aminopropanoic acid (phet).
Konstantinos Ypsilantis   +5 more
doaj   +1 more source

Genetic Code Expansion of Vibrio natriegens

open access: yesFrontiers in Bioengineering and Biotechnology, 2021
Escherichia coli has been considered as the most used model bacteria in the majority of studies for several decades. However, a new, faster chassis for synthetic biology is emerging in the form of the fast-growing gram-negative bacterium Vibrio ...
Eden Ozer, Lital Alfonta
doaj   +1 more source

Site-Specific Incorporation of Selenocysteine by Genetic Encoding as a Photocaged Unnatural Amino Acid.

open access: yesBioconjugate chemistry, 2018
Selenocysteine (Sec) is a naturally occurring amino acid that is also referred to as the 21st amino acid. Site-specific incorporation of Sec into proteins is attractive, because the reactivity of a selenol group exceeds that of a thiol group and thus ...
Adarshi P. Welegedara   +4 more
semanticscholar   +1 more source

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