Physicochemical aspects of the enzymatic hydrolysis of carboxylic esters

Peter Buchwald, N. Bodor

Research output: Contribution to journalArticle

22 Citations (Scopus)

Abstract

Considering the important role played by enzymatic hydrolysis in the metabolism of therapeutic agents designed by retrometabolic approaches (soft drugs and chemical delivery systems), the present article offers a review of a number of issues related to the enzymatic hydrolysis of carboxylic esters. Current knowledge regarding interorgan- and interspecies variability, stereospecificity, activation energy, proposed mechanism, and quantitative structure-metabolism relationship is summarized. The effects of chain-length and branching in the alcohol or acyl substituent on the rate of hydrolysis in congener series are also summarized. Available in vitro human blood data suggest that shortest half-lives are achieved with sterically non-hindered chains that are neither too short nor too long and are of around four carbon-atom long.

Original languageEnglish
Pages (from-to)87-93
Number of pages7
JournalPharmazie
Volume57
Issue number2
StatePublished - Feb 26 2002
Externally publishedYes

Fingerprint

Enzymatic hydrolysis
Metabolism
Esters
Hydrolysis
Chain length
Blood
Carbon
Activation energy
Alcohols
Drug Delivery Systems
Atoms
Pharmaceutical Preparations
Therapeutics

ASJC Scopus subject areas

  • Drug Discovery
  • Organic Chemistry
  • Chemistry(all)
  • Molecular Medicine
  • Pharmacology
  • Pharmaceutical Science

Cite this

Physicochemical aspects of the enzymatic hydrolysis of carboxylic esters. / Buchwald, Peter; Bodor, N.

In: Pharmazie, Vol. 57, No. 2, 26.02.2002, p. 87-93.

Research output: Contribution to journalArticle

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