The stereochemical specificity of esterases
- 1 January 1930
- journal article
- research article
- Published by Portland Press Ltd. in Biochemical Journal
- Vol. 24 (1), 190-198
- https://doi.org/10.1042/bj0240190
Abstract
The levo-forms of methyl-n-hexyl-carbinol, methylphenylcarbinol and methyl-b-phenylethylcarbinol inhibited sheep-liver es-terase more strongly than the dextro-forms. The es-terase of rabbit-liver did not show this selective affinity.This publication has 1 reference indexed in Scilit:
- Molecular constitution and accessibility to enzymesBiochemical Journal, 1929