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A study of some thiol ester hydrolyses as models for the deacylation step of papain-catalysed hydrolyses

1. The self-catalysed hydrolyses of the thiol esters, S-hippurylthioglycollic acid and S-ethyl monothiolsuccinate, have been shown to be slower than the deacylation step for the papain-catalysed hydrolysis of hippuric esters, by a factor approx. 10(5). This difference in rate constants largely refle...

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Hlavní autoři: Lowe, G., Williams, A.
Médium: Artigo
Jazyk:Inglês
Vydáno: 1965
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1206921/
https://ncbi.nlm.nih.gov/pubmed/14343130
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