The invention provides for in silico analysis of a virtual combinatorial library.
The present invention relates to a method of producing a dynamic combinatorial library of chemical compounds.
Nucleoside analog libraries are prepared in a combinatorial library approach.
Nucleoside analog libraries are prepared in a combinatorial library approach.
Deazapurine nucleoside analog libraries are prepared in a combinatorial library approach.
The invention provides for inexpensive and simple synthesis of a combinatorial chemical or biochemical library.
The present invention provides a variety of methods for synthesizing, encoding and decoding compounds in a combinatorial library.
The invention relates to a combinatorial library of compounds, characterized in that it comprises substituted derivatives of oxadiazolinone and/or oxadiazolinthione.
The invention also concerns a method for producing functional mosaic proteins, and for analysing a functional expression combinatorial library, by determining a sequential imprint for each of the mosaic proteins of the library.
Also disclosed is a combinatorial library of oligomers useful in the method and novel morpholino-subunit polymer compositions.
In one example, the codes are binary codes, and each code represents the tags used during a particular stage of synthesis of members of a combinatorial library.
The invention provides a method for the production of a combinatorial library of compound of general formula (I) using solid phase methodologies.
A method of rFVIII binding assay using the peptides deduced from a combinatorial library in a filtration plate process is described.
In a preferred embodiment, the method is used for rapidly screening member compounds of a combinatorial library for potential biological activity.
The invention enables simultaneous identification of proteins with or without prior purification, and makes it possible to select members of combinatory banks which interact with said proteins.
Provided herein are combinatorial containing chimeric Major Histocompatibility Comples (MHC) Class I proteins displayed on the surfaces of recombinant yeast cells.
A combinatorial library comprising a plurality of members represented by formula (a), is disclosed in which (b) is a solid support and -Z is a compound residue.
Mapping coordinates for a training subset of products in the combinatorial library, and features of their building blocks, are obtained.
In order to expediently synthesize a combinatorial library of derivatives based upon these core structures, a general methodology for the solid phase synthesis of these derivatives is also provided.
The method involves contacting the ligand with a combinatorial library of oligomers composed of morpholino subunits with a variety of nucleobase and non-nucleobase side chains.
Requêtes fréquentes français :1-200, -1k, -2k, -3k, -4k, -5k, -7k, -10k, -20k, -40k, -100k, -200k, -500k, -1000k,
Requêtes fréquentes anglais :1-200, -1k, -2k, -3k, -4k, -5k, -7k, -10k, -20k, -40k, -100k, -200k, -500k, -1000k,
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