Semi-synthetic heparinoids

14Citations
Citations of this article
5Readers
Mendeley users who have this article in their library.
Get full text

Abstract

New chemical-enzymatic technology based on the modification of the bacterial polysaccharide K5 from Escherichia coli leads to the synthesis of a number of heparin/heparan sulfate-like molecules with different biological activities. With this technology, two families of sulfated compounds were synthesized, which differ in their uronic acid content. The first group contains only glucuronic acid, whereas the second group contains about 50% iduronic acid following epimerization by immobilized recombinant C5 epimerase. This has led to the development of various anticoagulant and nonanticoagulant K5 derivatives endowed with different - and sometimes highly specific - antitumor, antiviral, and/or anti-inflammatory activities. © 2012 Springer-Verlag Berlin Heidelberg.

Cite

CITATION STYLE

APA

Oreste, P., & Zoppetti, G. (2012). Semi-synthetic heparinoids. Handbook of Experimental Pharmacology, 207, 403–422. https://doi.org/10.1007/978-3-642-23056-1_18

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free