Skip to content
2000
Volume 16, Issue 12
  • ISSN: 0929-8665
  • E-ISSN: 1875-5305

Abstract

A series of Val-Leu based peptidic aldehydes containing either a furan or thiophene at the Nterminus was prepared and assayed against ovine m-calpain. In general, potency is favoured by a 2- substituted (rather than 3-substituted) heterocycle, a thiophene rather than a furan, and a shorter chain length at the N-terminus. Molecular docking experiments provide some rationale for these observations.

Loading

Article metrics loading...

/content/journals/ppl/10.2174/092986609789839296
2009-12-01
2025-09-29
Loading full text...

Full text loading...

/content/journals/ppl/10.2174/092986609789839296
Loading

  • Article Type:
    Research Article
Keyword(s): Calpain inhibitors; heterocycles; peptidic aldehydes; synthesis
This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error
Please enter a valid_number test