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112913-64-1

Articles about 112913-64-1Total 3 be found

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Site-Specific Incorporation of Multiple Thioamide Substitutions into a Peptide Backbone via Solid Phase Peptide Synthesis
Among various peptide modification strategies, thioamide substitution by replacing the carbonyl oxygen atom of an amide bond with a sulfur atom constitutes an invaluable tool for chemical biology, for use in peptide drug discovery and protein structure-fu
Yang, Jinhua,Wang, Changliu,Yao, Chaochao,Chen, Chunqiu,Hu, Yafang,He, Guifeng,Zhao, Junfeng
p. 1484 - 1494
(2020/01/02)

SOLUTION PHASE ROUTES FOR WNT HEXAPEPTIDES
The present disclosure relates generally to the field of polypeptide synthesis, and more particularly, to the solution phase synthesis of the Wnt hexapeptide Foxy-5 and protected derivatives and peptide fragments thereof.
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Page/Page column 19

(2020/12/30)

Acid-labile protecting groups for the synthesis of lipidated peptides
Lipidated peptides and their neolipoprotein derivatives are efficient tools for the investigation of biological processes in molecular detail. These compounds are often acid- and base-labile, and their synthesis requires the use of a combination of blocki
Kadereit, Dieter,Deck, Patrick,Heinemann, Ines,Waldmann, Herbert
p. 1184 - 1193
(2007/10/03)

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Chemical Properties

Density: 1.39±0.1 g/cm3(Predicted)
Storage Temp.:Store at 0°C
PKA: 9.94±0.46(Predicted)
PSA: 127.31000
LogP: 3.58280

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