Theoretical analyses of glibenclamide-estradiol derivative and its relationship with some physico-chemical descriptors

L. Figueroa-Valverde, F. Díaz-Cedillo, M. López-Ramos, E. García-Cervera, E. Pool Góme

Research output: Contribution to journalArticlepeer-review

2 Scopus citations

Abstract

A new glibenclamide-estradiol conjugate was synthesized by the reaction of glibenclamide-succinate and estradiol-ethylenediamine derivative using N,N'-diciclohexylcarbodiimide/p-toluensulfonic acid as catalysts. In order to evaluate the degree of lipophilicity and its relationship with some physicochemical descriptors involved in its chemical structure, the ACD log P and KOWWIN methods were used. The results showed an increase in the values of these physicochemical parameters for the glibenclamide-estradiol conjugate in comparison with glibenclamide and glibenclamide-succinate. These data suggest a relationship between the evaluated physicochemical parameters and the degree of lipophilicity of the glibenclamide-estradiol conjugate.

Original languageEnglish
Pages (from-to)1405-1409
Number of pages5
JournalAsian Journal of Chemistry
Volume25
Issue number3
StatePublished - 2013

Keywords

  • Estradiol
  • Glibenclamide
  • Lipophilicity

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