Results 1 to 10 of about 1,076,842 (263)

Combinatorial chemistry in drug discovery. [PDF]

open access: yesCurr Opin Chem Biol, 2017
Several combinatorial methods have been developed to create focused or diverse chemical libraries with a wide range of linear or macrocyclic chemical molecules: peptides, non-peptide oligomers, peptidomimetics, small-molecules, and natural product-like organic molecules.
Liu R, Li X, Lam KS.
europepmc   +7 more sources

Protein-Directed Dynamic Combinatorial Chemistry: A Guide to Protein Ligand and Inhibitor Discovery [PDF]

open access: yesMolecules, 2016
Protein-directed dynamic combinatorial chemistry is an emerging technique for efficient discovery of novel chemical structures for binding to a target protein.
Renjie Huang, Ivanhoe K. H. Leung
doaj   +3 more sources

Virtual Combinatorial Chemistry and Pharmacological Screening: A Short Guide to Drug Design. [PDF]

open access: yesInt J Mol Sci, 2022
Traditionally, drug development involved the individual synthesis and biological evaluation of hundreds to thousands of compounds with the intention of highlighting their biological activity, selectivity, and bioavailability, as well as their low ...
Suay-García B   +4 more
europepmc   +2 more sources

Protein-Templated Dynamic Combinatorial Chemistry: Brief Overview and Experimental Protocol. [PDF]

open access: yesEuropean J Org Chem, 2019
Dynamic combinatorial chemistry (DCC) is a powerful tool to identify bioactive compounds. This efficient technique allows the target to select its own binders and circumvents the need for synthesis and biochemical evaluation of all individual derivatives.
Hartman AM, Gierse RM, Hirsch AKH.
europepmc   +2 more sources

Fragment Linking and Optimization of Inhibitors of the Aspartic Protease Endothiapepsin: Fragment-Based Drug Design Facilitated by Dynamic Combinatorial Chemistry. [PDF]

open access: yesAngew Chem Int Ed Engl, 2016
Fragment‐based drug design (FBDD) affords active compounds for biological targets. While there are numerous reports on FBDD by fragment growing/optimization, fragment linking has rarely been reported.
Mondal M   +5 more
europepmc   +2 more sources

Combinatorial Chemistry

open access: yesCHIMIA, 2000
In many areas of chemical synthesis, drug discovery, and materials research, combinatorial approaches are becoming more and more important. One of the most serious bottlenecks in this area is the chemical analysis and screening of the products ...
Renato Zenobi
doaj   +4 more sources

Structurally divergent dynamic combinatorial chemistry on racemic mixtures [PDF]

open access: yesNature Communications, 2020
Structurally divergent reactions on racemic mixtures, which produce distinct chemical species from an enantiomeric mixture, are extremely rare in the literature.
Tiberiu-M. Gianga, G. Dan Pantoș
doaj   +2 more sources

The Effects of Combinatorial Chemistry and Technologies on Drug Discovery and Biotechnology – a Mini Review

open access: yesNova Biotechnologica et Chimica, 2014
The review will focus on the aspects of combinatorial chemistry and technologies that are more relevant in the modern pharmaceutical process. An historical, critical introduction is followed by three chapters, dealing with the use of combinatorial ...
Seneci Pierfausto   +3 more
doaj   +2 more sources

Mesofluidic devices for DNA-programmed combinatorial chemistry. [PDF]

open access: yesPLoS ONE, 2012
Hybrid combinatorial chemistry strategies that use DNA as an information-carrying medium are proving to be powerful tools for molecular discovery. In order to extend these efforts, we present a highly parallel format for DNA-programmed chemical library ...
Rebecca M Weisinger   +3 more
doaj   +2 more sources

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