| Literature DB >> 27400366 |
Melissa J MacDonald1, Luke D Lavis2, Donald Hilvert3, Samuel H Gellman1.
Abstract
Efficient hydrolysis of amide bonds has long been a reaction of interest for organic chemists. The rate constants of proteases are unmatched by those of any synthetic catalyst. It has been proposed that a dipeptide containing serine and histidine is an effective catalyst of amide hydrolysis, based on an apparent ability to degrade a protein. The capacity of the Ser-His dipeptide to catalyze the hydrolysis of several discrete ester and amide substrates is investigated using previously described conditions. This dipeptide does not catalyze the hydrolysis of amide or unactivated ester groups in any of the substrates under the conditions evaluated.Entities:
Year: 2016 PMID: 27400366 DOI: 10.1021/acs.orglett.6b01279
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005