期刊
ACS COMBINATORIAL SCIENCE
卷 20, 期 2, 页码 61-69出版社
AMER CHEMICAL SOC
DOI: 10.1021/acscombsci.7b00169
关键词
one bead one compound library; combinatorial chemistry; cyanoacrylamide; covalent; reversible; Knoevenagel condensation; DNA; DNA-encoded library
资金
- National Institutes of Health [AG 054892]
- Klorfine Foundation
We demonstrate that the Knoevenagel condensation can be exploited in combinatorial synthesis on the solid phase. Condensation products from such reactions were structurally characterized, and their Michael reactivity with thiol and phosphine nucleophiles is described. Cyanoacrylamides were previously reported to react reversibly with thiols, and notably, we show that, dilution into low pH buffer can trap covalent adducts, which are isolable via chromatography. Finally, we synthesized both traditional and DNA-encoded one-bead, one-compound libraries containing cyanoacrylamides as a source of cysteine-reactive reversibly covalent protein ligands.
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