A one-bead, one-stock solution approach to chemical genetics: part 2. (Q30783997)

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5 December 2019

title

A one-bead, one-stock solution approach to chemical genetics: part 2 (English)

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5

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5 December 2019

Randall King

6

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5 December 2019

author name string

P A Clemons

1

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5 December 2019

A N Koehler

2

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5 December 2019

B K Wagner

3

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5 December 2019

T G Sprigings

4

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5 December 2019

S L Schreiber

7

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5 December 2019

M A Foley

8

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5 December 2019

publication date

1 December 2001

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5 December 2019

published in

Chemistry and Biology

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5 December 2019

volume

8

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5 December 2019

issue

12

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5 December 2019

page(s)

1183-1195

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Small molecule inhibitor of mitotic spindle bipolarity identified in a phenotype-based screen

5 December 2019

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Target-oriented and diversity-oriented organic synthesis in drug discovery

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Solid Phase Peptide Synthesis. I. The Synthesis of a Tetrapeptide

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High-throughput screening of small molecules in miniaturized mammalian cell-based assays involving post-translational modifications

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Split--pool synthesis of 1,3-dioxanes leading to arrayed stock solutions of single compounds sufficient for multiple phenotypic and protein-binding assays

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A single-bead decode strategy using electrospray ionization mass spectrometry and a new photolabile linker: 3-Amino-3-(2-nitrophenyl)propionic acid

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7 January 2021

An alkylsilyl-tethered, high-capacity solid support amenable to diversity-oriented synthesis for one-bead, one-stock solution chemical genetics

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7 January 2021

A one-bead, one-stock solution approach to chemical genetics: part 1

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7 January 2021

Studies with trialkylsilyltriflates: new syntheses and applications

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Linkers and Cleavage Strategies in Solid-Phase Organic Synthesis and Combinatorial Chemistry

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7 January 2021

Selective Deprotection of Silyl Ethers

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7 January 2021

Exploiting site-site interactions on solid support to generate dimeric molecules

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7 January 2021

A Combinatorial Approach to Polyketide-Type Libraries by Iterative Asymmetric Aldol Reactions Performed on Solid Support We thank the European Commission (TMR Network ERB-FMR XCT 96-0011 and IHP Network HPRN-CT-2000-00014), EPSRC, Pfizer, and Merck

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7 January 2021

A versatile synthetic dimerizer for the regulation of protein–protein interactions

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7 January 2021

Asymmetric Catalysis in Diversity-Oriented Organic Synthesis: Enantioselective Synthesis of 4320 Encoded and Spatially Segregated Dihydropyrancarboxamides We thank the National Institute of General Medical Sciences (GM-52067) for support of this res

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7 January 2021

Decoding Products of Diversity Pathways from Stock Solutions Derived from Single Polymeric Macrobeads H.E.B. and L.P. contributed equally to this work. We thank the National Institute of General Medical Sciences (GM-52067) for the support of this re

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7 January 2021

10.1016/S1074-5521(01)00086-2

Identifiers

DOI

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5 December 2019

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